Disruption of astrocyte-vascular coupling and the blood-brain barrier by invading glioma cells

Abstract

Astrocytic endfeet cover the entire cerebral vasculature and serve as exchange sites for ions, metabolites, and energy substrates from the blood to the brain. They maintain endothelial tight junctions that form the blood-brain barrier (BBB) and release vasoactive molecules that regulate vascular tone. Malignant gliomas are highly invasive tumors that use the perivascular space for invasion and co-opt existing vessels as satellite tumors form. Here we use a clinically relevant mouse model of glioma and find that glioma cells, as they populate the perivascular space of pre-existing vessels, displace astrocytic endfeet from endothelial or vascular smooth muscle cells. This causes a focal breach in the BBB. Furthermore, astrocyte-mediated gliovascular coupling is lost, and glioma cells seize control over regulation of vascular tone through Ca²⁺-dependent release of K⁺. These findings have important clinical implications regarding blood flow in the tumor-associated brain and the ability to locally deliver chemotherapeutic drugs in disease.

Introduction

It is now well established that astrocytes play important roles in supporting normal brain function¹. This is largely accomplished by astrocytic processes that form endfeet covering ∼99% of the cerebral vascular surface². Astrocyte endfeet, in conjunction with pericytes³, help to maintain the expression of endothelial tight junction proteins, transporters, and enzymes, which together comprise the blood-brain barrier (BBB)^{4, 5, 6}. Additionally, astrocytes can release a number of vasoactive molecules from their endfeet onto the underlying vascular smooth muscle cells, regulating vascular tone⁷. This process, called functional hyperemia or neurovascular coupling (NVC), adjusts local cerebral blood flow (CBF) to match regional neuronal energy demand. NVC is accomplished by translating neuronal activity into increases in astrocytic [Ca²⁺]_i, which causes the generation and/or release of several vasoactive molecules including the arachidonic acid metabolites epoxyeicosatrienoic acids (EETs), prostaglandin E₂ (PGE₂), and 20-HETE, or K⁺. These metabolites act on smooth muscle cells lining cerebral arterioles causing them to dilate or constrict^{7, 8, 9, 10, 11}.

Primary glial-derived brain tumors, gliomas, are highly invasive cancers, which often migrate along existing brain structures including white matter tracks and blood vessels^{12, 13}. Endothelial-derived bradykinin initially attracts glioma cells to the vasculature¹⁴ and the extracellular matrix surrounding these blood vessels is enriched with molecules, such as fibronectin and vitronectin, that promote cell migration¹⁵. Interactions of glioma cells with the vasculature occurs in three distinct ways: 1) perivascular invasion of migrating glioma cells along the pre-existing vasculature and 2) co-option of pre-existing host vessels¹⁶ during initial tumor growth or by small satellite tumors. As the disease progresses and the tumor mass grows, co-opted vessels eventually undergo apoptosis and 3) angiogenesis is induced by the release of angiogenic molecules such as vascular endothelial growth factor (VEGF) ¹⁷ at the fringe of the tumor mass. In this study, we exclusively focused on the interaction of migrating glioma cells with the preexisting vasculature outside of the main tumor mass.

Given the extensive coverage of cerebral vessels by astrocytic endfeet², we asked whether gliomas invading along or co-opting vessels might alter astrocyte-vascular interactions at the pre-existing vasculature. Using several clinically relevant mouse models of glioma, we show that a vast majority of human glioma cells that traveled outside of the main mass associate with blood vessels and insert themselves between the endfoot and the endothelial wall of the preexisting blood vessel, confirming previous reports using rodent glioma cell lines^{13, 18, 19}. The loss of contact between endfeet and blood vessels leads to a loss of tight junctions thereby causing a focal breach of the BBB allowing blood-borne molecules to enter the brain parenchyma even far away from the main tumor mass. Furthermore, the physical dislocation of astrocytes from the blood vessels and subsequent encasing of vessels by gliomas disrupts astrocyte-vascular coupling. Importantly, single glioma cells are sufficient to locally open the BBB and focally disrupt gliovascular coupling. These findings have important clinical implications regarding blood flow in the tumor-associated brain and the ability to locally deliver chemotherapeutic drugs in disease.

Results

Glioma cells associate with blood vessels

Gliomas interact with both existing and newly generated blood vessels at different stages of the disease. Early on, existing vessels serve as a pathway for tumor invasion²⁰. Later, new vessels generated through angiogenesis²¹, supply blood-borne nutrients to support tumor growth. This period is preceded by vascular co-option where gliomas form cuff-like clusters around resident vessels¹⁸. Perivascular invasion and vascular co-option continue throughout the disease as tumor cells spread and create satellite tumors. The principle objective of this study was to study the interaction of gliomas with the existing vasculature.

To do so, we used mouse models of glioma that replicate salient features of the disease including perivascular invasion²⁰, vascular co-option^{16, 18} and angiogenesis¹⁷. As a first step, we investigated the extent to which glioma cells associate with blood vessels, paying specific attention to vessel type and size. To visualize tumor cells in brain, we implanted eGFP-expressing human glioma cells (D54-eGFP) into the cortex of immunodeficient scid mice and allowed cells to proliferate and invade for 2-4 weeks. Almost all D54 glioma cells, outside of the main tumor mass, associate with CD31 (PECAM-1)-labeled blood vessels (Fig. 1a). To assure that this phenomenon is a general property of glioma cells, we generated gliomas using 4 additional glioma sources; one mouse-derived glioma cell line (Gl261-dsRed) and 3 different patient-derived glioma xenolines (GBM22, GBM39 and GBM14). The latter tissue has been exclusively propagated in the flanks of nude mice to preserve protein expression of the original tumor²². As with D54 glioma cells, the mouse- and patient-derived tumor cells that migrated into the parenchyma were frequently associated with blood vessels (Fig. 1 b, c; Supplementary Fig. 1). For further studies, we focused on D54-eGFP cells, as well as GBM22 (classified as mesenchymal subtype) and GBM14 (classified as classical subtype). Similarly to D54 gliomas, GBM22 gliomas form loose tumor borders with cells invading chain-like into the parenchyma using blood vessels as a scaffold (Fig. 1b; Supplementary Fig. 1e,f). In each preparation, the vast majority of cells contact a vascular surface (Fig. 1d-f).

Figure 1. Glioma cells can associate with blood vessels of all sizes and types.

Immunofluorescence of CD31 (PECAM) and eGFP-expressing human glioma cells (D54) (a) or patient-derived xenograft lines GBM22 (b) and GBM14 (c) implanted in the cerebrum of immunodeficient mice highlighting the high number of invading glioma cells found along the vasculature. To be scored “vessel-associated” we required overlap of pixels of the endothelial cell (red) and the tumor cell (green) label in 1 to 2 um single planes of confocal images. Only a minority of cells is not found along the vasculature (d-f, arrow heads). Perivascular glioma cells can associate with capillaries (<7 μm) (g), penetrating arterioles or venules (7-35 μm) (h), and large arteries or veins (>35 μm) (i). Quantitative analysis based on 1634 cells in 5 random sections from each slice and 3 slices from 4 different animals (j). Immunofluorescence of Alexa Fluor 633 hydrazide dye (633 hyd, white) and eGFP-expressing astrocytes (Aldh1l1-eGFP) or human glioma cells (D54) implanted in the cerebrum of immunodeficient mice allowing to distinguish arterioles/arteries from venules/veins and capillaries (k-m). Black font was used to describe white labels in confocal images. Quantification of 75 sections from 4 tumor-bearing animals show that glioma cells associate with every type of vessel (j). In vivo visualization of eGFP-expressing human- glioma cells implanted in the cerebrum of immunodeficient mice found invading along the vasculature outlined by tetramethylrhodamine-dextran (TRITC-dex). Arterioles show divergent and venules show convergent blood flow at branch points (arrows in k,o,p). Perivascular glioma cells can associate with capillaries (n), penetrating arterioles (o), penetrating venules (p). Scale, 20 μm. Statistical data: a,d n=4 animals; b n=5 animals; c n=7 animals; f quantification for n=4 D54 animals, n=3 GBM22 and GBM14 animals; g-m n=9 animals; n-p n=34 animals.

Most D54 glioma cells associated with capillaries (<7 μm diameter), which accounted for 47.5 % of the total vessel area. About one third of the cells were attached to penetrating arterioles or collecting veins (7-35 μm diameter, 51 % of the total vessel area). Only few cells contacted large arteries or veins (>35 μm diameter) (Fig. 1g-j), which represented only 1.6 % of the total vessel area measured. Thus, while the low occupancy of large vessels reflects the low occurrence of these vessels, there might be a preference of glioma cells for capillaries over arterioles/venules.

Next, we asked whether glioma cells preferentially associate with vessels carrying arterial as opposed to venous blood. Arteries (35-100 μm) and arterioles (7-35 μm) contain contractile vascular smooth muscle cells (VSMCs) that regulate vascular tone, and larger arteries have an internal elastic lamina^{23, 24}. Cerebral venules and large veins lack VSMCs and the ability to actively constrict and dilate. All vessels are non-selectively labeled with the endothelial marker CD31 (Fig. 1a-i). To identify arterioles/arteries, we used either alpha-smooth muscle actin (αSMA), present in the VSMCs, or Alexa Fluor 633 hydrazide dye, which binds to the elastin found only in arteries/arterioles equal or greater than 10 μm in diameter²⁵. Representative examples of each vessel type associated with glioma cells are depicted in Fig. 1g-I, k-m and Fig. 2a-c. Quantitative analysis showed 54.46% covering venules/veins over 10 μm and 36.28% associating with arterioles/arteries over 10 μm (Fig. 1j). For the 9.25% of vessels between 7 and 10 μm, we were unable to differentiate between arterioles and venules since they lack elastin that is bound by the hydrazide dye (Fig. 1j).

Figure 2. Perivascular glioma cells can displace astrocytic endfeet along the vasculature.

Immunofluorescence of CD31 (PECAM), aquaporin-4 (AQ4) and eGFP-expressing human glioma cells (D54) implanted in the cerebrum of immunodeficient mice show displacement of the astrocyte endfeet by tumor cells from the vessels in general (a) and from arterioles/arteries labeled with either alpha smooth muscle action (αSMA) (b) or Alexa Fluor 633 hydrazide (633 hyd) (c). This could be confirmed by implanting patient-derived xenograft tumors labeled with Human Nuclei (HuN) (d) or TdTomato-expressing human glioma cells (D54) (e) into the cerebrum of Aldh1l1-eGFP immunodeficient mice allowing visualization astrocyte endfeet independent of AQ4 expression. Perivascular glioma cells can intercalate between endothelial cells and astrocytic endfeet (a,c) or completely displace the astrocytic endfoot from the vascular surface (b). Electron microscopy (g-i) shows that perivascular astrocytes (brown) are less electron-dense than perivascular human glioma cells (green), which can displace astrocytic endfeet, allowing for physical contact with the endothelial cell (g-i) or can sometimes sit on top of astrocyte endfeet (i). Black font was used to describe white labels in confocal images. See panel f for quantification (n=34 vessels for D54; n=44 for GBM22; n=38 for GBM14). Scale, 20 μm (a-e); 2 μm (g), 4 μm (h,i). Statistical data: a-c n=18 animals; d n=12; e n=5 animals; g n=3 animals, h n=2 animals, i n=2 animals.

To complement these studies we also assessed vessel preference of invading glioma cells in vivo by two-photon imaging. A craniotomy was performed in tumor-implanted mice and the vasculature was highlighted by tail vein injection of tetramethylrhodamine (TRITC)-dextran. The direction of blood flow and size of vessel was used to identify the vessel type; arterioles show divergent and venules show convergent blood flow at branch-points (Fig. 1n-p). Taken together these studies suggest that a vast majority of gliomas associate with blood vessel along the entire vascular tree with a clear preference for small caliber capillaries.

Glioma cells displace astrocyte endfeet from the vasculature

The brain's vascular surface is over 99% covered by astrocytic endfeet², which are anchored to the basement membrane of the endothelial cells via integrin, dystroglycan and agrin⁶ leaving only a minute Virchow-Robin space filled with interstitial fluid that is part of the “glymphatic” system²⁶. Hence, as glioma cells invade along blood vessels astrocytic endfeet may pose an obstacle to cell movement. To examine the physical relationship between endfeet, gliomas, and blood vessels, we used cell type specific markers on histological sections. As illustrated in Fig. 2, the normal interaction between the astrocytic endfoot and vasculature is frequently disrupted by the presence of perivascular glioma cells either by the physical displacement of the astrocytic endfoot labeled with aquaporin-4 (AQ4) (Fig. 2a,c) or by the elimination of the endfoot altogether (Fig. 2b), presumably through process retraction as previously reported¹⁹. To ensure that the latter was not due to a loss of AQ4 protein in the membrane, we repeated these studies using an immunodeficient reporter mouse with expression of eGFP under the astrocyte-specific Aldh1l1 promoter and tumor cells either expressing the red fluorescent TdTomato (D54) or detected by antibody staining against HuN (GBM). Immunohistochemistry from these animals again show that glioma cells indeed displaced the astrocytic endfoot away from the vasculature and are in direct contact with endothelial cells (Fig. 2d,e, Supplementary Fig. 2). As expected, vessels not occupied by glioma cells remain covered by astrocytic endfeet (Supplementary Fig. 2c).

To study the displacement of astrocytic endfeet by individual glioma cells at even higher resolution we employed electron microscopy (EM) (Fig. 2g-i, Supplementary Fig. 3-5). Criteria for the distinction of glioma cells and astrocyte processes included the different electron densities of glioma cells and astrocytes (Supplementary Fig. 4e). A higher electron density and hence darker appearance of the glioma cytoplasm is due to a rougher endoplasmic reticulum²⁷. Glioma cells also showed a high nucleus to cytoplasm ratio with large often convoluted or segmented nuclei and multiple nucleoli. Euchromatin is more abundant than heterochromatin resulting in an even higher electron density of the glioma nucleus²⁸. In contrast, astrocyte endfeet are characterized by a less electron-dense (lighter) cytoplasm with internal substructures of filamentous networks and bundles of glial filaments²⁹ (Supplementary Fig. 4e). We found glioma cells, distinguished from astrocytes by increased electron-density and enlarged nuclei (Fig. 2g-i, Supplementary Fig. 3-5, confirmed by a clinical pathologist), displacing the astrocyte endfeet from the endothelial wall in a majority of the analyzed vessels of D54-, GBM22- and GBM14-implanted mice (Fig. 2f-i, see Supplementary Fig. 3-5 for additional examples and quantification). However, on some vessels glioma cells were in close proximity of the vessel wall, but still separated by the astrocytic endfeet (Fig. 2f,i, Supplementary Fig. 5f). Taken together these studies illustrate that glioma cells can gain direct access to the abluminal side of cerebral vessels through the displacement of astrocytic endfeet.

Vessel co-option by glioma cells breaches the BBB

Development of the BBB precedes astrocyte development and is induced by pericytes^{30, 31}, yet maintenance of an intact barrier relies on soluble factors released by astrocytes and persistent contact between astrocytes and endothelial cells^{5, 32}. Accordingly, pathological conditions that compromise astrocytes also present with an impaired BBB⁴. A leaky BBB is also typical for newly generated glioma vasculature, which lacks tight junctions³³. This can be readily demonstrated by permeation of Evan's blue from the bloodstream into the brain parenchyma surrounding a large tumor mass (Fig. 3a).

Figure 3. Perivascular glioma cell co-option causes a breakdown of the blood-brain barrier.

The tracer, Evans blue, permeates into the brain parenchyma in tumor-bearing (n=3 animals) (bottom), but not in sham mice 3 weeks post surgery (n=3 animals) (top), Scale 5 mm. (a). Immunofluorescence of CD31 and intravenously injected tracers, tetramethylrhodamine-albumin (TRITC-alb, white) or -cadaverine (TRITC-cad, white), and implanted eGFP-expressing human glioma cells (D54) allow analysis of tracer leakage in relation to tumor burden. The large MW 70 kDa TRITC-albumin (b), as well as the small MW 950 Da TRITC-cadaverine (d) can be found outside the vasculature (arrows) (b-f, Suppl. Fig.6). Note that leaked TRITC-cadaverine is taken up by nearby neurons (arrows) (d,e). No extravasation was seen in the absence of tumor cells (c,f). To assess extravasation of the tracer Cascade blue (MW 10 kDa), Aldh1l1-eGFP-scid (eGFP) immunodeficient mice, which were previously implanted with TdTomato-expressing human glioma cells (D54), were retro-orbitally injected with Alexa Fluor 633 hydrazide dye (633 hyd) and Cascade blue (g,h). Accumulation of Cascade blue occurs in the brain's parenchyma indicating breakdown of the blood-brain barrier (BBB), where perivascular astrocytes have been displaced by glioma cell co-option (g). Vessels lacking tumor cells do not show extravasation of the dye (h). Immunohistochemistry for the TJ proteins zonula occludens-1 (ZO-1) (i) and claudin-5 (k) show that these protein are lost from endothelial cells labeled with CD31 where tumor cells are present (enlarged panel, arrows), but colocalize with endothelial cells in tissue that has not been co-opted. Quantification of ZO-1 shows reduction of vessel coverage in areas co-opted by glioma cells. 8.86 ± 0.64% vessel area is covered by ZO-1 in control images, whereas this number was reduced to 5.1 ± 1.11% in areas where vessels were coopted by tumor cells (n=9 images each for control and tumor-covered vessels from 3 animals, paired t-test directly comparing control and tumor images in the same slice, p=0.037, error bars refer to SEM) (j). Black font was used to describe white labels in confocal images. Scale 20 μm. Statistical data: b,c n=10 animals; d-f n=7 animals; g n=2 animals; h n=4 animals; i,k n=6 animals.

In light of the demonstrated displacement of astrocytes by perivascular glioma cells, we asked if focal disruption of the normal astrocyte-endothelial cell interactions along existing vessels was sufficient to breach the BBB. Therefore, we examined the leakage of TRITC-albumin (MW 70 kDa) from blood vessels distant from the D54-tumor mass and associated with only few glioma cells. As expected, the main tumor mass, where angiogenesis leads to the formation of naïve and leaky immature microvessels, showed extensive extravasation of the TRITC-albumin from the vasculature (Supplementary Fig. 6). However, even at distant sites where vessels were associated with only small groups of cells or even just a single glioma cell, the dye was still found outside the lumen of the vasculature suggesting a focal breach of the BBB (Fig. 3b). Surprisingly just a few cells were sufficient to cause albumin leakage. No leakage was observed in cortical areas lacking tumor in the same animal (Fig. 3c). We obtained similar results with a second, much smaller, permeability marker, TRITC-cadaverine (MW 950 Da) that is taken up by surrounding neurons³⁰ (Fig. 3d,e). Again, no leakage was observed in glioma-free vessels in the same animals (Fig. 3f). Animals intracranially implanted with non-malignant primary mouse glial cells obtained from Aldh1l1-eGFP-scid mice were retro-orbitally injected with cadaverine-Alexa555, Evans blue and albumin-Alexa555 3, 7 and 14 days later. Dye leakage was restricted to the area surrounding the needle tract at all time points and decreased over time suggesting that the injury inflicted by the needle healed and non-malignant glial cells do not cause breach of the BBB (Supplementary Fig. 7).

We also examined BBB integrity in vivo, using a 10 kDa permeability marker, cascade blue, injected retro-orbitally. Two photon imaging revealed clouds of cascade blue emanating from vessels where invading gliomas had displaced the astrocytic endfeet (Fig. 3g, Supplementary Fig. 6c), yet no leakage was observed along glioma free vessels (Fig. 3h).

Endothelial tight junctions (TJs) form the physical barrier limiting diffusion of blood-born molecules into the brain's parenchyma and are characterized by the presence of proteins such as zonula occludens-1 (ZO-1) and claudin-5. The presence of single tumor cells can reduce the expression of ZO-1 (Fig. 3i,j). Similarly, claudin-5 is abundant along vessels lacking tumor cells, but is largely diminished where tumor cells contact the vasculature (Fig. 3k). Taken together, these data suggest that the focal displacement of an astrocyte endfoot by a single or few glioma cells is sufficient to open the BBB presumably through a loss of TJs.

Glioma cells cause loss of astrocyte-vascular coupling

Release of vasoactive molecules by astrocytic endfeet onto blood vessels, also called gliovascular coupling, causes local changes in cerebral blood flow in response to neuronal activity⁷. Specifically, activation of astrocytic G-protein coupled receptors (GPCRs) causes an increase in [Ca²⁺]_i, and activation of phospholipase A₂, which converts membrane phospholipids into arachidonic acid (AA). AA can be either released from the astrocyte to be converted into 20-HETE in the VSMC causing vasoconstriction or metabolized into PGE₂, which dilates vessels. Ca²⁺ is the cellular signal that precedes a vessel diameter change and the type of response, dilation or constriction, can be modulated by the brain's metabolism³⁴ (Schematically depicted in Fig. 8).

Figure 8. Perivascular glioma cells disrupt astrocyte-mediated vascular coupling.

The perivascular glioma cell (green) inserts itself between the vascular smooth muscle cells (VSMCs) (blue) surrounding the vascular endothelial cells (red), displacing the astrocytic endfoot (purple). Bath application of norepinephrine (NE) and trans-ACPD (t-ACPD) activates astrocytic G-protein coupled receptors causing an increase in astrocytic [Ca²⁺]_i. Due to perivascular glioma cell displacement of the astrocytic endfoot, astrocyte-released vasoactive molecules (arachidonic acid (AA), prostaglandin E₂ (PGE₂), and K⁺) can no longer reach the VSMCs to cause alterations in vessel diameter. Glioma cell-protease activated receptor 1 (PAR1) activation by the artificial ligand, TFLLR, causes increases in glioma cell [Ca²⁺]_i, which activates Ca²⁺-activated K⁺ channels. Glioma efflux of K⁺ onto VSMCs causes vasoconstriction of arterioles.

Central to astrocyte-mediated control of blood flow is the presence of endfeet on the vasculature. Since we found astrocytic endfeet along arterioles frequently displaced from the VSMCs by perivascular glioma cells (Fig. 2b,c; Fig. 3g, Supplementary Fig. 2-5), we questioned whether vascular coupling was altered. To answer this, we first used a pharmacological approach to selectively stimulate astrocytes and assessed responses of arterioles. We bath applied two drugs known to selectively increase [Ca²⁺]_i in astrocytes, namely trans-ACPD and norepinephrine (NE)^{11, 34, 35} to acute brain slices and measured the vessel diameter change by video-microscopy for arterioles identified by a thickened vessel wall indicating the presence of a VSMC layer with D54 ((+)Tumor cell(s)) or without perivascular glioma cells ((-)Tumor cell(s)). For all experiments, diameter changes in response to trans-ACPD and NE were assessed at high (95%) and low (20%) oxygen concentrations as these oxygen concentrations have been shown to cause opposite vascular responses due to the limitation of 20-HETE and nitric oxide production by limited oxygen amounts^{7, 34}. In agreement with previous studies^{11, 34}, application of trans-ACPD caused vasodilatation (O₂^low, n=12) or vasoconstriction (O₂^high, n=20) in tumor-free vessels (Fig. 4a-c). Similarly, NE application induced constriction (O₂^high, n=18) or dilation (O₂^low, n=22) in glioma-free arterioles (Fig. 4d-f). In contrast, arterioles encased by glioma cells showed a significant decrease in vessel response after trans-ACPD (O₂^low: n=9, two-tailed unpaired t-test, p=0.012; O₂^high: n=16, two-tailed Mann-Whitney test, p=0.0032) (Fig. 4a-c) or NE application (O₂^high: n=18, two-tailed unpaired t-test, p=0.0049; O₂^low: n=21, two-tailed unpaired t-test, p=0.01) (Fig. 4d-f).

Figure 4. Loss of astrocyte-vascular coupling following vessel co-option by gliomas.

(a) DIC images of vessels without (top) or with (bottom) perivascular glioma cells before and after application of 100 μM trans-ACPD (t-ACPD). Perivascular glioma cell presence was verified by eGFP-fluorescence. (b) Changes in vessel diameter for an arteriole associated (grey) and not associated (black) with perivascular glioma cells over the course of one experiment when exposed to 100 μM trans-ACPD (arrowhead). (c) Average change in vessel diameters observed at high (h) (95%) and low (l) (20%) oxygen for vessels associated (grey) and not associated (black) with glioma cells when exposed to 100 μM trans-ACPD. (d) DIC images of vessels without (top) or with (bottom) perivascular glioma cells before and after application of 10 μM norepinephrine (NE). Perivascular glioma cell presence was verified by eGFP-fluorescence. (e) Changes in vessel diameter for an arteriole associated (grey) and not associated (black) with perivascular glioma cells over the course of one experiment when exposed to 10 μM NE (arrowhead). (f) Average change in vessel diameters observed at high (h) (95%) and low (l) (20%) oxygen for vessels associated (grey) and not associated (black) with glioma cells when exposed to 10 μM NE. For experiments performed at low oxygen concentrations, arterioles were preconstricted with 125 nM U46619 for 20 min. Statistical data provided in results section, error bars refer to SEM. Scale, 20 μm.

Slices obtained from D54-GCaMP3-GFP tumors bearing a genetically encoded Ca²⁺ sensor showed no significant Ca²⁺ increase induced by trans-ACPD or NE in glioma cells (Supplementary Fig. 8a) assuring that the effects of both drugs are targeted to astrocytes as previously demonstrated^{11, 34, 35}.

To further ensure that the observed lack in vessel response is indeed due to diminished astrocyte-vascular coupling and not caused by unspecific effects of the drugs on other cell types, we stimulated single astrocytes surrounding vessels with or without glioma cells by uncaging [Ca²⁺]_i after loading acute brain slices of tumor-bearing animals with DMNPE-4 caged Ca²⁺³⁶. In control slices derived either from naïve animals or from brain regions devoid of tumor, uncaging Ca²⁺ corresponds to an increase in Ca²⁺ detected by the Ca²⁺-indicator dye Fluo-4, which was followed by either constriction or dilation of the nearby arteriole (Fig. 5a-c,g,h; Supplementary Movies 1,2).

Figure 5. Vascular responses to Ca²⁺ uncaging in astrocytes is impaired in vessels co-opted by glioma cells.

[Ca²⁺]_i uncaging in an astrocyte endfoot or cell body close to an arteriole free of glioma cells leads to either constriction (a) or dilation (c) of the vessel. The vessel response is preceded by a rise in [Ca²⁺]_i (b,d). The pink spot indicates the location of Ca2+ uncaging. Measurement of the Ca²⁺ response was performed in this region or in an immediate adjacent region. Vessels encased by glioma cells do not respond to Ca²⁺ uncaging in nearby astrocytes (e,f). Stimulation of astrocytes in tumor-free areas of the same vessel (downstream vessel area) causes constriction showing that the lack of response is specific for areas covered by glioma cells (f,g). The cumulative relative frequency distribution shows a wide range of dilatory or constricting vessel responses in controls, whereas most vessels associated with glioma do not respond or do so to a lesser extent (h). Statistical data in d: control dilating vessels, 60.05 ± 8.899 %, n=10 vessels, tumor dilating, 5.18 ± 1.493, n=8, two-tailed unpaired t-test, p ≤ 0.0001; control constricting vessels, -43.51 ± 6.283 % n=18 vessels, glioma constricting, -9.389 ± 2.611 %, n=9. two-tailed unpaired t-test, p≤ 0.001, error bars refer to SEM.

Scale, 20 μm.

This response occurred within seconds on a faster time scale than the response after drug application, which is likely due to the slow perfusion and diffusion of the drugs into the slice. In contrast, Ca²⁺ uncaging in astrocytes close to vessels co-opted by D54 glioma cells failed to respond (Fig. 5d-f,h) indicating that astrocyte-derived signals do not reach the vasculature. However, the same vessels responded if astrocytes were stimulated in areas that were not covered by glioma cells (Fig. 5f,g).

Taken together, these data show that the presence of perivascular glioma cells is sufficient to disrupt astrocyte mediated gliovascular coupling (Schematically depicted in Fig. 8).

Perivascular glioma cells do not compromise VSMC function

Although the above data suggests that the displacement of the astrocytic endfoot from the vessel is responsible for a loss of vasoregulation by astrocytes, it is also possible that the presence of glioma cells may have impaired the function of the arterial smooth muscle cells. To address this possibility, we compared vessel responses of arterioles associated and those not associated with glioma cells after bath application of drugs known to directly target VSMCs. We applied (a) the thromboxane A₂ agonist U46619, a stable synthetic analog of PGH₂, which constricts parenchymal arteries by binding to TXA₂ receptors on VSMCs^{8, 37, 38}, (b) K⁺, which produces significant vasoconstriction by activating VSMC voltage-dependent Ca²⁺ channels⁹, and (c) endothelin-1 (ET-1), a potent vasoconstrictor³⁹ released by vascular endothelial cells that binds to the endothelin receptor found on VSMCs. These three vasoconstrictive agents showed no significant difference whether applied to glioma-associated or glioma-free vessels (Fig. 6a,b).

Figure 6. Perivascular glioma cells do not compromise vascular smooth muscle cell function.

DIC images of vessels without (top) or with (bottom) perivascular glioma cells before and after application of 125 nM U46619. Perivascular glioma cell presence was verified by eGFP-fluorescence (a). Average change in vessel diameters observed at high (h) (95%) and low (l) (20%) oxygen for vessels associated (grey) and not associated (black) with glioma cells when exposed to 125 nM U46619, 60 mM [K⁺]_o, 10 nM ET-1 (b) and 1 μM PGE₂ (c). For 1 μM PGE₂, arterioles were preconstricted with 125 nM U46619 for 20 min. Statistical data as follows: 20% Oxygen. 125 nM U46619: (+)Tumor Cell(s) n=11, (-)Tumor Cell(s) n=11, two-tailed Mann Whitney Test, p=0.40; 60 mM [K⁺]_o: (+)Tumor Cell(s) n=10, (-)Tumor Cell(s) n=9, two-tailed unpaired t-test, p=0.57; 10 nM ET-1: (+)Tumor Cell(s) n=8, (-)Tumor Cell(s) n=9, two-tailed unpaired t-test, p=0.78; 1 μM PGE₂: (+)Tumor Cell(s) n=14, (-)Tumor Cell(s) n=21, two-tailed unpaired t-test, p=0.72. 95% Oxygen. 125 nM U46619: (+)Tumor Cell(s) n=14. (-)Tumor Cell(s) n=12, two-tailed unpaired t-test, p=0.99; 60 mM [K⁺]_o: (+)Tumor Cell(s) n=11, (-)Tumor Cell(s) n=19, two-tailed Mann-Whitney Test, p>0.9999; 10 nM ET-1: (+)Tumor Cell(s) n=7, (-)Tumor Cell(s) n=9, two-tailed unpaired t-test, p=0.48). Error bars refer to SEM Scale, 20 μm.

Similarly, the vasodilator prostaglandin E₂ (PGE₂), which binds receptors of the prostaglandin receptor family on VSMCs⁴⁰, dilated arterioles that were preconstricted with U46619 as previously described³⁴ with no significant difference whether gliomas were present or not (Fig. 6c). The lack of a difference in the responsiveness of these two populations of vessels suggests that the perivascular glioma cells do not affect the function of the VSMC.

Perivascular glioma cells assume control of vasculature tone

Once gliomas have displaced astrocytes from the vessel, they often completely encase the blood vessel (Figs. 1a, 2b,c). This begs the question of whether glioma cells are now also in a position to actively control vessel tone using the same or different mechanisms employed normally by astrocytes. Previous studies report a significant dilation of vessels within the main tumor mass²¹, which we could confirm in our animal models (Supplementary Fig. 9a,b). However, pre-existing vessels with glioma cells do not have significantly larger vessel diameters overall (Supplementary Fig. 9c). Nonetheless, glioma cells might regulate vascular tone upon stimulation.

To examine a potential glioma-mediated vascular regulation, we exploited both, Ca²⁺ photo-uncaging from glioma cells and the use of the protease-activated receptor 1 (PAR1). PAR1 is a GPCR that is highly expressed in glioma cells where its activation causes an increase in [Ca²⁺]_i⁴¹. Natural ligands for PAR1 include thrombin and plasmin⁴², both found within the vasculature. Bath application of the selective PAR1 agonist, TFLLR, to control or glioma-bearing brain slices did not cause a detectable increase in [Ca²⁺]_i in astrocytes (Supplementary Fig. 8c). Accordingly, arterioles lacking perivascular glioma cells (n=10) caused no change in vessel diameter (Fig. 7a-c, Supplementary Fig. 8b, Supplementary Movie 3). In contrast, in arterioles completely surrounded by perivascular glioma cells, TFLLR caused a significant vasoconstriction ((n=9), two-tailed unpaired t-test, p=<0.0001) (Fig 7a-c, Supplementary Movie 4). The use of GCamp3 expressing glioma cells allowed us to examine the temporal relationship of the PAR1-mediated Ca²⁺ increases and the ensuing vessel constriction for an increase in GFP-fluorescence corresponds to increases in [Ca²⁺]_i. A pronounced Ca²⁺ increase preceded vasoconstriction of the arteriole (Fig. 7b,c, Supplementary Movie 4), similar to previous reports in astrocytes³⁵. Accordingly, we could induce a vascular response by uncaging [Ca²⁺]_i in glioma cells that are in contact with arterioles (Fig. 7d,e, Supplementary Fig. 8c, Supplementary Movie 5). In cortical astrocytes, K⁺ release via Ca²⁺-activated BK channels has been shown to control cerebral blood vessels, dictating whether vasoconstriction or vasodilation occurs depending on the resulting extracellular concentration of K^{+8, 9}. Glioma cells abundantly express two Ca²⁺-activated K⁺ channels, BK and IK^{43, 44}, which each may mediate K⁺ efflux following PAR1-induced [Ca²⁺]_i rises. To examine this possibility, we repeated the above PAR1-activation experiments in the combined presence of the selective inhibitors paxilline (Pax) and Tram-34 (T-34) that specifically block BK and IK channels, respectively. Again, arterioles lacking perivascular glioma cells did not alter their vessel diameter following PAR1 activation (n=17) (Fig. 7a). However, arterioles with perivascular glioma cells constricted significantly less (n=15) (Fig. 7a) in the presence of these K⁺ channel blockers suggesting that efflux of K⁺, from the glioma cells, contributed to glioma-mediated vasoregulation (one-tailed unpaired t-test with Welch correction, p=0.044, schematically depicted in Fig. 8). In cortical astrocytes, the concentration of K⁺ released determines whether vessels dilate or constrict³⁵. Therefore it is conceivable that glioma cells similarly are capable of causing either constrictions or dilation.

Figure 7. Perivascular glioma cells can hijack control over vasculature tone similar to astrocytes.

Average change in vessel diameters observed in high (h) (95%) oxygen for vessels associated (grey) and not associated (black) with glioma cells when exposed to 100 μM TFLLR or 100 μM TFLLR + 2 μM paxilline (Pax) + 2 μM Tram-34 (a). Changes in vessel diameter for an arteriole associated (grey) and not associated (black) with perivascular glioma cells over the course of one experiment when exposed to 100 μM TFLLR. Changes in Ca²⁺ (ΔF/F) in perivascular GCamp3-GFP-expressing glioma cells were simultaneously measured over the course of this experiment (b). DIC images of vessel associated with glioma cells ((-)Tumor Cells) before and after sufficient exposure to 100 μM TFLLR (left), ((+)Tumor Cells) before and at most constricted time point after application of 100 μM TFLLR (right), red lines indicate position of diameter measurement and vessel diameter before drug application, blue arrows indicate vessel diameter, Scale, 10 μm (c). Statistical data provided in results section, error bars refer to SEM. Acute slices from mice bearing GCamp3-GFP-expressing D54 gliomas that also expressed the red fluorescent protein tdTomato were loaded with DMNPE-4 caged Ca²⁺. [Ca²⁺]_i uncaging in TdTomato-positive glioma cells located at arterioles resulted in vascular responses (n=3), this example shows a dilation (d) Scale, 20 μm. Traces showing a fast [Ca²⁺]_I increase preceding the vascular response and slower oscillations at later time points. Data were corrected for dye bleaching using the bleach correction macro for ImageJ. (e).

Discussion

Using a clinically relevant mouse model of glioma, which replicates the salient features of the disease including diffuse perivascular invasion⁴⁵, peritumoral excitotoxicity^{46, 47}, and seizures⁴⁶, we investigated the interaction of invading glioma cells with host cerebral blood vessels during early stages of disease questioning whether invading, perivascular glioma cells may disrupt the astrocyte-vascular contact and in turn compromise their functional interactions. Using brain slices and in vivo imaging, we show that the vast majority of glioma associate with existing vessels and can displace the astrocytic endfeet from the vascular surface. This can cause a loss of endothelial cell TJs resulting in the extravasation of blood-borne molecules such as albumin, cadaverine, or cascade-blue tracers into the brain's parenchyma. Vessels occupied by gliomas no longer respond to astrocyte-released vasoregulators. Once vessels are fully encased, gliomas assume the regulation of vascular tone in part through the release of K⁺ via Ca²⁺-activated K⁺ channels.

Gliomas are known as highly vascular cancers and past studies have extensively studied glioma-mediated neovascularization and angiogenesis¹⁷. Glioma-released vascular endothelial growth factor (VEGF) incites microvascular proliferation and produce naïve, leaky, and dilated blood vessels⁴⁸. Tumor tissue from Glioblastoma patients show downregulation of key TJ proteins including claudin-1, -3, and -5^{6, 49}, which explains why tumors present with leaky BBBs as also observed in our mouse model.

In contrast to previous studies, we examined glioma-vascular interactions at a much earlier disease stage during a period termed vascular co-option, which precedes angiogenesis. Here, invading glioma cells, known to prefer the perivascular space for invasion²⁰, wrap themselves around the abluminal surface in a parasitic manner^{16, 18} often fully encasing blood vessels. Our data show that single invading cells or small groups of cells are sufficient to cause a local breach of the BBB. This could be attributed to the physical separation of the endfoot from the vessel surface. Such interdependence had been postulated⁵⁰, however a model examining selective astrocytic endfoot separation from the vasculature had not existed. Alternatively, contact and interaction of glioma cells with the vasculature could impair BBB functionality and expression of TJ proteins directly. A lack of pericytes is associated with BBB damage during development and in the aging brain⁵¹. Furthermore, activation of a proinflammatory cascade in pericytes in response to ApoE4 expression, leads to BBB breakdown⁵². For future studies, it will be interesting to examine whether pericytes contribute to BBB breakdown in response to glioma invasion. Irrespective of the cause, this finding is unexpected and exciting, because it suggests that small groups of invading tumor cells are not protected from the reach of chemotherapeutic drugs by the BBB as previously assumed, and aggressive chemotherapy could be considered at early stages of the disease when invasion is still rampant.

A second major finding of our study relates to the loss of functional coupling of astrocytes to regional blood flow. We find that the physical displacement of the astrocytic endfoot by gliomas prevents vasoactive molecules from reaching the vascular endothelial cell, while the VSMCs are largely unaffected by the presence of gliomas and still respond to vasoactive molecules directly applied (Summarized in Fig. 8). We stimulated astrocytic GPCRs using two drugs, trans-ACPD and NE, which have previously been shown to selectively induce [Ca²⁺]_i rises in astrocytes^{11, 34, 35} causing dilation in 20% oxygen and constriction in 95% oxygen. We complemented the pharmacological experiments by directly uncaging [Ca²⁺]_i in single astrocytes close to vessels. Indeed, vessels not occupied by gliomas showed identical responses to those previously published^{11, 34, 35} with either the pharmacological approach or photo-uncaging of Ca²⁺. Remarkably, we found a wide range of constrictions and dilations after Ca²⁺ uncaging. This is likely due to different levels of Ca²⁺ increases in the astrocytic endfeet as modest increases in Ca²⁺ induce dilation whereas larger increases cause constrictions⁹. In addition, the vascular response is dependent on [K⁺]_o levels. Raising extracellular [K⁺]_o switches dilation to constriction in brain slices. Indeed, we observed only constrictions when we applied high [K⁺]_o to slices independent of the oxygen tension.

Changes in blood flow are no longer regulated by astrocytes in areas of tumor invasion, which agrees with a reduction of blood flow in glioma patients⁵³. Moreover, as contact is lost, astrocytes can no longer transport energy metabolites such as lactate to supply them to neurons⁵⁴. The loss of adequate energy supply may hasten the excitotoxic neuronal demise. Interestingly, a number of other neurological diseases such as Alzheimer's disease^{55, 56}, hypertension⁵⁷, and diabetes⁵⁸ have also reported impaired NVC, likely contributing to the complicated pathological processes occurring in each of these diseases.

Finally, we show that vessel-associated glioma cells can actively regulate vessel tone. Our data suggests a significant vasoconstriction due to Ca²⁺-activated K⁺ channel-mediated K⁺ release, which we experimentally induced through activation of the PAR1 receptor, which is highly expressed in gliomas⁴¹. Given that Par1 expression has been reported in other CNS cell types⁵⁹, we complemented this approach by cell-type specific photo-uncaging of Ca²⁺ in glioma cells and confirmed a vascular response after artificial Ca²⁺ increase in glioma cells. We did not see any response when control vessels were stimulated, suggesting that under our experimental conditions TFLLR-induced PAR1 activation does not induce the release of vasoactive molecules from astrocytes or the endothelium. Of note, PAR1 receptor activation is likely to occur in human disease⁵⁹. The natural PAR1 ligands are blood-born thrombin or plasmin⁴², which can enter the brain through the focally breached BBB in areas where gliomas are present.

Vasoregulation by K⁺-release via Ca²⁺-activated K⁺ channels was first shown in cortical astrocytes and depending on [K⁺]_o, vasodilation or vasoconstriction can occur⁹. Glioma cells highly express Ca²⁺-activated K⁺ channels, including BK and IK channels. Early experiments showed that these channels facilitated invasion and migration⁴⁴, but our studies now suggest a mechanism by which glioma cells use these channels to flux K⁺ to modulate vessel diameter.

Glioma-mediated control over vessel diameter may be context specific supporting different aspects of glioma biology. More specifically, invading glioma cells may induce vasoconstriction in an attempt to increase the perivascular space needed to facilitate perivascular invasion. Growing satellite tumors, on the other hand, may benefit from dilated vessels shunting additional blood towards the tumor. In either situation, disrupting this tumor control over blood flow may impair tumor growth or invasion and should be exploited therapeutically in the future.

Methods

Animals

Mice were bred and maintained in a specific pathogen free barrier facility and all procedures were approved and performed in accordance with guidelines of the Institutional Animal Care and Use Committee (IACUC) of the University of Alabama at Birmingham.

Mice were housed in groups of 5 animals at maximum and subjected to a standard 12h light/12h dark cycle. Adult 8 to 12 weeks old C.B.17 scid mice of either sex were used for tumor implantations unless stated otherwise. Immunodeficiency is required to allow growth of tissues derived from a different species, which would otherwise be suppressed by the host's immune system.

Swiss Webster-Aldh1l1-eGFP bacterial artificial chromosome (BAC) transgenic mice (generated by the GENSAT project) were crossed to C.B.17 scid mice and genotyped for the scid^Prkdc point mutation as previously described ⁶⁰. Mice homozygous for the scid^Prkdc mutation and positive for GFP (Aldh1l1-eGFP-scid) were maintained as a colony and offspring of either sex was used for experiments.

Study design

The data contained in the manuscript are not prospective clinical or preclinical trials but instead controlled laboratory experiments pursuing a mechanistic analysis of biological processes in a mouse model of glioma. Hence we used descriptive statistics for all evaluations. Sample sizes were identical to those used in prior studies of other laboratories, and in each instance the appropriate reference was listed. Sample sizes were not altered during the study.

Surgical procedure

Human or mouse glioma cells were implanted into 6-12 week old immunodeficient C.B.-17 scid or Aldhl1l-eGFP-scid mice of either sex. On the day of surgery, once animals were anesthetized by 2-5% isoflurane, a midline scalp incision was created. A 0.5 mm burr hole was made at 1.0-2.0 mm and 0.5-1.0 mm posterior from bregma. Gl261-dsRed mouse glioma (1.0-1.5 × 10⁵), D54-EGFP human glioma cells (1.25-5.0 × 10⁵), patient-derived xenograft tumors (GMB14, GBM22 and GBM39; 1.0-1.5 × 10⁵) or non-malignant glia cells from Aldh1l1-eGFP-scid (0.25-1.0 × 10⁵) were injected into either one or both hemispheres at 1.0-2.0 mm depth (z axis at an angle of 35°). Following surgery, intracranial tumors grew for 2-4 weeks. Body weight was monitored periodically and mice showing significant loss of body weight indicating tumor growth were chosen for experiments.

Patient-derived xenograft tumor lines

Patient xenograft cells were derived from primary brain tumor tissue that was not specifically collected for this project (generous gift by Dr. Yancey Gillespie, Brain Tumor Tissue Core, University of Alabama at Birmingham, Birmingham, AL, USA) and maintained by serial passage in the flank of athymic nude mice, as previously described²². In short, tumors were harvested from the flanks after 2-3 weeks. The tissue was chopped into small pieces, waged in PBS and per mouse 200 μl of the solution was injected subcutaneously into the flanks of athymic nude mice to maintain the tumors. The remaining solution was dissociated using GentleMACS Tumor Dissociation Kit (MACS Miltenyl Biotec) and maintained in culture as spheres in Neurobasal-A medium (Invitrogen) supplemented with 10mg ml^-1 of EGF and FGF (Invitrogen), 250 μM ml^-1 amphotericin, 50mg ml^-1 gentamycin (Fisher), 260 mM L-glutamine (Invitrogen), and 10 ml B-27 supplement without Vitamin A (Invitrogen). Xenograft cells were maintained as spheres in vitro for 5-7 days before intracranial injections in scid mice.

Flank tumors and D54 cells were probed for their VEGF expression profile by Western blot analysis. D54, GBM14, and GBM39 do not show detectable VEGF protein levels, whereas VEGF expression is low in GBM1066 and higher in GBM12 and GBM22 (Supplementary Fig. 10).

Glioma preparations for implantation into scid mice

Most studies using tumor-bearing mice stereotactically implanted glioma cells derived from D54-MG (D54) glioma cells (WHO IV, glioblastoma multiforme; Dr. D. Bigner, Duke University, Durham, NC) confirmed to exhibit the salient features of the human disease⁴⁶. A stable cell line, D54-eGFP, was generated by transfecting D54-MG cells with pEGFP-N1 (Clonetech) and plasmid insertion was sustained with 0.10 mg ml^-1 G418 disulfate salt (Invitrogen). Gl261-dsRed cells were obtained from Frank Winkler (LMU, Munich, Germany). Cells were maintained in Dulbecco's modified Eagle's medium/F-12 (DMEM/F12) supplemented with 2 mM L-glutamine (Invitrogen) and 7% fetal bovine serum (FBS; Aleken Biologicals). Generation of lentiviral plasmids was performed in conjunction with the UAB Neuroscience NINDS Protein Core. To generate a red fluorescing D54 cell line the pLVX-IRES-tdTomato vector was used. To prepare the lentivirus, pLVK-IRES-tdTomato vectors together with helper plasmids (pPLP1, pPLP2 and pVSVg) were transfected into 293FT cells using Polyfect reagent (Qiagen) per the manufacturer's recommendations. 72 hours post-infection, virus-containing media was collected and stored at -80°C until utilization. To stably transduce lentiviral vectors into D54 glioma cells, virus-containing supernatant and 3 μg ml^-1 Polybrene was added to glioma cells plated 48 hours prior to transduction. 24 hours later, the virus-containing medium was exchanged for fresh media and allowed to proliferate for a minimum of 72 hours. Following this, a clonal population of TdTomato-expressing D54 cells was selected for the experiments. To generate D54-GCaMP3 cell line, pN1-GCaMP3 (Addgene) was cotransfected using the Cell Line Nucleofector™Kit T (Amaxa). D54 cells were plated 48 hours prior to transfection to achieve 70-80% confluency. On the day of transfection, the cells were harvested and 2 × 10⁶ cells were mixed with 3 μg of plasmid DNA in 100 μl of the transfection reagent and electroporated via the Amaxa Nucleofector (Amaxa) using program T-27. Following electroporation, cell suspension was transferred to 6-well cell culture plate (BD Biosciences) with 7% serum-containing media (DMEM/F12) and the media was exchanged the following day. A clonal population of D54-GCaMP3-GFP cells was selected for the experiments. For laser-uncaging of Ca²⁺ in glioma cells, a D54 clone was used that expressed TdTomato in addition to GCaMP3-GFP. All glioma cells were grown at 37°C and 90% O₂/10% CO₂ humidified environment.

Glial cell culture obtained from Aldh1l1-eGFP mice

The forebrain from 4-7 postnatal Aldh1l1-eGFP-scid mice (2–5 d old) was dissected and mechanically dissociated in Hanks' buffered saline solution containing 10 mM HEPES. After washing in DMEM medium supplemented with 10% fetal calf serum, 10 mM HEPES, and Penicillin/ Streptomycin, a single cell suspension was plated into 3 T75 flasks), and the medium was changed every other day. Glial cells were used for intracranial implantations after reaching confluence.

Drugs and solutions

All chemicals were obtained from Sigma Aldrich unless otherwise specified. 9,11-dideoxy-9α,11α-methanoepoxy prostaglandin F2α (U46619) and prostaglandin E₂ (PGE₂) were obtained from Cayman Chemical and diluted with DMSO, (±)-1-Aminocyclopentane-trans-1,3-dicarboxylic acid (trans-ACPD), paxilline and Tram-34 were obtained from Tocris Bioscience.

Immunohistochemistry

Tumor-implanted animals were perfused with phosphate buffered saline (PBS) followed by 4% paraformaldehyde (PFA) in PBS. 50-100 μm coronal slices were sectioned at the vibratome and blocked for 30 minutes in blocking solution (10% goat serum, 0.5% Triton-X in PBS) at room temperature. Any slices stained with antibodies raised in mice were incubated with goat anti-mouse F(ab′)₂ fragment affinity-purified antibody (Jackson Immunoresearch; 1:20) overnight at 4° C prior to the antibody staining. Slices were then washed in PBS and incubated in primary antibodies, diluted in the blocking solution, overnight at 4° C. Primary antibodies used included mouse Cy-3 alpha smooth muscle actin (Sigma Aldrich; Cat. # C6198; 1:2000), rabbit aquaporin-4 (Sigma Aldrich; Cat. # A5971; 1:400), mouse Human Nuclei (Millipore; Cat. # MAB1281 and MAB1281B; 1:100), and ratCD31 (BD Biosciences; Cat. # 550274; 1:150). Slices were again washed in PBS and stained with secondary antibodies for 1 hour at room temperature. Secondary antibodies used included goat anti-rat Alexa Fluor 647, goat anti-rabbit Cy3, goat anti-rabbit Alexa Fluor 647, and goat anti-mouse Cy3. For antibodies imaged using the 405 nm diode laser, the TSA™ Plus Coumarin System (Perkin-Elmer) was used per the manufacturer's instructions. Slices stained with rabbit zonula occluden-1 (ZO-1) (Invitrogen; Cat. # 402300) and rabbit claudin-5 (Novus Biologicals; Cat. # NB100-91713) underwent pepsin antigen retrieval (100 mg pepsin in 10 mM hydrochloric acid (HCl)) for 20 min at 37°C. Slices were then washed twice with PBST (PBS with 150μl l^-1 Tween-20), incubated in 3% H₂O₂ for 10 minute, and then washed three times with PBS before incubating with primary antibody overnight for a minimum of 48 hours at 4°C. Slices stained with Alexa Fluor 633 hydrazide dye (Invitrogen) were incubated in a 20 μM solution of the dye diluted in PBS for 2 min. Slices were washed with PBS and mounted on glass slides with AquaPolymount (Polysciences). Images were acquired using the Olympus Fluoview FV1000 laser scanning microscope (Olympus) equipped with 4 diode lasers (405, 473, 559, 635 nm) using a UPLFLN-40X air objective (Olympus). Experiments were successfully repeated; limitations in repeatability of immunohistochemistry or the described results were not encountered. However, tumor sizes and number of migrating tumor cells were variable.

Quantification of vessel areas covered by zona occludens-1 positive tight junctions was done using Fiji/Image J. Confocal images of areas with vessels co-opted by D54 glioma cells and neighboring areas free of tumor were taken. Binary images of 5 μm stacks were created and the area of CD31 positive vessels and ZO1 was determined. For vessels coopted by glioma cells, only the vessel area covered by glioma cells was taken into account. To account for variability in the staining from animal to animal, values from glioma images were directly compared to the values of the glioma-free neighboring region in the same brain section.

Western blot

Tumor tissue was was lysed in RIPA buffer and homogenized using a dounce tissue grinder (Wheaton). After sonication, homogenates were centrifuged for 5 min at 12,000 × g at 4°C. Protein quantification was performed on the supernatant using a BCA protein assay kit (Thermo Scientific). Laemmli-SDS sample buffer, containing 600 mM b-Mercaptoethanol, was added to the protein samples before incubating them at 95°C for 10 min. 15 μg of protein were loaded into each lane of a 4-15% gradient precast acrylamide SDS-PAGE gel (Biorad). Samples were separated at 100-200 V. Protein was transferred onto 0.45 μm PVDF Transfer membranes (Thermo Scientific, #88518) in Mini Trans-Blot® Electrophoretic Transfer Cells (Biorad) at 100 V for 1 hr. Membranes were blocked in Tris buffered saline with Tween (TBST) (0.1 % Tween 20 in TBS) containing 10 % non-fat dried milk for 30 min at room temperature or at 4°C overnight. Blots were incubated in primary antibody solution (mouse anti-VEGF, Sigma V4758, 2ug ml^-1) (TBST, 10 % goat serum and antibody) at 4°C overnight. Blots were washed in TBST 3 × for 10 min and incubated in secondary anti-rabbit, anti-mouse or anti-sheep horseradish peroxidase-conjugated antibody 1:1500 (Santa Cruz) for 1 hr at room temperature. Membranes were washed in TBST 3 × for 10 min and developed using a luminol (Santa Cruz) chemiluminescence kit, and chemiluminescence was detected using a 4000 MM Kodak imaging station and Kodak molecular imaging software v.4.0.4.

In vivo 2-photon imaging through a cranial window

Animals were anesthetized with 2-5% isoflurane. The hair and skin of the skull was removed. A metal bar was secured to the skull behind lambda by dental cement. Removal of the skull anterior to lambda and posterior to bregma was performed on one hemisphere. Animals were injected into the tail vein with 200 μL of 5 mg ml^-1 70,000 MW tetramethylrhodamine dextran (Invitrogen) with a 28 gauge, 0.5 inch long needle (BD Biosciences). Animals were placed on a custom built apparatus with a heating pad and the metal bar was secured to immobilize the animal's skull. Arteries and arterioles were identified by their size (<7 μm) and direction of blood flow or by retro-orbitally administered Alexa Fluor 633 Hydrazide (Invitrogen). Using a multiphoton laser scanning fluorescence microscope (Prairie Technologies) equipped with a X40/0.8 N.A. W water-immersion objective (Olympus) Z stacks of perivascular glioma cells were acquired. Channels were unmixed using ImageJ software and projection images created using Imaris x64 7.5.2 Software (Bitplane Scientific Software).

Electron microscopy

Tumor-implanted animals were perfused with PBS followed by a fixation solution of 2.5% glutaraldehyde, 4% PFA in 0.1 M Sodium Cacodylate (Caco) buffer, pH 7.4. After fixation, the brain was removed and sectioned into 100 - 500 μM slices. Under a fluorescent dissection microscope, tissue punches were taken to capture tumor and non-tumor areas. Punches were placed in fixation solution overnight at 4°C. Samples were washed 2 times for 15 min in 0.1M Caco buffer, pH 7.4 and then immersed in 1% osmium diluted in 0.1M Caco buffer, pH 7.4 for 50 min at room temperature on a rotator in the dark. Samples were then washed 4 times in 0.2M Caco buffer, pH 7.4. Samples were dehydrated in 50% 80% and 95% acetone for 5 min each. 4 washes in 100% acetone for 15 min were performed. Samples were equilibrated for embedding in a solution containing equal parts of 100% acetone and Epon 812 with accelerator on a rotator overnight at room temperature. Samples were embedded in 100% Epon 812 with the accelerator at 60-70°C overnight. Ultrathin sections were cut and imaged on a Tecnai T12 120kV Transmission Electron Microscope (FEI).

Blood-brain barrier permeability assays

Tumor-implanted animals were injected with 200 μL of the tracers via tail vein. These tracers were allowed to circulate for 2-3 hours before animals were deeply anesthetized and perfused with PBS followed by 4% PFA. Concentration of used tracers was as follows: 2% Evan's blue (Sigma) in saline, 1mg ml^-1 bovine serum albumin conjugated to Alexa Fluor-555 (Invitrogen) in saline, and 500 μg/animal lysine-fixable cadaverine conjugated to Alexa Fluor-555 (Invitrogen) in saline. After adequate fixation, 50-100 μm coronal slices were cut and immunohistochemistry was performed as described above. For the in vivo tracer injection experiments, 100 μL of 12.5 mg ml^-1 10,000 MW Cascade Blue (Invitrogen) and Alexa Fluor 633 hydrazide dye (0.2 mg ml^-1) was retro-orbitally injected. These animals were anesthetized with 2-5% isoflurane and placed on a custom built apparatus with a heating pad and the metal bar was secured to immobilize the animal's skull. Images were acquired using a 4 detector Olympus FV-1000MPE multiphoton laser scanning microscope with a Coherent Chameleon Vision II Ti:Sapphire laser (Olympus) with a XLPN 25X/1.05 N.A. water immersion objective to visualize 4 different dyes. Channels were unmixed using Olympus Fluoview Software Version 3.1b. Projection images were created using ImageJ software.

Acute brain slice drug application experiments

Animals were sacrificed and brains were placed in ice-cold artificial cerebrospinal fluid (cutting ACSF) bath solution (135 mM N-methyl-D-glucamine, 1.5 mM KCl, 3.5 mM MgSO₄, 0.5 mM CaCl₂, 1.5 mM KH₂PO₄, 23 mM choline bicarbonate, 25 mM D-glucose and 0.4 mM ascorbic acid bubbled with 95% O₂/5% CO₂ to maintain pH at 7.4). 200 μm coronal slices were sectioned and allowed to recover for 45 min to 1 hour at 28°C in recording ACSF (125 mM NaCl, 3.0 mM KCl, 1.25 mM NaH₂PO₄, 25 mM NaHCO₃, 25 mM D-glucose, 2.0 mM CaCl₂, 2.0 mM MgSO₄) bubbled with 95% O₂/5% CO₂ to maintain pH at 7.4. When specified, vessels were preconstricted in 125 nM U46619 for 20 min in recording ACSF bubbled with 95% O₂/5% CO₂ at 37°C. For experiments at “low oxygen” concentrations, slices were transferred to recording ACSF bubbled with 20% O₂/5% CO₂ for a minimum of 20 minutes before the onset of the experiment. Acute brain slices were transferred to a Leica DM LFSA upright DIC-IR fluorescence microscope using a Zeiss Hm digital camera at 1000× magnification (Leica Microscopy). Slices were continually perfused with recording ACSF heated to 33° C and bubbled with “high oxygen” conditions (95% O₂/5% CO₂) or “low oxygen” conditions (20% O₂/5% CO₂). Timelapse images of vessels were acquired using Axiovision 4.7 software (Carl Zeiss Microscopy). Vessel diameter was measured as the cross-section of the vessel using ImagePro (Media Cybernetics) or ImageJ software (NIH Image, NIH).

Acute brain slice calcium uncaging experiments

After obtaining slices as described above slices were allowed to recover for 1hr in ACSF bubbled with 95% O2/5% CO2 at room temperature to maintain pH at 7.4). Slices were loaded with 40 μM Alexa Fluor 633 Hydrazide (Invitrogen), 10 μM Fluo-4 acetoxymethyl ester AM (Invitrogen) Ca²⁺ indicator, and 10 μM DMNPE-4 caged Ca²⁺³⁶ in ACSF containing 0.02% pluronic acid for 60 min at room temperature. Slices were then transferred to regular ACSF to allow for stabilization before recording. Alexa Fluor 633 Hydrazide and Fluo-4 AM fluorescence was detected by laser scanning confocal microscopy using an Olympus FV1000 and a 60×/1.1 NA water immersion objective (Olympus). Single plane confocal images of 800 × 800 or 640 × 640 pixels were obtained every ∼2 s. Ca²⁺ uncaging was achieved using a 405 nM laser in ROI tornado scanning mode at 40% power for 800 ms that was directed at astrocytic end feet associated with arterioles identified by Alexa Fluor 633 Hydrazide dye. Vessel diameter was measured as the cross-section of the vessel using ImageJ software (NIH Image, NIH).

Statistical Analysis

All data obtained was analyzed using Origin 6.0 software (Microcal Software). Statistical tests were performed using GraphPad Instat (GraphPad Software Inc,) or GraphPad Prism 6.0; specific tests are stated in the results. All measurements are reported with standard error of mean. The KS normality test was performed for each data group. If normality was not achieved, a Mann-Whitney test was performed instead of the unpaired t-test. The specific test is stated in the results and figure legends. No data/outliers were excluded from the analysis. The number of replicates is reported in the results and figure legends.