Contribution of cell death signaling to blood vessel formation

Abstract

The formation of new blood vessels is driven by proliferation of endothelial cells (ECs), elongation of maturing vessel sprouts and ultimately vessel remodeling to create a hierarchically structured vascular system. Vessel regression is an essential process to remove redundant vessel branches in order to adapt the final vessel density to the demands of the surrounding tissue. How exactly vessel regression occurs and whether and to which extent cell death contributes to this process has been in the focus of several studies within the last decade. On top, recent findings challenge our simplistic view of the cell death signaling machinery as a sole executer of cellular demise, as emerging evidences suggest that some of the classic cell death regulators even promote blood vessel formation. This review summarizes our current knowledge on the role of the cell death signaling machinery with a focus on the apoptosis and necroptosis signaling pathways during blood vessel formation in development and pathology.

Introduction

Blood vessels are lumenized structures with an inner lining of a single layer of endothelial cells (ECs) that transport oxygen and nutrients throughout the body. After the de-novo formation of an initial primitive vascular system by accumulation of angioblasts and blood islands (vasculogenesis), the vascular system develops by sprouting of new vessels from already pre-existing ones (angiogenesis) [1]. Angiogenesis is followed by EC differentiation into arteries, veins and capillaries and ultimately vessel remodeling to acquire a hierarchically structured vascular system. The diversity of these processes indicates that factors regulating EC survival must be balanced to allow resistance to exogenous stresses during organ growth, while promoting vessel pruning (removal of single vessel segments during the process of vascular optimization) or regression (defined here as elimination of multiple vessel segments as part of a mechanism of vascular rarefaction) and thus maturation of the vascular system. Even though the adult vascular system is very stable, with a low turnover of ECs during homeostatic conditions, the endothelium maintains its plastic capacity. For example, the vasculature readily adapts to the metabolic demands of its surrounding tissue by either reducing or increasing vessel density, such as in physiological conditions like the regression of the corpus luteum during the female reproductive cycle [2], exercise [3, 4] or wound healing [5], or in pathological conditions like malignant tumor growth [6].

Whereas it is undoubted that EC death contributes to the complete removal of certain vascular networks during development, such as the hyaloid vasculature of the fetal retina [7–9] or the first, second and fifth aortic arches [10, 11] during the formation of the cardiovascular system, it seems that cell death is not a key driver for later stages of vessel pruning, when vessel branches only partially regress to improve the functionality of an existing vascular network [12]. Recent evidences suggest that under such conditions, the activity of the cell death signaling machinery can even promote angiogenesis and blood vessel development [13–15].

In addition to these physiological examples, excessive EC death can also lead to pathological vessel regression, such as it occurs during retinopathy of prematurity (ROP), when preterm infants are exposed to high oxygen levels. Vice versa, impaired EC death can cause persistent hyperplastic primary vitreous, a developmental human eye disease caused by defective hyaloid vessel regression [16, 17]. On the other hand, targeting the cell death signaling machinery in ECs to inhibit blood vessel formation and vascularization during cancer development, thus promoting tumor regression, could be used as a valuable therapeutical strategy [18].

We start this review with a brief introduction into the different cell death signaling pathways regulating apoptosis and necroptosis (Fig. 1) and discuss how these are required to promote full regression of specific vascular systems, using the hyaloid vasculature of the fetal retina as an example. We will then summarize our current knowledge about vessel remodeling at later developmental stages and highlight the cell death independent functions of the cell death signaling machinery to this process. Finally, we will discuss the pathological contributions of EC death to vascular diseases, and its benefits in anti-angiogenic cancer therapy.

Fig. 1.

Simplified schematic overview of the BCL2-regulated and death receptor-mediated apoptosis and necroptosis signaling pathways. In the BCL2 pathway, interactions between pro- and anti-apoptotic BCL2 sub-family members determine whether the pro-apoptotic effectors BAK and BAX become activated. This results in increased mitochondrial permeability and cytochrome C (Cyt C) release, which, in turn, favors the formation of the death inducing apoptosome and ultimately Caspase-3 (CASP-3) cleavage by the initiator Caspase-9 (CASP-9). In the extrinsic pathway, binding of a death ligand to its death receptor leads to formation of the death inducing signaling complex (DISC) and activation of the initiator Caspase-8 (CASP-8). In the DISC, CASP-8 activity is restricted when CASP-8 binds to its inhibitor c-FLIP. Full CASP-8 activity in the absence of c-FLIP leads to CASP-3 cleavage, activation, and cell death by apoptosis. On the other hand, a minimal CASP-8 activity within the DISC is required to inhibit cell death via necroptosis. Loss of CASP-8 or inhibition of its enzymatic activity result in the formation of the necrosome including RIPK3, and ultimately activation and phosphorylation of the necroptosis executer MLKL. For reasons of simplicity, only key molecules of the different signaling complexes are highlighted. For further reading, we kindly refer the reader to reference [19]

Molecular regulation of apoptosis and necroptosis

Two separated, but converging, pathways control apoptosis (Fig. 1): one is the so-called intrinsic, mitochondria dependent pathway regulated by the BCL2 family of proteins and the other one is regulated via extrinsic factors that activate the death receptor induced cell death signaling pathway. Both pathways result in the activation of initiator Caspases such as Caspase-8 (CASP-8) and -9 that in turn cleave and activate downstream Caspases (e.g. CASP-3 and -7) to implement the cell death program [19].

Intrinsic cell death signaling pathway

Proteins of the BCL2 family share the presence of short segments of sequence homology referred to as the BCL2 homology (BH) regions and are divided into three sub-families that can have pro- or anti-apoptotic properties [20]. BCL2 has been the first identified member of the pro-survival sub-family, which also includes BCLxL, MCL1, and others [20, 21]. The other two sub-families are pro-apoptotic. The BH3-only sub-family (e.g. BIM, BID, BAD, PUMA), so-named because its members only share the BH3-region [22], are regulated by apoptotic stimuli and initiate apoptosis via BAX and BAK, members of the other pro-apoptotic sub-family [23]. Upon oligomerization, BAX and BAK are responsible for mitochondrial outer membrane permeabilization (MOMP) [24, 25]. Interactions between the three BCL2 sub-families determine whether BAX and BAK become activated, as pro-survival BCL2 family proteins can either prevent BH3-only proteins from binding and thus activating BAX and BAK [26] or directly bind to the activated forms of BAX and BAK [27]. Recently, BOX was identified as a non-canonical pro-apoptotic BCL2 family member [28]. Whereas 10% of BAK/BAX double knockout mice survive to adulthood, with only minor developmental defects, the phenotype of BOX/BAK/BAX triple knockout mice is much more severe, with less than 2% of the mice surviving to adulthood [29]. While these findings demonstrate a certain redundancy amongst the pro-apoptotic BCL2 family members, it also shows that life in the absence of intrinsic apoptosis is possible.

During cell death, MOMP induces the release of Cytochrome C (Cyt C) [25] and other pro-apoptotic molecules. In turn, Cyt C in the cytoplasm favors the formation of the so-called ‘apoptosome’, a signaling platform that recruits and activates the initiator CASP-9 [30] which will then further cleave and activate the executioner CASP-3. Executioner Caspases have the ability to cleave diverse cellular substrates, such as lamin-β1 [31], β-actin [32] and poly (ADP-ribose) polymerase [33] and thus to induce the regulated cellular degradation during apoptosis. Not only growth factor deprivation, but also other intracellular risk factors such as DNA damage, hypoxia, or metabolic stress can activate cell death via the mitochondria-mediated intrinsic apoptosis pathway [34–36].

Extrinsic cell death signaling pathway and necroptosis

The extrinsic cell death signaling pathway is exogenously induced at a cell’s plasma membrane when a death ligand binds to its respective death receptor. Eight members of the death receptor family have been described so far, with the tumor necrosis factor (TNF) receptor superfamily, including TNFR1, TRAILR2 and CD95, being the most important ones [37]. All of them are type 1 transmembrane receptors that can be distinguished by a ~ 80 amino acids comprising cytoplasmic domain, known as the death domain (DD). Signal transduction of death receptors takes place in three general steps: 1) Binding of the death ligand to its receptor; 2) recruitment of adaptor proteins and the initiator CASP-8 (in humans CASP-10 is also recruited) to the DD, resulting in the formation of the death inducing signaling complex (DISC); 3) specific downstream signaling events depending on the stoichiometry of adaptor proteins and initiator caspases. Large amounts of activated initiator caspases can directly process and activate the executioner CASP-3, CASP-6 or CASP-7 [38]. However, in the presence of caspase inhibitory molecules of the inhibitor of apoptosis (IAP) protein family, or if smaller amounts of activated CASP-8 are available, efficient apoptosis depends on cleavage of the BH3-only protein BID by CASP-8. Truncated BID (tBID) can then translocate to the mitochondria to induce oligomerization of BAK and BAX to amplify cell death via the intrinsic pathway [38, 39].

CASP-8 activity is normally restricted and inhibited by heterodimerization with c-FLIP, a homologous protein that lacks catalytic activity [40]. Even though c-FLIP prevents the full activation of CASP-8, a restricted enzymatic activity of CASP-8 within the c-FLIP/CASP-8 heterodimer is necessary to prevent an alternative cell death pathway called necroptosis [41]. Necroptosis is induced upon autophosphorylation and activation of the receptor interacting protein kinases (RIPK) 1 and 3 [42, 43]. CASP-8 can directly cleave RIPK1 and RIPK3 [44, 45] and, therefore, prevent their kinase activity. In addition, CASP-8 indirectly inhibits RIPK1 by cleaving the deubiquitinase cylindromatosis (CYLD), as ubiquitinated RIPK1 cannot be recruited to the cytosolic death signaling complex anymore [46]. Mixed lineage kinase domain like protein (MLKL) is a target of RIPK1 and RIPK3 and the key executor of necroptosis [47, 48]. Phosphorylation of MLKL by RIPK3 induces a conformational change that promotes MLKL oligomerization and translocation to the plasma membrane. It is hypothesized that tetrameric MLKL can integrate into the plasma membrane, induce pore formation and thus cause the classical cellular rupture seen in necrotic cells [49, 50].

Regulation of cell death during development of the embryonic vascular system

Formation of the cardiovascular system starts around embryonic day (E)8 in mice [51]. Soon after the formation of the heart rudiments and looping and formation of the heart chambers, intraembryonic blood vessels start to form independently by accumulation of angioblasts that will later on connect to the heart circulation [52]. Whereas it is well described that some of the primordial pharyngeal arch arteries are removed by apoptosis  in the developing mammalian heart [53], only little is known about the contribution of cell death in ECs of the developing embryonic microvasculature.

Studies using genetic mouse models (Table 1) suggest that the embryonic vasculature is highly sensitive to EC death. Increased EC apoptosis often goes in hand with hemorrhage formation, defects in yolk sac vascularization and embryonic lethality. TAK1 is a kinase induced downstream of the TNFR1, where it activates Nf-κB signaling upon TNF-α stimulation [54]. EC-specific deletion of Tak1 leads to increased TNF-dependent EC apoptosis, reduced embryo angiogenesis, defects in yolk sac vascularization and ultimately embryonic lethality around E10.5 [55]. Other molecules of the extrinsic cell death pathway have also been implicated in regulating EC survival during embryonic development. For example, cFlip, Casp8, and Fadd knockout mice die during early embryonic development between E10.5–12.5 due to cardiovascular failure and compromised yolk sac vascularization [56–58]. These defects are rescued when either apoptosis or necroptosis are inhibited, as shown in double or triple knockout mice like c-FLIP^ko/FADD^ko/RIPK3^ko [59], Casp8^ko/RIPK3^ko [60] or Casp8/MLKL^ko [61] mice. In particular, EC-specific deletion of Casp8 [13, 62], FADD [63] and other pro-survival molecules [55, 64] of the extrinsic cell death signaling pathway recapitulates the severity of the full knockout of these genes, indicating that pro-survival molecules of the extrinsic cell death signaling pathway are required to promote EC survival during embryonic development. Additionally, a pro-survival role for the heterodimer of CASP-8 and c-FLIP was described in multiple other tissues in vivo [59].

Table 1.

Overview of the mouse mutants discussed in this review

Mouse line		Vascular phenotype			Reference
Name	Description	Embryonic development	Postnatal angiogenesis	Pathology
c-FLIP-/-	Ubiquitous knockout of the anti-apoptotic c-FLIP	Impaired cardiovascular development, embryonic lethality at ~ E10.5, defective yolk sac vascularization	n.d.	n.d.	Yeh et al. (2000)
Casp8-/-	Ubiquitous knockout of the initiator CASP-8	Impaired cardiovascular development, embryonic lethality a ~ E10.5, defective yolk sac vascularization	n.d.	n.d.	Varfolomeev et al. (1998)
Casp-8ECko	Endothelial cell specific knockout of the initiator CASP-8	Hemorrhages, embryonic lethality at E13.5, defective yolk sac vascularization	Impaired retina angiogenesis	OIR model: Increased vaso-obliteration, reduced tuft formation. B16 melanoma metastasis model: Increased metastatic spread	Kang et al. (2004); Tisch et al. (2019); Strilic et al. (2016)
FADD-/-	Ubiquitous knockout of the adaptor protein FADD	Impaired cardiovascular development, embryonic lethality at ~ E10.5, defective yolk sac vascularization	n.d.	n.d.	Yeh et al. (1998)
FADDECko	Endothelial cell specific knockout of the adaptor protein FADD	Impaired cardiovascular development, embryonic lethality at E11.5	n.d.	n.d.	Fan et al. (2016)
BAX-/-/BAK-/-	Ubiquitous knockout of the proapoptotic BCl2 members BAX and BAK	Improper formation of the aortic arches (phenotype not 100% penetrant)	Reduced hyaloid vessel regression	n.d.	Ke et al. (2018); Hahn et al. (2005)
BOX-/-/BAX-/-/BAK-/-	Ubiquitous knockout of the proapoptotic BCl2 members BOX, BAX and BAK	Less than 2% of the triple knockouts survive into adulthood	n.d.	n.d.	Ke et al. (2018)
PU.1-/-	Mouse model lacking macrophages	Reduced vascular anastomosis and vascular complexity in the embryonic hindbrain	Reduced hyaloid vessel regression	n.d.	Fantin et al. (2010); Lobov et al. (2005)
BIM-/-	Ubiquitous knockout of the proapoptotic BCL2 member BIM	n.d.	Reduced hyaloid vessel regression	Protection from hyperoxia induced vaso-obliteration	Wang et al. (2011); König et al. (2014)
BIMPC	Pericyte specific knockout of the proapoptotic BCL2 member BIM	n.d.	Increased pericyte and EC numbers, decreased apoptosis and proliferation of vascular associated cells, reduced hyaloid vessel regression, enhanced vertical sprouting into the deep vascular plexus	No protection from hyperoxia induced vaso-obliteration	Wang et al. (2017)
BIMEC	Endothelial cell specific knockout of the proapoptotic BCL2 member BIM	n.d.	Increased EC numbers, decreased apoptosis and proliferation of vascular associated cells, reduced hyaloid vessel regression, enhanced vertical sprouting into the deep vascular plexus	No protection from hyperoxia induced vaso-obliteration	Wang et al. (2017)
BIK-/-	Ubiquitous knockout of the proapoptotic BCL2 member BIK	No reported vascular abnormalities	Normal hyaloid vessel regression	n.d.	Coultas et al. (2004)
Endosialin-/-	Ubiquitous knockout of the type I transmembrane glycoprotein Endosialin which is expressed by pericytes	n.d.	Increased vessel density, reduced vessel regression	B16-xenograft: Reduced vessel remodeling in the primary tumor	Simonavicious et al. (2012)
Tie-1ECko	Endothelial cell specific knockout of theTIE1 receptor	n.d.	Increased EC death, reduced vessel density in the retina	B16-xenograft: Reduced tumor angiogenesis, increased tumor EC apoptosis	Savant et al. (2015)
EviECko	Endothelial cell specific knockout of the wnt secretion factor Evi	n.d.	Increased EC death, reduced vessel density in the retina, reduced EC proliferation, downregulation of survival genes	LLC model: reduced tumor vessel density	Korn et al. (2014)
RSPO3ECko	Endothelial cell specific knockout of the wnt signaling enhancer R-spondin-3	Embryonic lethality between E10.5–E13.5, defective yolk sac vascularization	Reduced retina vessel density, increased EC apoptosis	LLC model: reduced tumor vessel density, increased vessel regression	Scholz et al. (2016)
Mcl1ECko	Endothelial cell specific knockout of the anti-apoptotic BCL2 member Mcl1	Edema, hemorrhages, abnormal angiogenesis in the dorsal skin, embryonic lethality at E14.5	Reduced retina vessel density, increased EC apoptosis in proliferative areas, no defect in vessel regression	n.d.	Watson et al. (2016)
BAX-/- BAKEC/EC	Ubiquitous knockout of the proapoptotic BCL2 member BAX combined with the endothelial cell specific knockout of BAK	n.d.	Reduced hyaloid vessel regression, reduced retina EC apoptosis, but no difference in vessel regression and vessel density; increased capillary EC density	OIR model: No EC apoptosis during vaso-obliteration phase. However, vessel regression still occurs. Increased revascularization upon return to normoxia	Watson et al. (2016); Grant et al. (2020)
TAK1ECko	Endothelial cell specific knockout of the prosurvival protein TAK1	Embryonic lethalty at E10.5–E11.5, reduced angiogenesis, disorganized vasculature, defective yolk sac vascu-larization, increased TNF dependent EC apoptosis	n.d.	EL4 lymphoma and LLC model: Reduced tumor vessel density, increased tumor vessel permeability	Morioka et al. (2012); Naito et al. (2019)
SurvivinECko	Endothelial cell specific knockout of the IAP protein survivin	Diffuse hemorrhages, abnormal heart development, increased EC apoptosis, embryonic lethality at E13.5, defective yolk sac vascularization	n.d.	n.d.	Zwerts et al. (2007)
PUMA-/-	Ubiquitous knockout of the proapoptotic BCL2 member PUMA	n.d.	Reduced vessel density and EC number retina and brain. No difference in apoptosis	CNV: Reduced choroidal neovascularization	Zhang et al. (2012)
CD95ECko	Endothelial cell specific knockout of the death receptor CD95	n.d.	Reduced vessel density in the retina and brain, reduced EC proliferation, no difference in vessel regression	n.d.	Chen et al. (2017)
TRAIL-/-	Ubiquitous knockout of the death ligand TRAIL	n.d.	Increased vessel density in the retina at P3, but not P5 and later; small but significant decrease in the capillary free area surrounding the arteries	OIR: No difference in vaso-obliteration; increased number and delayed regression of neovascular tufts due to decreased EC apoptosis	Hubert et al. (2009)
Faslgld/gld	Loss of function mutation of the death ligand FasL (CD95L)	n.d.	n.d.	OIR: No difference in vaso-obliteration, increased formation of neovascular tufts,  reduced EC apoptosis	Barreiro et al. (2003); Davies et al. (2003)
Bcl-2-/-	Ubiquitous knockout of the anti-apoptotic BCL2 member Bcl2	No reported vascular abnormalities	No difference in hyaloid vessel regression, decreased vessel density, decreased EC and PC numbers, increased apoptosis in retinal vessels	No protection from hyperoxia induced vaso-obliteration, reduced tuft formation	Wang et al. (2005)
Bcl-2ECko	Endothelial cell specific knockout of the anti-apoptotic BCL2 member Bcl2	n.d.	Reduced EC numbers at P21 and P42, decreased retinal artery and vein number, no difference in vessel outgrowth, increased apoptosis and proliferation at P14	OIR: Increased vaso-obliteration, no difference in pathological tuft formation. CNV: Reduced neovascularization	Zaitoun et al. (2015)

n.d. (not determined) vasculature at a specific developmental stage or pathology has not been examined in detail

Interestingly, Tnfr1, TRAILR2 and CD95 knockout mice are viable and develop without obvious impairments [65–67], suggesting that death receptor signaling (the extrinsic cell death signaling pathway) in ECs is not essential for the proper formation of the embryonic vascular system. Nevertheless, it is possible that these mice still present transient vascular defects that are compensated during development and therefore do not result in a permanent vascular defect. For example, vessel density and complexity are attenuated in EC-specific CD95 knockout embryos [14].

Whereas the deathly potential of the extrinsic cell death signaling pathway in ECs during embryonic development has been substantially studied, the role of the intrinsic pathway has been less clearly defined. Due to the redundancy and large functional overlap of BCL2 family members, the developmental contribution of mitochondria-mediated cell death in the formation of the embryonic vascular system is difficult to elucidate. EC l-specific Mcl1 knockout embryos present abnormal angiogenesis in the skin and die at E14.5 due to edema and hemorrhages [68]. Whereas mice lacking BAX or BAK only display mild developmental defects that result in lymphoid cell hyperplasia and increased platelet numbers in the adult [69, 70], more than 90% of Bax/Bak double knockout mice die perinatally due to multiple reasons, including improper formation of the aortic arches [29]. Interestingly, the cardiovascular system in the survivors seemed largely normal, even though they presented multiple defects related to insufficient apoptosis in other tissues [29, 71]. This result indicates that cell death via the intrinsic pathway is either not essential in embryonic ECs or can be compensated and executed by BAX/BAK-independent mechanisms.

Taken together, the above-mentioned studies so far suggest that EC death is dispensable for proper formation of the early embryonic cardiovascular system, but has to be actively inhibited to allow embryonic development. It might be that a lack of apoptosis can be compensated by other cell death modalities. Therefore, it remains to be elucidated, whether combined inhibition of multiple cell death pathways would also be tolerated in the developing vasculature.

EC apoptosis during postnatal development

Regression of the hyaloid vasculature is mediated by the BCL2 signaling pathway

The hyaloid vasculature and pupillary membrane are specialized vascular structures in the eye of the embryo that supply trophic support to the growing lens during embryogenesis. In parallel to the development of the postnatal retinal vascular system (see below), both the hyaloid vessels and pupillary membrane regress [72]. Persistent fetal vasculature (PFV), one of the most common developmental congenital ocular malformations, is a human disease that results from inefficient removal of the hyaloid vasculature [73]. Interestingly, hyaloid vessel, but not pupillary membrane regression, is inhibited in Bax/Bax double knockout mice, where these vessels are still present in adulthood [17]. These results indicate that apoptosis in ECs is required for hyaloid vessel regression during development.

Pupillary membrane, and likely hyaloid vessel regression as well, takes place in two phases. In the first phase, macrophages induce apoptosis in single ECs, for example via Wnt-7b signaling [74–76]. This is followed by subsequent lumen constriction and thus disturbances in blood flow that induce a second phase of EC apoptosis in larger vessel segments [77, 78]. PU.1 mutant mice that lack resident macrophages [75] suffer from PFV , thus supporting a role of macrophages in the removal of these fetal vascular beds [9, 72, 74, 78]. Hyaloid vessel regression is also regulated by retinal neurons that express VEGFR2 and can titrate VEGF availability [8]. In this context, the BH3 only protein BIM is an essential inducer of apoptosis in ECs and normally suppressed by VEGF signaling [79, 80]. Therefore, hyaloid vessel regression is inhibited in Bim^−/− mice [80, 81]. In contrast, loss of the pro-apoptotic BH3 only protein BIK [82] or the antiapoptotic BCL2  [83] did not affect hyaloid vessel regression, indicating again redundancy of some of the BH3 family members.

Apoptosis during angiogenesis in the mouse retina

The retina vasculature develops in utero in humans [73]. However, in mice, this vasculature develops postnatally during the first 3 weeks after birth [84]. Much of our knowledge of the different phases of angiogenesis (sprouting and growth, maturation and remodeling) has come from studying the neonatal mouse retina [85, 86], and different genetic mouse mutants have been analyzed to understand the contribution of cell death to these processes (Table 1). Starting at postnatal day (P) 1, vessel sprouts emerge from the optic nerve head at the center of the retina from where they expand radially towards the retina periphery until ~ P8 [85]. Whereas EC proliferation and vessel sprouting mainly take place at the leading edge of the growing vascular system, vessel maturation predominantly occurs more centrally. Nevertheless, this division is not absolute as EC proliferation is also observed in and around the central vein segments [87], and pruning vessels can be found throughout the vessel network [88]. A small subset of apoptotic ECs has been observed during retina angiogenesis [12, 88–90]. While these few apoptotic ECs are initially clustered around remodeling arteries, away from proliferative regions of the retina, they appear more evenly distributed over time as soon as EC proliferation ceases [12].

Maturing vessels become covered by mural cells that provide pro-survival factors such as ANG-1 [91] and VEGF [92]  to promote EC survival, vessel stability and integrity. In line, EC apoptosis during retina angiogenesis increased dramatically in the absence of pericytes [93]. In these conditions, the remaining vasculature presented defective blood–retinal barrier formation and vascular hemorrhages due to the upregulation of vascular destabilization factors in ECs, such as ANG-2, downstream of FOXO1 [93]. Consistently, EC apoptosis is decreased in pericyte-specific Bim knockout mice (where pericyte numbers are increased [94]), indicating that pericytes are crucial for EC survival during vessel growth. On the other hand, one study reported that pericytes promote EC apoptosis in the postnatal retina through the production of endosialin, whose expression is restricted to pericytes covering newly formed vessels [95]. Whether pericytes undergo cell death during physiological blood vessel pruning is also controversial. While certain studies indicate that pericytes stay attached to the empty basement membrane of pruning vessels [88, 90, 96], others report that pericytes undergo apoptosis [7] or migrate into adjacent vessel segments [97, 98]. Further studies will be required in the future to determine the role and adaptive fate of pericytes during vessel pruning.

A role for immune cells in EC apoptosis and clearance during vessel pruning has also been reported. Leukocytes and cytotoxic T cells are able to induce EC death during retinal vessel pruning via CD95L [99]. During regression of the hyaloid vasculature, or during blood vessel pruning in the trachea of postnatal pups (upon anti-VEGF treatment), macrophages are also seen in close proximity to remodeling vessels. In these cases, they contribute to the passive clearance of apoptotic ECs [98, 100]. However, both in the embryo hindbrain and postnatal retina, macrophages additionally contribute to lumen formation and vessel remodeling by promoting vessel anastomosis [101]. This suggests that they might have dual roles or that different macrophage populations have distinct functions. In the zebrafish brain vasculature, microglia have also been shown to associate with pruning vessels after ECs underwent apoptosis, thus also indicating that they do not actively contribute to EC death, but rather to their removal afterwards [102]. While those studies indicate a fundamental role of the immune compartment in proper blood vessel development, further research is required to determine the extent of active and passive contribution of the immune compartment to vessel remodeling in different vascular beds.

Does EC apoptosis drive vessel pruning?

Whereas it is undebated that EC death accounts for the complete removal of fetal vascular systems, such as the hyaloid vasculature, different mechanisms might regulate partial vessel removal of a subset of vascular branches during postnatal development (vessel pruning). In addition to the studies mentioned above, where the potential contribution of pericytes and immune cell-driven induction of EC apoptosis and their contribution to vessel pruning were discussed [94, 95, 99, 101], one other hypothesis suggests that vessel pruning is primarily driven by EC migration and re-integration into neighboring vessel branches. We discuss below the contributions of both processes to postnatal vessel remodeling.

EC apoptosis has been implicated in certain conditions of vessel remodeling [90, 103–106] and in the regulation of capillary vessel diameter [12]. In the maturation phase of the retinal vasculature, characteristic avascular areas form around differentiating arteries. EC apoptosis is frequently observed in pruning vessels around arteries [12, 68, 88, 95] and several mouse mutants confirm a role of EC death in the regulation of vessel density. For example, mice lacking the pro-apoptotic BH3-only protein BIM [81] present increased vessel density in the retina. Loss of EC TIE1 [107] also leads to an increase in EC death and concomitant reduction in vessel density. A similar phenotype has been reported when regulators of the Wnt pathway, such as Gpr177 (required for wnt secretion) and Rspo3 (a wnt signaling enhancer) [90, 108] were knocked out in ECs. Interestingly, non-canonical Wnt signaling was further shown to regulate the response of ECs to shear stress, rather than cell death [109].

Even though EC death might affect vessel density, it is debated whether apoptosis under physiological conditions is required to initiate vessel pruning, as, despite a mild increase in the vascular area, vessel remodeling and maturation properly take place in the above-mentioned knockout mice and others. For example, even though EC apoptosis is increased in mice lacking the pro-survival protein MCL1, vessel regression is not affected [12]. In addition, vessel regression is unaffected in EC-specific Casp8 knockout mice [13], even though EC apoptosis is reduced. Furthermore, TRAIL^−/− mice only show a mild and transient increase in vessel density that is recovered at P5, and a small decrease in the capillary free area surrounding arteries [110]. In the developing rat retina, no correlation between vessel removal and EC apoptosis could be found [89]. Consistently, while the majority of apoptotic cells in the developing mouse and zebrafish retinal vasculature are found in pruning vessels, only a small subset of them (around 5% to 15%) contained apoptotic ECs [12, 88, 102]. Up to date, analysis of retina angiogenesis in Bak^−/− Bax^EC/EC mice (with full Bak, and EC-specific Bax deletion) has most directly evaluated the impact of EC death to vessel remodeling. Strikingly, Bak^−/− Bax^EC/EC knockout  with full inhibition of apoptosis via the intrinsic cell death signaling pathway in ECs, delayed, but did not prevent vessel pruning around arteries [12]. In the capillary region, where apoptosis is more scattered, blocking apoptosis did not have any effect on vessel pruning either [12].

Elegant time-lapse imaging studies in zebrafish have ultimately revealed in vivo that EC apoptosis is not common during vessel pruning [105, 111, 112]. Instead, ECs migrate out of remodeling vessels and reintegrate into neighboring vessel segments, thus eliminating the need for EC removal by cell death. In this model, changes in blood flow and the resulting impact on shear–stress are the driving forces for vessel pruning [111]. EC migration in response to hemodynamic cues also occurs in the mouse retina [88]. Interestingly, the sensitivity of ECs to flow depends on non-canonical wnt signaling, as in its absence ECs show an increased sensitivity to flow which results in premature vessel pruning [109].

One possible explanation linking the cell death and migration hypothesis could be that ECs that detach from the extracellular matrix during migration undergo cell death due to anoikis, which might explain why the majority of apoptotic ECs are found in remodeling vessels. In this case, EC apoptosis might not be the primary cause of vessel pruning, but consequence of cellular detachment or secondary to impaired blood flow [105]. It should be noted that TUNEL or cleaved CASP-3 positive cells have a short half-life and the commonly observed shedding of apoptotic ECs into the vascular lumen and their quick clearance by macrophages further complicates the precise evaluation of the kinetics of the above-mentioned processes. In addition, as our current knowledge of vessel remodeling is based on studies from both wildtype and mutant mice, caution should be taken by comparing physiologically and artificially induced vessel remodeling. Taken together, successful vessel pruning is likely a multi-step process involving EC migration, reintegration into neighboring vessels and a minor contribution of EC apoptosis.

Cell death-independent functions of the apoptosis signaling machinery in ECs

Accumulating evidences suggest that molecules of the cell death signaling machinery in ECs (and other cell types) can act beyond their classic apoptotic function. Deletion of TAK1 in ECs does not just lead to increased TNF-dependent EC apoptosis, but also to TNF-independent defects in EC migration [55]. Furthermore, the loss of the IAP survivin in ECs does not just lead to increased EC death in the developing embryo, but also to defects in neural tube closure. Those are not solely attributable to tissue hypoxia resulting from vascular malformations, but to cell death-independent changes in EC derived growth factor secretion that otherwise supports neural tube closure under physiological conditions [113]. Similarly, ECs of Casp8 knockout embryos display an enhanced cytokine expression profile, which is independent of RIPK3 and necroptosis [114]. These studies suggest that certain cell death signaling molecules also regulate additional, non-cell death-related EC properties and functions such as growth factor and cytokine expression, which might have fundamental roles during tissue development. They also raise the question of whether embryonic lethality in diverse knockout mice related to the cell death signaling pathway is solely due to dysregulated apoptosis/necroptosis or further supported by other, non-cell death related vascular dysfunctions.

During postnatal angiogenesis, several studies have shown that the pro-cell death signaling machinery does not promote apoptosis, but regulates vessel development independent of cell death. In contrast to many other cell types, the pro-apoptotic BH3-only protein PUMA, though strongly expressed in ECs [15], does not induce apoptosis [115]. Instead, it regulates EC proliferation, autophagy and blood vessel development in the retina via ERK signaling [15]. CD95 is also expressed in brain and retina ECs during postnatal development, and angiogenesis is delayed in EC-specific CD95 knockout mice [14]. In ECs, co-immunoprecipitation experiments revealed that CD95 interacts with SFK and p85. In line, CD95L stimulation of HUVECs leads to the phosphorylation and activation of Akt and ERK, and inhibition of Akt blocks CD95L induced EC proliferation [14]. In addition to its physiological role during angiogenesis in the central nervous system, activation of CD95 with the agonistic anti-CD95 mAb Jo2 was able to induce immune cell infiltration and angiogenesis in an in vivo Matrigel assay [116], indicating that CD95 signaling might also regulate inflammation induced angiogenesis. Recently, CASP-8 has also been shown to regulate angiogenesis in the retina in a cell death-independent way. Even though lethal during embryonic development, knockout of Casp8 in ECs during postnatal development did not affect mouse survival, thus indicating that after a critical time window of vasculogenesis and angiogenesis during embryonic development, postnatal ECs are more resistant to cell death in the absence of CASP-8. In fact, postnatal deletion of Casp8 in ECs only led to a mild delay in angiogenesis, which was dependent on RIPK3, but not MLKL and therefore necroptosis [13]. In line, RIPK1 and RIPK3 have been shown to positively regulate the response of ECs to VEGF stimulation in the bead sprouting assay, as inhibition of either of them ameliorated the VEGF induced sprouting response [117]. In both of the studies indicated above, this effect was mediated by increased p38 signaling, a known inhibitor of angiogenesis [118].

Even though the above-mentioned findings support a cell death-independent role of the cell death signaling machinery, the effect of death ligand stimulation of ECs per se in an in vitro setting is controversial and largely context dependent. Whereas some studies report that stimulation with TRAIL induces apoptosis in HUVECs [119] and has anti-angiogenic properties [120], other studies find that TRAIL stimulates angiogenesis [121]. In addition, and even in the absence of CASP-8, TNF-α and TRAIL (potent inducers of necroptosis in the absence of CASP-8 in other cell types [42, 122–124]) did not induce cell death in ECs in vitro [13]. Similar findings have been reported for CD95L. Even though CD95 is expressed on the surface of ECs, they are resistant to CD95L-induced cell death in vitro [125–127]. In HUVECs, this is mediated by association of monomeric CD95 with cMet and a strong expression and recruitment of c-FLIP to the DISC, therefore preventing CD95 oligomerization and DISC activation [128]. Interestingly, dimerized CD95 is detected when ECs lose matrix attachment and undergo anoikis [128] or when Akt signaling is inhibited [129], which highlights again that apoptosis might be a consequence, not cause, of vascular removal. To further explain why ECs seem surprisingly resistant to cell death, one study suggests that HUVECs treated with LPS secrete cleaved CASP-3 fragments into the supernatant, thus actively escaping from apoptosis [130]. Additional non-apoptotic, but barrier-promoting functions of CASP-3 have been reported in lung microvascular ECs [131]. Even though apoptosis was reported to be increased in the retina vasculature of Bcl2^−/− mice in vivo [83], isolated retina ECs from these mice did not show increased cell death under basal conditions but defects in cell adhesion, migration and capillary morphogenesis [132]. Thus, this data suggests that Bcl2^−/− ECs behave differently in processes of angiogenesis and that an environmental factor not present in culture would be required to induce apoptosis in vivo.

Taken together, these studies highlight the exceptional cell death-independent functions of the apoptosis machinery in ECs during physiological blood vessel formation. They further strengthen the hypothesis of a timely appropriate requirement of pro-survival factors, such as CASP-8, in the developing endothelium during the course of vessel formation.

EC death in pathology: a focus on oxygen induced retinopathy

ROP  and proliferative diabetic retinopathy (PDR) are diseases characterized by pathological EC apoptosis and vessel obliteration that is followed by an equally pathological boost of neo-vascularization which often results in the formation of disturbed and leaky vascular tufts [133, 134]. Vessels growing into the vitreous often lead to vision impairment, hemorrhage, scarring and in the worst case, retinal detachment [135]. ROP can be recapitulated in the oxygen-induced retinopathy (OIR) model in mice or rats [133, 134]. In this model, newborn mice are briefly exposed to hyperoxic conditions, which will lead to the regression of all capillaries in the central retina. Upon return to normal oxygen conditions, these areas become hypoxic, leading to increased production of proangiogenic factors, such as VEGF, PlGF and IGF-1 and thus pathological neoangiogenesis [136–138]. EC apoptosis accounts for the initial hyperoxia-induced vaso-obliteration, thus rendering the OIR model a useful system for the study of pathological EC death and regression [133, 139]. In addition, the malformed neo-vasculature undergoes spontaneous regression over time [85] which will eventually lead to the resolution of the vascular malformations. Similar to ROP, PDR is characterized by retinal–capillary non-perfusion that results in EC and pericyte apoptosis [140]. Again, this capillary loss results in the formation of focal ischemic-areas that induce an increased production of cytokines and pro-angiogenic factors such as VEGF-A , therefore resulting in increased pathological angiogenesis [141].

Several studies indicate that vaso-obliteration and EC apoptosis in the OIR model are regulated by the intrinsic cell death signaling pathway. Bim^−/− mice are resistant to hyperoxia induced vessel regression [81]. On the other hand, vaso-obliteration did not depend on BCL1, even though Bcl2^−/− mice presented a reduced amount of pathological neovascular tufts [83]. Strikingly, however, this phenotype was not recapitulated in EC specific Bcl-2^−/− mice, where vaso-obliteration was increased, but neovascularization unchanged compared to control littermates [142], indicating that BCL2 in other cell types also modulated OIR. More recently, it has been shown that revascularization in Bak^−/−Bax^EC/EC mice during OIR is increased. Even though ECs in these mice are protected from apoptosis, vessel obliteration and ischemia still occured. However, ECs within closed and unperfused vessels that were protected from apoptosis were able to rebuild a functional vascular system in response to pro-angiogenic stimulation faster compared to control mice, thus resulting in increased revascularization upon return to normoxia [143].

In contrast to its mild contribution to vessel pruning during physiological angiogenesis, the extrinsic cell death signaling pathway regulates EC death and vessel resolution in the OIR model. In the rat, treatment with a CD95L-neutralizing antibody reduced vaso-obliteration in the OIR model [99]. However, CD95L loss of function mice (Fasl^gld/gld) show normal vaso-obliteration in the OIR model, but the formation of neovascular tufts was increased [144, 145]. This was accompanied by having fewer TUNEL + cells in the tuft areas, indicating that CD95 signaling might limit pathologic neovascularization by inducing EC apoptosis. TRAIL^−/− mice did not show any impairment in vaso-obliteration, however, similar to Fasl^gld/gld mutant mice, neovascularization was increased [110]. Furthermore, tuft regression was delayed, indicating that TRAIL was required to limit both excessive neovascularization and to promote resolution of malformed vessels. Consistent with its role as a pro-survival factor, vaso-obliteration in the OIR model was increased in EC specific Casp8 knockout mice [13]. Of benefit, as CASP-8 regulates angiogenesis in a cell death-independent way, tuft formation was also decreased in the OIR model [13], suggesting that regulating CASP-8 in ECs could be beneficial for inducing or preventing vessel growth.

Taken together, our knowledge based on studies of the OIR model indicates that EC apoptosis can be a major contributor to neovascular diseases such as ROP and PDR. It should be noted that ROP is unique and different from other pathological neovascular conditions, as the vessels in the developing retina are still immature and thus dependent on VEGF signaling. In line, adult mice are resistant to OIR. This is consistent with, for example, the timely role of BCL2 and CASP-8 in early development, as discussed before. Hence, it also supports the finding that ECs possess a differential sensitivity and phenotypic outcome towards cell death by different signaling pathways. The above-mentioned studies, together with the fact that the extrinsic cell death signaling pathway also regulates cytokine production and thus potentially inflammation driven neo-angiogenesis, highlight the complex contribution of death receptor regulated signaling in ECs during pathological angiogenesis—a novel field that requires further investigation.

Targeting the cell death signaling machinery in ECS during tumor angiogenesis

Growing tumors become vascularized with blood vessels to promote tumor oxygenation, nutrient delivery and ultimately metastatic spread [146]. Anti-angiogenic tumor therapy initially aimed to ‘starve tumors to death’ by inducing massive vessel regression [147]. Similar to physiological vessel development, TIE-1, EVI (the protein encoded by Gpr177) and R-spondin-3 have been shown to promote tumor angiogenesis. Therefore, deletion of these pro-survival factors in ECs has been shown to reduce tumor angiogenesis in B16-xenograft and lewis lung carcinoma (LLC) models [90, 107, 108]. In addition, as a subset of tumor vessels in expanding tumors remains immature, VEGF withdrawal strategies might be exploited, similar to treatment of ROP, for enforcing vessel regression [148]. However, as already indicated, these treatments only target the most immature vessels, while leaving behind a more mature and stable vascular network [149]. Therefore, new strategies are required to promote full regression of the tumor vasculature.

Whereas activation of the cell death signaling machinery in tumor cells has been in the center of anti-cancer therapy in the last decades [150, 151], studies targeting cell death signaling pathways in ECs to force vessel regression are just recently starting to emerge. Hereby, targeting TAK1 (which is known to inhibit apoptosis) in ECs seems to be a promising strategy. Specific deletion of TAK1 in ECs significantly reduced tumor growth in an EL4 lymphoma and LLC model that form tumors that are refractory to anti-VEGF therapy [18, 152]. Deletion of TAK1 after the tumor had already formed also lead to a significant regression of the tumor tissue due to increased EC apoptosis. However, vascular leakage, hemorrhage formation, and tumor hypoxia were increased [18]. Another study reported that TAK1 deletion induced EC necroptosis and, therefore, increased metastatic spread, as tumor cell extravasation was promoted in the leaky vasculature [153]. Consistently, several other studies have reported that EC necroptosis, or activation of the necroptosis signaling machinery in ECs, rather favor metastatic spread. For example, tumor cells extravasate by inducing necroptosis of ECs via DR6, which is further increased in EC specific Casp8 knockout mice, where induction of necroptosis is facilitated [154]. In contrast, inhibition of RIPK1 and RIPK3 reduces metastasis formation and vascular leakage, even though contradictory data exists on whether this is via inhibition of necroptosis, or inhibition of cell death-independent functions of RIP-kinases [117, 154].

Taken together, EC death in the tumor vasculature clearly has its advantages and disadvantages and further studies are required to decipher the potential of induced EC death in cancer therapy. Hereby, it is likely that its effects might be different in the primary tumor and sites of tumor metastasis and also depend on the precise cell death modality, for example EC apoptosis vs. necroptosis.

Conclusions and future perspective

A collection of numerous studies over the last 20 years has shaped our understanding of EC death during blood vessel development and also significantly contributed to our knowledge about pathological EC death to diseases such as ROP. Taken together, those studies highlight the differential function of cell death signaling molecules in ECs during these processes (Fig. 2). Yet, it is important to note that most of our interpretations are based on studies in the mouse retina. Therefore, further research is required to understand the differential contribution of EC death in different vascular beds and different developmental stages: How is it possible, that the same pro-survival factors, such as CASP-8, are essential during vessel formation in the embryo, but dispensable at later developmental stages? And what is controlling the switch from a deathly cell death signaling machinery to the proangiogenic functions of the same molecules?

Fig. 2.

Contribution and function of cell death signaling molecules in ECs during vessel development and pathology. Apoptosis-related molecules can act in a cell death-dependent and -independent manner in ECs. Red lightnings symbols indicate negative effects, and light bulbs symbol indicates positive effects, of increased cell death signaling in ECs.

In this context, the role of vessel-associated cells, such as pericytes and macrophages that could substantially alter the sensitivity of ECs to cell death requires further attention. In addition, regulation of differential cell behavior by the physical properties of the environment, for example by the extracellular matrix (ECM) is gaining increasing attention. To answer these questions, improved invivo systems, combined with mathematical modeling, are required to study the interaction of ECs within the vessel sprout and its surrounding tissue during angiogenesis to precisely define the timely manner of EC migration, apoptosis, and vessel pruning.

Last but not least, further work is required to translate our knowledge of EC death under physiological conditions to pathological vessel regression. Do they follow the same mechanistic principles? And is the cell death signaling machinery required to maintain physiological vessel homeostasis in the quiescent, adult vasculature? Answering these questions  will contribute to the fundamental understanding of the mechanisms regulating vessel formation and will contribute to develop and improve the efficacy of anti-angiogenic therapies.

Abbreviations

EC

Endothelial cell

OIR

Oxygen-induced retinopathy

Funding

Open Access funding enabled and organized by Projekt DEAL. This work was supported by ERC-CoG (864875); by a grant of the Deutsche Forschungsgemeinschaft (DFG) from FOR2325 (“Interactions at the Neurovascular Interface”); a DFG grant from SFB1366 (“Vascular control of Organ Function” project number 39404578) and by a grant from the Rolf. M. Schwiete Foundation.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no competing interests.