Table 2.
Device characteristics | Barrier characterization methods | Supplementary information | |||||||||
---|---|---|---|---|---|---|---|---|---|---|---|
Target disease | Chip type | Channel design | Culture type and ECM | Cell type(s) | Disease induction method | TEER Sensors | Permeability assessment | Immunostaining | Major on-chip disease phenotypes | Importance/Applications | Ref |
AD | PDMS-based microfluidic chip (dynamic) | Parallel channels separated by post array | EC: 2D with Matrigel; Brain: 3D with Matrigel and collagen type I gel | EC: hCMEC/D3; Brain: ReN cells | ReN cell line with human familial AD mutations | NA | 3kDa and 40kDa dextrans | Claudin-1, Claudin-5, VE-cadherin | Increased permeability; reduced TJ expression; in vivo like Aβ deposition patterns; Neuronal damage due to neurotoxins | Modeling of AD pathologies in vitro using BBB-on-a-chip model with genetically modified ReN cells | [170] |
ALS | PDMS-based microfluidic chip (dynamic) | Custom design | EC: 2D with collagen type I gel; Motor unit: 3D with MN spheroids and collagen type I gel/Matrigel | EC: iPSC-ECs; Motor unit: patient-derived hESC- and iPSC-MNs, iPSC-skeletal muscle cells, | Addition of excess glutamic acid; patient-derived cells | NA | 40kDa dextran | ZO-1, occludin, P-glycoprotein | Decreased muscle contraction; muscle function improved by cotreatment with rapamycin and bosutinib through BBB | ALS-on-a-chip using cells from ALS patients and demonstration of compromised muscle function in ALS vs. control model | [225] |
GBM | PDMS-based microfluidic chip (dynamic) | Central chamber (brain) and outer channel (EC barrier) | EC & Brain: 2D with Matrigel/fibronectin | EC: HUVECs; Brain: CTX-TNA2 rat brain astrocytes, and Met-1 murine metastatic breast cancer cells | Mouse-derived primary cancer cells | NA | 3kDa and 70kDa dextrans; Rho 123; sulforhodamine 101 Acid Chloride | NA | Increased permeability | One of the first BTB-on-a-chip platforms; demonstration of leakier barrier phenotype in BTB vs BBB model | [226] |
PDMS-based microfluidic + bioprinted chip (dynamic) | Central chamber (brain) and outer channel (EC barrier) | EC: 2D with fibronectin; Brain: 3D in GelMA-alginate and GelMA-fibrin hydrogels | EC: hCMEC/D3 or HUVECs; Brain: human GBM cells | Cancer cell line | NA | 40kDa Texas Red-dextran | ZO-1 | Decreased ZO-1 expression in hCMEC/D3; alteration of cell morphology and decreased expression of vinculin and active Yap1 in GBM cells with microgravity exposure | A dynamic, microfluidic GBM-on-a-chip with bioprinted GBM; elucidation of effects of mechanical cues on BTB and GBM cells | [178] | |
PDMS-based microfluidic chip (dynamic) | Parallel channels separated by post array | EC & Brain: 3D with fibrinogen | EC: HUVEC; Brain: U-87, patient-derived GBM cells | Cancer cell line; patient-derived cells | NA | 70 kDa dextran | Green fluorescent protein, VE-cadherin, vWF | Colocalization of GBM stem-like cells with perivascular niche; distinct migration trajectory profiles for different GBM cell lines with accompanying changes in gene expression | Recapitulation of 3D microvasculature in GBM; a new potential functional assay to assess the invasiveness of GBM cells for personalized medicine | [227] | |
PDMS-based microfluidic chip (dynamic) | Central chamber (brain) and outer channel (EC barrier) | EC: 2D with Poly-D-Lysine; Brain: 3D with Matrigel and HA |
EC: hBMECs; Brain: macrophages, microglia, CD8+ T-cells, and patient-derived GBM cells |
Patient-derived cells | NA | NA | NA | Distinct profiles of T cell extravasation, cytotoxic activities, PD-1 expression, and inflammatory cytokine secretion between different GBM subtypes | Development of a patient-specific GBM model that differentiates different GBM subtypes; Enables personalized molecular assessment of effects of anti-PD1 therapy | [228] | |
HD | PDMS-based microfluidic chip (dynamic) | Sandwiched channels with top (brain) and bottom (vascular) chambers | EC: 2D with collagen IV and fibronectin; Brain: 3D with EZ-spheres and laminin | EC: iPSC-BMECs; Brain: iPSC-EZ spheres | Patient-derived cells | Integrated Au electrodes (AC resistance) | 4, 20 or 70 kDa dextrans; 3,5,3'-triiodothyronine; 2-NBDG; retigabine; levetiracetam; colchicine | GLUT-1, PECAM-1, Caudin-5, Occludin, ZO-1 | Increased permeability with inter-individual variations | Development of BBB-on-a-chip that captures in vivo like complexity of BBB and recapitulates patient heterogeneity in HD phenotype | [65] |
PD | PDMS-based microfluidic chip (dynamic) | Sandwiched channels with top (brain) and bottom (vascular) chambers | EC & Brain: 2D with collagen type IV, fibronectin, and laminin |
EC: iPSC-BMECs; Brain: primary human brain pericytes, primary human astrocytes, primary human brain microglia, iPSC-neurons |
Treatment with αSyn fibril | NA | 3 kDa dextran, and 0.5 kDa lucifer yellow | Claudin-1, Claudin-5, Occludin, PECAM-1 | Phosphorylation of αSyn129, decreased mitochondrial activity and increase in ROS production, induction of caspase-3 activation and neuroinflammation; increased permeability | Recapitulation of PD pathologies induced by treatment with αSyn fibril in BBB-on-a-chip system | [229] |
Stroke | PDMS-based microfluidic chip (dynamic) | Parallel channels separated by a smaller middle channel | EC:2D; Brain: 3D with Engelbreth–Holm–Swarm tumor (Cultrex) |
EC: human primary BMECs; Brain: human primary astrocytes, human microglial cell line, human primary vascular pericytes, iPSC-NPCs |
Treatment with low oxygen and deprivation of serum and glucose content | Chopstick silver chloride electrodes (DC resistance) | 4kDa and 70kDa dextrans | PECAM-1, vWF, ZO-1, Claudin-5 | Upregulation of inflammatory genes; increased activity of glutamate and decreased activity of GABA; irregular Ca2+ signaling patterns; increased VEGF; decreased TJ protein expression; pericyte and microglia activation; disruption of AQP4 | Development of stroke-on-a-chip; assessed the neurorestorative effects of several stem cell-based therapies | [177] |