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. Author manuscript; available in PMC: 2020 Nov 10.
Published in final edited form as: Adv Healthc Mater. 2019 Feb 4;8(5):e1801217. doi: 10.1002/adhm.201801217

Table 5.

Combinatorial soluble dECM-biomaterial scaffolds.

dECM source Additional material Cell source Findings References
Porcine cECM GelMA Human neonatal CPCs Improved cardiac commitment, endothelial commitment, angiogenic potential compared to pure GelMA patches Neovascularization following 14 d implantation [103]
Collagen I Human ESCs Higher cECM content improved cardiac commitment [112,113]
Chitosan Murine CMs Improved cardiac commitment, retention, conduction velocities, contractile stress compared to gelatin-chitosan [116]
Chitosan, PCL core None Induced M2 macrophages in vivo [117]
Silk Human ESCs and ESC-derived CMs Anisotropic, aligned fibers formed via oriented freezing Improved cardiac commitment compared to aligned or isotropic silk
cECM inclusion improved cell infiltration and vascularization in vivo
[120]
Silk Murine cardiac fibroblasts Silk/cECM concentration tailors mechanical properties and fibroblast proliferation, viability, integrin expression [121]
PEG-acrylate Murine fibroblasts Increased cECM scaffold modulus Fibroblasts remained viable with inclusion of PEG [93]
PLGA Human MSCs Tissue papers induced MSC proliferation [122]
PCL and VEGF Human CPCs and MSCs Patterned patches improved angiogenesis and ejection fraction in rat MI model [123]
Human cECM Amniotic membrane Human cardiac fibroblasts, epicardial cells, CMs CMs showed improved adhesion and survival compared to pure amniotic membrane
Reduced monocyte secretion of inflammatory cytokines and induction of M1 macrophages
[114]
Murine cECM (fetal and adult) Fibrin and transglutaminase Human CPCs CPCs remained viable and showed cardiac commitment [115]
Bovine cECM Chitosan Human CPCs Higher cECM ratio improves CPC viability [118]
Porcine pECM Chitosan Human MSCs Cardiac preservation and increase in cardiac function 8 weeks postinjection in MI model [119]
Ovine pECM CNTs Murine CMs CNTs suppressed CM cytotoxicity Improved proliferation, gap junction expression, and contraction compared to pECM hydrogels or gelatin-fibronectin-coated plates [124]