Adipose stem cell-derived extracellular matrix represents a promising biomaterial by inducing spontaneous formation of prevascular-like structures by mvECs

Biotechnol Bioeng. 2020 Oct;117(10):3160-3172. doi: 10.1002/bit.27481. Epub 2020 Jul 15.

Abstract

Tissue constructs of physiologically relevant scale require a vascular system to maintain cell viability. However, in vitro vascularization of engineered tissues is still a major challenge. Successful approaches are based on a feeder layer (FL) to support vascularization. Here, we investigated whether the supporting effect on the self-assembled formation of prevascular-like structures by microvascular endothelial cells (mvECs) originates from the FL itself or from its extracellular matrix (ECM). Therefore, we compared the influence of ECM, either derived from adipose-derived stem cells (ASCs) or adipogenically differentiated ASCs, with the classical cell-based FL. All cell-derived ECM (cdECM) substrates enabled mvEC growth with high viability. Prevascular-like structures were visualized by immunofluorescence staining of endothelial surface protein CD31 and could be observed on all cdECM and FL substrates but not on control substrate collagen I. On adipogenically differentiated ECM, longer and higher branched structures could be found compared with stem cell cdECM. An increased concentration of proangiogenic factors was found in cdECM substrates and FL approaches compared with controls. Finally, the expression of proteins associated with tube formation (E-selectin and thrombomodulin) was confirmed. These results highlight cdECM as promising biomaterial for adipose tissue engineering by inducing the spontaneous formation of prevascular-like structures by mvECs.

Keywords: adipose-derived stem cells; biomaterials; extracellular matrix; prevascular-like structures; tissue engineering.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / blood supply
  • Adipose Tissue / cytology*
  • Biocompatible Materials / chemistry*
  • Cell Differentiation / physiology
  • Cells, Cultured
  • Endothelial Cells / cytology*
  • Extracellular Matrix / chemistry*
  • Extracellular Matrix / metabolism
  • Humans
  • Neovascularization, Physiologic
  • Stem Cells / cytology*

Substances

  • Biocompatible Materials