Adipose-Derived Stem Cells in Reinforced Collagen Gel: A Comparison between Two Approaches to Differentiation towards Smooth Muscle Cells

Int J Mol Sci. 2023 Mar 16;24(6):5692. doi: 10.3390/ijms24065692.

Abstract

Scaffolds made of degradable polymers, such as collagen, polyesters or polysaccharides, are promising matrices for fabrication of bioartificial vascular grafts or patches. In this study, collagen isolated from porcine skin was processed into a gel, reinforced with collagen particles and with incorporated adipose tissue-derived stem cells (ASCs). The cell-material constructs were then incubated in a DMEM medium with 2% of FS (DMEM_part), with added polyvinylalcohol nanofibers (PVA_part sample), and for ASCs differentiation towards smooth muscle cells (SMCs), the medium was supplemented either with human platelet lysate released from PVA nanofibers (PVA_PL_part) or with TGF-β1 + BMP-4 (TGF + BMP_part). The constructs were further endothelialised with human umbilical vein endothelial cells (ECs). The immunofluorescence staining of alpha-actin and calponin, and von Willebrand factor, was performed. The proteins involved in cell differentiation, the extracellular matrix (ECM) proteins, and ECM remodelling proteins were evaluated by mass spectrometry on day 12 of culture. Mechanical properties of the gels with ASCs were measured via an unconfined compression test on day 5. Gels evinced limited planar shrinkage, but it was higher in endothelialised TGF + BMP_part gel. Both PVA_PL_part samples and TGF + BMP_part samples supported ASC growth and differentiation towards SMCs, but only PVA_PL_part supported homogeneous endothelialisation. Young modulus of elasticity increased in all samples compared to day 0, and PVA_PL_part gel evinced a slightly higher ratio of elastic energy. The results suggest that PVA_PL_part collagen construct has the highest potential to remodel into a functional vascular wall.

Keywords: adipose tissue-derived stem cells; collagen particles; endothelial cells; extracellular matrix; gel reinforcement; remodelling; stem cells differentiation; tissue engineering; vascular patches.

MeSH terms

  • Adipose Tissue*
  • Animals
  • Cell Differentiation
  • Cells, Cultured
  • Collagen* / metabolism
  • Extracellular Matrix Proteins / metabolism
  • Gels / metabolism
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Myocytes, Smooth Muscle / metabolism
  • Stem Cells / metabolism
  • Swine
  • Tissue Engineering / methods

Substances

  • Collagen
  • Extracellular Matrix Proteins
  • Gels

Grants and funding

This research was funded by the Czech Health Research Council, the Ministry of Health of the Czech Republic, Grant Nos. NV19-02-00068 and NV18-01-00332 and by the European Union—Next Generation EU, the project National Institute for Research of Metabolic and Cardiovascular Diseases, Programme EXCELES, ID Project No. LX22NPO5104. We also acknowledge the Light Microscopy Core Facility, IMG CAS, IPHYS CAS, Prague, Czech Republic, supported by MEYS CR, Grant No. LM2018129 Czech-BioImaging, by ERDF, Grant No. CZ.02.1.01/0.0/0.0/18_046/0016045 and by RVO, Grant No. 68378050-KAV-NPUI, for their support with the confocal/widefield/superresolution imaging/image analysis presented herein. Microscopy was performed in the Vinicna Microscopy Core facility, co-financed by the Czech-BioImaging large RI project LM2018129, funded by MEYS CR. Computational resources were supplied by the MEYS CR, the project “e-Infrastruktura CZ” (e-INFRA LM2018140), provided within the program Projects of Large Research, Development, and Innovations Infrastructures. Projekt: Transformace pro VŠ na UK, specifický cíl A, NPO_UK_MSMT-16602/2022.