Improvement of human pancreatic islet quality after co-culture with human adipose-derived stem cells

Mol Cell Endocrinol. 2020 Apr 5:505:110729. doi: 10.1016/j.mce.2020.110729. Epub 2020 Jan 21.

Abstract

The aim of this study was to investigate whether co-culture of human islets with adipose-derived stem cells (ASCs) can improve islet quality and to evaluate which factors play a role in the protective effect of ASCs against islet dysfunction. Islets and ASCs were cultured in three experimental groups for 24 h, 48 h, and 72 h: 1) indirect co-culture of islets with ASC monolayer (Islets/ASCs); 2) islets alone; and 3) ASCs alone. Co-culture with ASCs improved islet viability and function in all culture time-points analyzed. VEGFA, HGF, IL6, IL8, IL10, CCL2, IL1B, and TNF protein levels were increased in supernatants of islet/ASC group compared to islets alone, mainly after 24 h. Moreover, VEGFA, IL6, CCL2, HIF1A, XIAP, CHOP, and NFKBIA genes were differentially expressed in islets from the co-culture condition compared to islets alone. In conclusion, co-culture of islets with ASCs promotes improvements in islet quality.

Keywords: Adipose-derived stem cells; Co-culture; Cytokines; Gene expression; Pancreatic islets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / cytology*
  • Apoptosis / drug effects
  • Apoptosis / genetics
  • Chemokines / metabolism
  • Coculture Techniques
  • Culture Media
  • Endoplasmic Reticulum Stress / drug effects
  • Endoplasmic Reticulum Stress / genetics
  • Gene Expression Regulation / drug effects
  • Humans
  • Inflammation / genetics
  • Inflammation Mediators / metabolism
  • Insulin / pharmacology
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Islets of Langerhans / cytology*
  • Neovascularization, Physiologic / drug effects
  • Neovascularization, Physiologic / genetics
  • Stem Cells / cytology*
  • Stem Cells / drug effects
  • Time Factors
  • Tissue Survival / drug effects

Substances

  • Chemokines
  • Culture Media
  • Inflammation Mediators
  • Insulin
  • Intercellular Signaling Peptides and Proteins