hASC and DFAT, Multipotent Stem Cells for Regenerative Medicine: A Comparison of Their Potential Differentiation In Vitro

Int J Mol Sci. 2017 Dec 13;18(12):2699. doi: 10.3390/ijms18122699.

Abstract

Adipose tissue comprises both adipose and non-adipose cells such as mesenchymal stem cells. These cells show a surface antigenic profile similar to that of bone-marrow-derived MSC. The cells derived from the dedifferentiation of mature adipocytes (DFAT) are another cell population with characteristics of stemness. The aim of this study is to provide evidence of the stemness, proliferation, and differentiation of human adipose stem cells (hASC) and DFAT obtained from human subcutaneous AT and evaluate their potential use in regenerative medicine. Cell populations were studied by histochemical and molecular biology techniques. Both hASC and DFAT were positive for MSC markers. Their proliferative capacity was similar and both populations were able to differentiate into osteogenic, chondrogenic, and adipogenic lineages. DFAT were able to accumulate lipids and their lipoprotein lipase and adiponectin gene expression were high. Alkaline phosphatase and RUNX2 gene expression were greater in hASC than in DFAT at 14 days but became similar after three weeks. Both cell populations were able to differentiate into chondrocytes, showing positive staining with Alcian Blue and gene expression of SOX9 and ACAN. In conclusion, both hASC and DFAT populations derived from AT have a high differentiation capacity and thus may have applications in regenerative medicine.

Keywords: adipocytes; adipose tissue; cell culture in vitro; dedifferentiated fat adipose tissue; fibroblast-like; human adipose stem cells.

MeSH terms

  • Adipose Tissue / cytology
  • Aged
  • Aggrecans / metabolism
  • Alkaline Phosphatase / genetics
  • Alkaline Phosphatase / metabolism
  • Antigens, CD / metabolism
  • Cell Dedifferentiation
  • Cell Differentiation / physiology*
  • Cells, Cultured
  • Core Binding Factor Alpha 1 Subunit / genetics
  • Core Binding Factor Alpha 1 Subunit / metabolism
  • Female
  • Humans
  • Male
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Middle Aged
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / metabolism
  • Osteogenesis
  • Regenerative Medicine*
  • SOX9 Transcription Factor / metabolism

Substances

  • ACAN protein, human
  • Aggrecans
  • Antigens, CD
  • Core Binding Factor Alpha 1 Subunit
  • RUNX2 protein, human
  • SOX9 Transcription Factor
  • Alkaline Phosphatase