VEGF-mediated proliferation of human adipose tissue-derived stem cells

PLoS One. 2013 Oct 3;8(10):e73673. doi: 10.1371/journal.pone.0073673. eCollection 2013.

Abstract

Human adipose tissue-derived stem cells (ADSCs) are an attractive multipotent stem cell source with therapeutic applicability across diverse fields for the repair and regeneration of acute and chronically damaged tissues. In recent years, there has been increasing interest in ADSC for tissue engineering applications. However, the mechanisms underlying the regulation of ADSC proliferation are not fully understood. Here we show that 47 transcripts are up-regulated while 23 are down-regulated in ADSC compared to terminally differentiated cells based on global mRNA profiling and microRNA profiling. Among the up-regulated genes, the expression of vascular endothelial growth factor (VEGF) is fine-tuned by miR-199a-5p. Further investigation indicates that VEGF accelerates ADSC proliferation whereas the multipotency of ADSC remains stable in terms of adipogenic, chondrogenic and osteogenic potentials after VEGF treatment, suggesting that VEGF may serve as an excellent supplement for accelerating ADSC proliferation during in vitro expansion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Adipogenesis / drug effects
  • Adipose Tissue / cytology*
  • Cell Proliferation / drug effects
  • Chondrogenesis / drug effects
  • Gene Expression Profiling
  • Gene Expression Regulation / drug effects
  • Genomics
  • Humans
  • MicroRNAs / genetics
  • Multipotent Stem Cells / cytology*
  • Multipotent Stem Cells / drug effects
  • Multipotent Stem Cells / metabolism
  • Osteogenesis / drug effects
  • Vascular Endothelial Growth Factor A / genetics
  • Vascular Endothelial Growth Factor A / metabolism*
  • Vascular Endothelial Growth Factor A / pharmacology

Substances

  • 3' Untranslated Regions
  • MicroRNAs
  • Vascular Endothelial Growth Factor A

Grants and funding

This work was supported by the Ministry of Science and Technology of China (2010CB945600, 2010CB944901, 2011CB965100), the National Natural Science Foundation of China (91019017, 81202550, 81100673, 81070738), Shanghai Science Foundation (#11PJ1407800), the Ministry of Education of China (IRT1168), Shenzhen Science and Technology Innovation Committee (JCYJ20120613172906373), and the Program for Eastern Scholar at Shanghai. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.