Serum-free media and the immunoregulatory properties of mesenchymal stem cells in vivo and in vitro

Cell Physiol Biochem. 2014;33(3):569-80. doi: 10.1159/000358635. Epub 2014 Feb 25.

Abstract

Background: Mesenchymal stem cells are capable of self-renewal and multi-lineage differentiation. They are used extensively to treat several diseases. Traditionally, mesenchymal stem cells are cultured in serum-containing media, typically supplemented with fetal bovine serum (FBS). However, the variability of FBS is likely to skew experimental results. Although serum-free media used to expand mesenchymal stem cells has facilitated remarkable achievements, immunomodulation of these cells in under serum-free conditions is poorly understood. We hypothesized that mesenchymal stem cells expanded in serum-free media will retain powerful immunoregulatory functions in vitro and in vivo.

Design and methods: Immunosuppressive activity and the immunomodulatory cytokines produced by mesenchymal stem cells in serum-free media were characterized in vitro. Immunomodulation by serum-free mesenchymal stem cell expansion in monocrotaline-induced pulmonary hypertension was explored in vivo.

Results: Similar to cells in serum-containing media, mesenchymal stem cells expanded in serum-free media inhibited proliferation and apoptosis of CD4(+)T cells. They also exhibited strong immunosuppressive activities and secreted high levels of immunomodulatory cytokines such as PGE2, IDO1, COX2, IL-6, and IL-1β, but not HGF. On the other hand, growth of mesenchymal stem cells in serum-free media attenuated pulmonary vascular remodeling and inhibited mRNA expression of proinflammatory cytokines TNF-α, IFN-γ, IL-6, IL-1β, and IL-18.

Conclusions: Mesenchymal stem cells in serum-free media maintained powerful immunomodulatory function in vitro and in vivo; serum-free media may replace serum-containing media for basic research and clinical applications.

MeSH terms

  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / immunology
  • CD4-Positive T-Lymphocytes / immunology*
  • Cattle
  • Cell Proliferation / drug effects*
  • Culture Media, Serum-Free / pharmacology*
  • Cyclooxygenase 2 / immunology
  • Cytokines / immunology
  • Dinoprostone / immunology
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / immunology
  • Humans
  • Immune Tolerance / drug effects*
  • Indoleamine-Pyrrole 2,3,-Dioxygenase / immunology
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / immunology*

Substances

  • Culture Media, Serum-Free
  • Cytokines
  • IDO1 protein, human
  • Indoleamine-Pyrrole 2,3,-Dioxygenase
  • Cyclooxygenase 2
  • PTGS2 protein, human
  • Dinoprostone