Umbilical cord mesenchymal stem cells suppress B-cell proliferation and differentiation

Cell Immunol. 2012;274(1-2):46-53. doi: 10.1016/j.cellimm.2012.02.004. Epub 2012 Feb 23.

Abstract

Mesenchymal stem cells (MSCs) may be obtained from umbilical cord as an abundant and noninvasive source. However, the immunomodulatory properties of umbilical cord-MSCs (UC-MSCs) were poorly studied. In this study, we aimed to investigate the effects of UC-MSCs on B-cell proliferation and differentiation. UC-MSCs were found to suppress the proliferation of B cells isolated from murine spleen. Moreover, UC-MSCs markedly suppressed B-cell differentiation as shown by the decreased number of CD138+cells and reduced levels of IgM and IgG production in coculture. As revealed by transwell experiments, soluble factors produced by UC-MSCs might be involved in mediating B-cell suppression. The Blimp-1 mRNA expression was suppressed whereas the PAX-5 mRNA expression was induced in coculture. Finally, UC-MSCs modified the phosphorylation pattern of Akt and p38 pathways, which were involved in B-cell proliferation and differentiation. These results may further support the potential therapeutic use of UC-MSCs in treating autoimmune disorders.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Coculture Techniques
  • Female
  • Immunoglobulin G / biosynthesis
  • Immunoglobulin M / biosynthesis
  • Mesenchymal Stem Cells / immunology*
  • Mice
  • Mice, Inbred C57BL
  • PAX5 Transcription Factor / biosynthesis*
  • PAX5 Transcription Factor / genetics
  • Phosphorylation
  • Positive Regulatory Domain I-Binding Factor 1
  • Proto-Oncogene Proteins c-akt / metabolism
  • RNA, Messenger / biosynthesis
  • Syndecan-1 / biosynthesis
  • Transcription Factors / biosynthesis*
  • Transcription Factors / genetics
  • Umbilical Cord / immunology
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Immunoglobulin G
  • Immunoglobulin M
  • PAX5 Transcription Factor
  • Pax5 protein, mouse
  • Prdm1 protein, mouse
  • RNA, Messenger
  • Syndecan-1
  • Transcription Factors
  • Positive Regulatory Domain I-Binding Factor 1
  • Proto-Oncogene Proteins c-akt
  • p38 Mitogen-Activated Protein Kinases