Comparative analysis of mesenchymal stromal cells from murine bone marrow and amniotic fluid

Cytotherapy. 2007;9(8):729-37. doi: 10.1080/14653240701656061. Epub 2007 Oct 5.

Abstract

Background: Murine mesenchymal stromal cells (mMSC) are a good model for pre-clinical investigations, and alternative sources of mMSC are subject to intensive experiments. In the present study, we obtained mMSCs from amniotic fluid (AF) and compared their characteristics with mMSCs from bone marrow (BM).

Methods: NMRI mice, 4-6 weeks old, were killed and AF and BM cells collected from those in the second week of pregnancy. MSC were achieved by adhesion to cell culture plastic. Isolated cells were assessed for clonogenic capacity, some surface markers (epitopes) and differentiation potential.

Results: We achieved AF mMSC more readily than BM mMSC. Differences concerning colony assay and some surface markers of mMSC derived from these two source cells were observed. Most strikingly, AF mMSC showed no adipogenic differentiation capacity, in contrast with BM mMSC.

Discussion: Our results show that mMSC from AF are an appropriate source for pre-clinical investigation. Furthermore, mMSC from different sources of mice vary in clonogenic capacity, surface markers and differentiation potential.

Publication types

  • Comparative Study

MeSH terms

  • Adipogenesis
  • Amniotic Fluid / cytology*
  • Animals
  • Antigens, CD34
  • Antigens, Differentiation
  • Bone Marrow Cells / physiology
  • Cell Culture Techniques
  • Cell Differentiation
  • Cell Lineage
  • Cell Separation
  • Colony-Forming Units Assay
  • Female
  • GATA2 Transcription Factor / metabolism
  • Mesenchymal Stem Cells* / cytology
  • Mesenchymal Stem Cells* / physiology
  • Mice
  • Octamer Transcription Factor-3 / metabolism
  • Pregnancy
  • Stromal Cells* / cytology
  • Stromal Cells* / physiology

Substances

  • Antigens, CD34
  • Antigens, Differentiation
  • GATA2 Transcription Factor
  • Octamer Transcription Factor-3