Selection of CD271(+) cells and human AB serum allows a large expansion of mesenchymal stromal cells from human bone marrow

Cytotherapy. 2009;11(2):153-62. doi: 10.1080/14653240802582125.

Abstract

Background: Mesenchymal stromal cells (MSC) are promising candidates for cell therapy and tissue engineering and may be used to treat acute graft-versus-host disease (GvHD). However, major obstacles for their clinical use are the required cell dose and the biosafety and potential immunogenicity of fetal bovine serum (FBS), which is a crucial supplement of all media currently used for the culture of MSC.

Methods: In this study MSC were successfully expanded after selection of CD271 cells from human bone marrow (BM) mononuclear cells in medium supplemented with 10% pooled allogeneic human serum.

Results: We isolated MSC from 10 healthy donor BM by plastic adherence and immunomagnetic selection of the CD271(+) fraction and expanded MSC in medium supplemented with pooled human allogeneic serum and animal serum. We isolated a homogeneous multipotent population by CD271(+) selection with a proliferation rate that was higher than MSC isolated by plastic adherence, 6.8+/-1.57 compared with 2.07+/-1.40 logs. Similar to cells generated in animal serum medium, MSC from allogeneic human serum were positive for mesenchymal markers and negative for hematopoietic markers; moreover they expressed embryonic stem cell genes. A normal karyotype and differentiation capacity into adipogenic, osteogenic and chondrogenic lineages and neurosphere-like structures were preserved throughout long-term culture.

Discussion: Expansion of MSC is both feasible and large with a CD271-selected population in medium supplemented with 10% pooled allogeneic human serum, without loss of multipotent differentiation capacity or karyotype alterations.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / genetics
  • Antigens, Differentiation / metabolism
  • Bone Marrow Cells / cytology*
  • Cattle
  • Cell Adhesion
  • Cell Differentiation
  • Cell Lineage
  • Cell Proliferation*
  • Cell Separation
  • Cells, Cultured
  • Culture Media
  • Flow Cytometry
  • Histocompatibility
  • Humans
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / metabolism
  • Nerve Tissue Proteins / biosynthesis*
  • Receptors, Nerve Growth Factor / biosynthesis*
  • Serum
  • Stromal Cells / cytology*
  • Stromal Cells / metabolism

Substances

  • Antigens, Differentiation
  • Culture Media
  • NGFR protein, human
  • Nerve Tissue Proteins
  • Receptors, Nerve Growth Factor