Potential Effect of CD271 on Human Mesenchymal Stromal Cell Proliferation and Differentiation

Int J Mol Sci. 2015 Jul 9;16(7):15609-24. doi: 10.3390/ijms160715609.

Abstract

The Low-Affinity Nerve Growth Factor Receptor (LNGFR), also known as CD271, is a member of the tumor necrosis factor receptor superfamily. The CD271 cell surface marker defines a subset of multipotential mesenchymal stromal cells and may be used to isolate and enrich cells derived from bone marrow aspirate. In this study, we compare the proliferative and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells. Mesenchymal stromal cells were isolated from bone marrow aspirate and adipose tissue by plastic adherence and positive selection. The proliferation and differentiation potentials of CD271+ and CD271- mesenchymal stromal cells were assessed by inducing osteogenic, adipogenic and chondrogenic in vitro differentiation. Compared to CD271+, CD271- mesenchymal stromal cells showed a lower proliferation rate and a decreased ability to give rise to osteocytes, adipocytes and chondrocytes. Furthermore, we observed that CD271+ mesenchymal stromal cells isolated from adipose tissue displayed a higher efficiency of proliferation and trilineage differentiation compared to CD271+ mesenchymal stromal cells isolated from bone marrow samples, although the CD271 expression levels were comparable. In conclusion, these data show that both the presence of CD271 antigen and the source of mesenchymal stromal cells represent important factors in determining the ability of the cells to proliferate and differentiate.

Keywords: CD271; adipogenic differentiation; adipose tissue; bone marrow; chondrogenic differentiation; mesenchymal stromal cells; osteogenic differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipogenesis
  • Aged
  • Bone Marrow Cells / cytology
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Chondrogenesis
  • Female
  • Humans
  • Immunohistochemistry
  • Male
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*
  • Middle Aged
  • Nerve Tissue Proteins / metabolism*
  • Osteogenesis
  • Phenotype
  • Receptors, Nerve Growth Factor / metabolism*

Substances

  • NGFR protein, human
  • Nerve Tissue Proteins
  • Receptors, Nerve Growth Factor