Phenotypical and functional characteristics of mesenchymal stem cells from bone marrow: comparison of culture using different media supplemented with human platelet lysate or fetal bovine serum

Stem Cell Res Ther. 2012 Feb 14;3(1):6. doi: 10.1186/scrt97.


Introduction: Mesenchymal stem cells (MSCs) are multipotent cells able to differentiate into several mesenchymal lineages, classically derived from bone marrow (BM) but potentially from umbilical cord blood (UCB). Although they are becoming a good tool for regenerative medicine, they usually need to be expanded in fetal bovine serum (FBS)-supplemented media. Human platelet lysate (HPL) has recently been proposed as substitute for safety reasons, but it is not yet clear how this supplement influences the properties of expanded MSCs.

Methods: In the present study, we compared the effect of various media combining autologous HPL with or without FBS on phenotypic, proliferative and functional (differentiation, cytokine secretion profile) characteristics of human BM-derived MSCs.

Results: Despite less expression of adipogenic and osteogenic markers, MSCs cultured in HPL-supplemented media fully differentiated along osteoblastic, adipogenic, chondrogenic and vascular smooth muscle lineages. The analyses of particular specific proteins expressed during osteogenic differentiation (calcium-sensing receptor (CaSR) and parathormone receptor (PTHR)) showed their decrease at D0 before any induction for MSC cultured with HPL mostly at high percentage (10%HPL). The cytokine dosage showed a clear increase of proliferation capacity and interleukin (IL)-6 and IL-8 secretion.

Conclusions: This study shows that MSCs can be expanded in media supplemented with HPL that can totally replace FBS. HPL-supplemented media not only preserves their phenotype as well as their differentiation capacity, but also shortens culture time by increasing their growth rate.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Blood Platelets / cytology*
  • Bone Marrow Cells / cytology
  • Cattle
  • Cell Differentiation / drug effects
  • Cell Extracts / pharmacology*
  • Cells, Cultured
  • Culture Media / pharmacology
  • Humans
  • Interleukin-6 / metabolism
  • Interleukin-8 / metabolism
  • Mesenchymal Stem Cells / cytology*
  • Mesenchymal Stem Cells / drug effects
  • Mesenchymal Stem Cells / metabolism
  • Phenotype
  • Receptors, Calcium-Sensing / metabolism
  • Receptors, Parathyroid Hormone / metabolism


  • Cell Extracts
  • Culture Media
  • Interleukin-6
  • Interleukin-8
  • Receptors, Calcium-Sensing
  • Receptors, Parathyroid Hormone