A comprehensive characterization study of human bone marrow mscs with an emphasis on molecular and ultrastructural properties

J Cell Physiol. 2011 May;226(5):1367-82. doi: 10.1002/jcp.22468.

Abstract

Human bone marrow-derived mesenchymal stem cells (hBM-MSCs) continue to draw attention of researchers in the fields of basic science and medicine due to their indispensible regenerative, reparative, angiogenic, anti-apoptotic, and immunosuppressive properties, all of which collectively point out their enormous therapeutic potential. There is still, however, a need for further investigation of their characteristics to broaden their field of use and learn much more about how to control their fate and improve their therapeutic effectiveness. hBM-MSCs were extensively characterized in terms of their growth characteristics, genetic stability, and differentiation capability to the mesodermal and ectodermal cell lineages; a special emphasis was given to their phenotypic and ultrastructural properties. Expression of embryonic stem cell markers Oct4, Rex-1, FoxD-3, Sox2, and Nanog was shown with real-time PCR. Transmission electron microscopy revealed the ultrastructural characteristics of hBM-MSCs; they had pale, irregularly shaped and large euchromatic nuclei, and two distinct areas in their cytoplasm: an intensely stained inner zone rich in mitochondria and rough endoplasmic reticulum (rER) with dilated cisternae and a relatively peripheral zone poor in organelles. hBM-MSCs expressed adipogenic (adipophilin and PPARγ), myogenic (desmin, myogenin, α-SMA), neurogenic (γ-enolase, MAP2a,b, c-fos, nestin, NF-H, NF-L, GFAP, β3-tubulin), osteogenic (osteonectin, osteocalcin, osteopontin, Runx-2, type I collagen), and chondrogenic (type II collagen, SOX9) markers either at RNA or protein level even under basal conditions, without any stimulation towards differentiation. The differentiation potential of hBM-MSCs to adipogenic, osteogenic, and neurogenic lineages was shown by using the relevant differentiation factors.

MeSH terms

  • Adipogenesis / genetics
  • Biomarkers / metabolism
  • Bone Marrow Cells* / metabolism
  • Bone Marrow Cells* / ultrastructure
  • Cell Cycle / genetics
  • Cell Differentiation* / genetics
  • Cell Proliferation
  • Cell Shape
  • Cells, Cultured
  • Cellular Senescence / genetics
  • Child
  • Child, Preschool
  • Chondrogenesis / genetics
  • Flow Cytometry
  • Forkhead Transcription Factors / genetics
  • Gene Expression Profiling / methods
  • Gene Expression Regulation
  • Genomic Instability*
  • Genotype
  • Homeodomain Proteins / genetics
  • Humans
  • Immunohistochemistry
  • Kruppel-Like Transcription Factors / genetics
  • Mesenchymal Stem Cells* / metabolism
  • Mesenchymal Stem Cells* / ultrastructure
  • Microscopy, Electron, Transmission
  • Muscle Development / genetics
  • Nanog Homeobox Protein
  • Neurogenesis / genetics
  • Octamer Transcription Factor-3 / genetics
  • Osteogenesis / genetics
  • Phenotype
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • SOXB1 Transcription Factors / genetics
  • Telomerase / metabolism
  • Time Factors

Substances

  • Biomarkers
  • FOXD3 protein, human
  • Forkhead Transcription Factors
  • Homeodomain Proteins
  • Kruppel-Like Transcription Factors
  • NANOG protein, human
  • Nanog Homeobox Protein
  • Octamer Transcription Factor-3
  • POU5F1 protein, human
  • RNA, Messenger
  • SOX2 protein, human
  • SOXB1 Transcription Factors
  • ZFP42 protein, human
  • Telomerase