4.6 Article

LNGFR+THY-1+VCAM-1hi+ Cells Reveal Functionally Distinct Subpopulations in Mesenchymal Stem Cells

期刊

STEM CELL REPORTS
卷 1, 期 2, 页码 152-165

出版社

CELL PRESS
DOI: 10.1016/j.stemcr.2013.06.001

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资金

  1. Medical Research Council, UK
  2. Project for Realization of Regenerative Medicine
  3. Core Institutes for iPS Cell Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
  4. Keio University
  5. Global Century COE program of MEXT
  6. MRC [G0802350] Funding Source: UKRI
  7. Medical Research Council [G0802350] Funding Source: researchfish
  8. Grants-in-Aid for Scientific Research [25463226] Funding Source: KAKEN

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Human mesenchymal stem cells (hMSCs), which conventionally are isolated based on their adherence to plastic, are heterogeneous and have poor growth and differentiation, limiting our ability to investigate their intrinsic characteristics. We report an improved prospective clonal isolation technique and reveal that the combination of three cell-surface markers (LNGFR, THY-1, and VCAM-1) allows for the selection of highly enriched clonogenic cells (one out of three isolated cells). Clonal characterization of LNGFR(+)THY-1(+) cells demonstrated cellular heterogeneity among the clones. Rapidly expanding clones (RECs) exhibited robust multilineage differentiation and self-renewal potency, whereas the other clones tended to acquire cellular senescence via P16INK4a and exhibited frequent genomic errors. Furthermore, RECs exhibited unique expression of VCAM-1 and higher cellular motility compared with the other clones. The combination marker LNGFR(+)THY-1(+)VCAM-1(hi+) (LTV) can be used selectively to isolate the most potent and genetically stable MSCs.

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