Stem Cell Reports · 2014 · 107 citations · 16 references
Life SciencesCell BiologyHematologyCell DifferentiationStem Cell BiologyStem Cell TransplantationBone Marrow MicroenvironmentBone Marrow PhysiologyHematopoietic DifferentiationHematopoietic Stem Cell BiologyHematopoietic Stem CellsMesenchymal DifferentiationBone Marrow Mesenchymal Stem CellsBone Marrow-derived Mesenchymal Stromal CellsEx Vivo Cell ExpansionEx Vivo Stem Cell ExpansionHematopoietic MicroenvironmentMesenchymal Stromal Cell ExpansionNegative SelectionNegative Selection Markers
Human bone marrow (BM) contains a rare population of nonhematopoietic mesenchymal stromal cells (MSCs), which are of central importance for the hematopoietic microenvironment. However, the precise phenotypic definition of these cells in adult BM has not yet been reported. In this study, we show that low/negative expression of CD140a (PDGFR-α) on lin(-)/CD45(-)/CD271(+) BM cells identified a cell population with very high MSC activity, measured as fibroblastic colony-forming unit frequency and typical in vitro and in vivo stroma formation and differentiation capacities. Furthermore, these cells exhibited high levels of genes associated with mesenchymal lineages and HSC supportive function. Moreover, lin(-)/CD45(-)/CD271(+)/CD140a(low/-) cells effectively mediated the ex vivo expansion of transplantable CD34(+) hematopoietic stem cells. Taken together, these data indicate that CD140a is a key negative selection marker for adult human BM-MSCs, which enables to prospectively isolate a close to pure population of candidate human adult stroma stem/progenitor cells with potent hematopoiesis-supporting capacity.
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