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10.1016/j.stemcr.2015.05.003

http://scihub22266oqcxt.onion/10.1016/j.stemcr.2015.05.003
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suck abstract from ncbi


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pmid26028528
      Stem+Cell+Reports 2015 ; 4 (6 ): 995-1003
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  • Bmi-1 Regulates Extensive Erythroid Self-Renewal #MMPMID26028528
  • Kim AR ; Olsen JL ; England SJ ; Huang YS ; Fegan KH ; Delgadillo LF ; McGrath KE ; Kingsley PD ; Waugh RE ; Palis J
  • Stem Cell Reports 2015[Jun]; 4 (6 ): 995-1003 PMID26028528 show ga
  • Red blood cells (RBCs), responsible for oxygen delivery and carbon dioxide exchange, are essential for our well-being. Alternative RBC sources are needed to meet the increased demand for RBC transfusions projected to occur as our population ages. We previously have discovered that erythroblasts derived from the early mouse embryo can self-renew extensively ex vivo for many months. To better understand the mechanisms regulating extensive erythroid self-renewal, global gene expression data sets from self-renewing and differentiating erythroblasts were analyzed and revealed the differential expression of Bmi-1. Bmi-1 overexpression conferred extensive self-renewal capacity upon adult bone-marrow-derived self-renewing erythroblasts, which normally have limited proliferative potential. Importantly, Bmi-1 transduction did not interfere with the ability of extensively self-renewing erythroblasts (ESREs) to terminally mature either in vitro or in vivo. Bmi-1-induced ESREs can serve to generate in vitro models of erythroid-intrinsic disorders and ultimately may serve as a source of cultured RBCs for transfusion therapy.
  • |Animals [MESH]
  • |Cell Proliferation/drug effects [MESH]
  • |Dexamethasone/pharmacology [MESH]
  • |Erythroblasts/*cytology/metabolism/transplantation [MESH]
  • |Erythropoietin/pharmacology [MESH]
  • |Mice [MESH]
  • |Mice, Inbred C57BL [MESH]
  • |Mice, Inbred ICR [MESH]
  • |Mice, Inbred NOD [MESH]
  • |Mice, Knockout [MESH]
  • |Mice, SCID [MESH]
  • |Mice, Transgenic [MESH]
  • |Polycomb Repressive Complex 1/antagonists & inhibitors/genetics/*metabolism [MESH]
  • |Proto-Oncogene Proteins/antagonists & inhibitors/genetics/*metabolism [MESH]
  • |RNA Interference [MESH]
  • |RNA, Small Interfering/metabolism [MESH]
  • |Stem Cell Factor/pharmacology [MESH]


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