Stem Cell Reports (Jul 2018)

TGF-β1 Negatively Regulates the Number and Function of Hematopoietic Stem Cells

  • Xiaofang Wang,
  • Fang Dong,
  • Sen Zhang,
  • Wanzhu Yang,
  • Wenying Yu,
  • Zhao Wang,
  • Shanshan Zhang,
  • Jinhong Wang,
  • Shihui Ma,
  • Peng Wu,
  • Yun Gao,
  • Ji Dong,
  • Fuchou Tang,
  • Tao Cheng,
  • Hideo Ema

Journal volume & issue
Vol. 11, no. 1
pp. 274 – 287

Abstract

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Summary: Transforming growth factor β1 (TGF-β1) plays a role in the maintenance of quiescent hematopoietic stem cells (HSCs) in vivo. We asked whether TGF-β1 controls the cell cycle status of HSCs in vitro to enhance the reconstitution activity. To examine the effect of TGF-β1 on the HSC function, we used an in vitro culture system in which single HSCs divide with the retention of their short- and long-term reconstitution ability. Extensive single-cell analyses showed that, regardless of its concentration, TGF-β1 slowed down the cell cycle progression of HSCs but consequently suppressed their self-renewal potential. Cycling HSCs were not able to go back to quiescence with TGF-β1. This study revealed a negative role of TGF-β1 in the regulation of the HSC number and reconstitution activity. : Dr. Ema and colleagues report in vitro effect of TGF-β1 on single hematopoietic stem cells (HSCs). TGF-β1 slowed down the cell cycle progression of HSCs but consequently suppressed their self-renewal potential. Cycling HSCs were unable to return to quiescence with TGF-β1. This study revealed a negative role of TGF-β1 in the regulation of the HSC number and reconstitution activity. Keywords: hematopoietic stem cells, transforming growth factor β1, cell cycle, quiescence, self-renewal, apoptosis, differentiation, G0 phase