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TGF-β signaling in the control of hematopoietic stem cells

Journal

BLOOD
Volume 125, Issue 23, Pages 3542-3550

Publisher

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2014-12-618090

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Funding

  1. European Commission
  2. Swedish Research Council
  3. Swedish Cancer Society
  4. Swedish Children Cancer Foundation
  5. Lund University Hospital
  6. Tobias Foundation
  7. Royal Academy of Sciences

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Blood is a tissue with high cellular turnover, and its production is a tightly orchestrated process that requires constant replenishment. All mature blood cells are generated from hematopoietic stem cells (HSCs), which are the self-renewing units that sustain lifelong hematopoiesis. HSC behavior, such as self-renewal and quiescence, is regulated by a wide array of factors, including external signaling cues present in the bone marrow. The transforming growth factor-beta (TGF-beta) family of cytokines constitutes a multifunctional signaling circuitry, which regulates pivotal functions related to cell fate and behavior in virtually all tissuesof thebody. In the hematopoietic system, TGF-beta signaling controls a wide spectrum of biological processes, from homeostasis of the immune system to quiescence and self-renewal of HSCs. Here, we review key features and emerging concepts pertaining to TGF-beta and downstream signaling pathways in normal HSC biology, featuring aspects of aging, hematologic disease, and how this circuitry may be exploited for clinical purposes in the future.

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