4.2 Review

Unexpected role of inflammatory signaling in hematopoietic stem cell development: its role beyond inflammation

Journal

CURRENT OPINION IN HEMATOLOGY
Volume 23, Issue 1, Pages 18-22

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MOH.0000000000000197

Keywords

hematopoietic stem cell; hemogenic endothelium; inflammatory signaling; Toll-like receptor 4 nuclear factor kappa-light chain enhancer of activated B

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Funding

  1. National Basic Research Program of China [2010CB945302, 2011CB943904]
  2. National Natural Science Foundation of China [31271570, 31425016]
  3. Strategic Priority Research Program of the Chinese Academy of Sciences [XDA01010110]

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Purpose of review Inflammatory signaling under pathological conditions like infection and inflammation has been extensively studied. Whether inflammatory signaling plays a role in physiology and development remains elusive. The review summarizes recent advances in inflammatory signaling with particular focus on how distinct inflammatory signaling regulates hematopoietic stem cell (HSC) development. Understanding the underlying mechanism of inflammatory signaling on HSC development may help to generate and/or expand a large number of functional HSCs for clinical application. Recent findings Like the hematopoietic progenitors, HSCs can be the first responders to infection. An unexpected observation is that genes involved in innate immunity and inflammatory signaling are enriched in emerging HSCs and their niche during embryogenesis. Thus, inflammatory signaling may also play a role in HSC development in the absence of infection and inflammation. Summary Inflammatory signaling is not only an important regulator of HSCs in response to infection, but also plays a previously unrecognized role in HSC development in the absence of infection and inflammation. The baseline inflammatory signaling can be activated to promote HSC development in cell autonomous and noncell autonomous manners. However, direct response of HSCs to inflammatory stimuli is not always advantageous and excessive chronic signaling can have negative effects on HSC regulation and function.

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