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Demand-adapted regulation of early hematopoiesis in infection and inflammation

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BLOOD
卷 119, 期 13, 页码 2991-3002

出版社

AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2011-12-380113

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  1. Japanese Society for the Promotion of Science for Research Abroad
  2. Swiss National Science Foundation [310030_131088/1]
  3. Promedica Foundation (Chur, Switzerland)
  4. Marlis Geiser-Lemken Stiftung (Zurich, Switzerland)

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During systemic infection and inflammation, immune effector cells are in high demand and are rapidly consumed at sites of need. Although adaptive immune cells have high proliferative potential, innate immune cells are mostly postmitotic and need to be replenished from bone marrow (BM) hematopoietic stem and progenitor cells. We here review how early hematopoiesis has been shaped to de-liver efficient responses to increased need. On the basis of most recent findings, we develop an integrated view of how cytokines, chemokines, as well as conserved pathogen structures, are sensed, leading to divisional activation, proliferation, differentiation, and migration of hematopoietic stem and progenitor cells, all aimed at efficient contribution to immune responses and rapid reestablishment of hematopoietic homeostasis. We also outline how chronic inflammatory processes might impinge on hematopoiesis, potentially fostering hematopoietic stem cell diseases, and, how clinical benefit is and could be achieved by learning from nature. (Blood. 2012;119(13):2991-3002)

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