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Inflammation-Induced Emergency Megakaryopoiesis Driven by Hematopoietic Stem Cell-like Megakaryocyte Progenitors

机译:由造血干细胞样巨核细胞祖细胞驱动的炎症诱导的紧急巨核细胞生成

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摘要

Infections are associated with extensive platelet consumption, representing a high risk for health. However, the mechanism coordinating the rapid regeneration of the platelet pool during such stress conditions remains unclear. Here, we report that the phenotypic hematopoietic stem cell (HSC) compartment contains stem-like megakaryocyte-committed progenitors (SL-MkPs), a cell population that shares many features with multipotent HSCs and serves as a lineage-restricted emergency pool for inflammatory insults. During homeostasis, SL-MkPs are maintained in a primed but quiescent state, thus contributing little to steady-state megakaryopoiesis. Even though lineage-specific megakaryocyte transcripts are expressed, protein synthesis is suppressed. In response to acute inflammation, SL-MkPs become activated, resulting in megakaryocyte protein production from pre-existing transcripts and a maturation of SL-MkPs and other megakaryocyte progenitors. This results in an efficient replenishment of platelets that are lost during inflammatory insult. Thus, our study reveals an emergency machinery that counteracts life-threatening platelet depletions during acute inflammation.
机译:感染与大量食用血小板有关,对健康构成高风险。然而,在这样的应激条件下协调血小板池快速再生的机制仍然不清楚。在这里,我们报道表型造血干细胞(HSC)隔室包含干样巨核细胞定型祖细胞(SL-MkPs),该细胞群与多能HSC具有许多功能,并且是炎性损伤的谱系限制应急池。在稳态过程中,SL-MkPs保持处于启动状态但处于静止状态,因此对稳态巨核细胞的贡献很小。即使表达了谱系特异性的巨核细胞转录本,蛋白质合成也受到抑制。响应急性炎症,SL-MkPs被激活,导致现有转录本产生巨核细胞蛋白质,并使SL-MkPs和其他巨核细胞祖细胞成熟。这导致在炎症损伤期间丢失的血小板的有效补充。因此,我们的研究揭示了一种应急机制,可以抵消急性炎症期间危及生命的血小板消耗。

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