脂肪细胞
骨髓
造血
CD36
血小板生成素
巨核细胞
内科学
内分泌学
祖细胞
脂肪组织
细胞生物学
化学
串扰
生物
干细胞
受体
医学
物理
光学
作者
Colin Valet,Aurélie Batut,Alicia Vauclard,Alizée Dortignac,Marie Bellio,Bernard Payrastre,Philippe Valet,Sonia Séverin
出处
期刊:Cell Reports
[Cell Press]
日期:2020-07-01
卷期号:32 (1): 107875-107875
被引量:41
标识
DOI:10.1016/j.celrep.2020.107875
摘要
Megakaryocytes (MKs) come from a complex process of hematopoietic progenitor maturation within the bone marrow that gives rise to de novo circulating platelets. Bone marrow microenvironment contains a large number of adipocytes with a still ill-defined role. This study aims to analyze the influence of adipocytes and increased medullar adiposity in megakaryopoiesis. An in vivo increased medullar adiposity in mice caused by high-fat-diet-induced obesity is associated to an enhanced MK maturation and proplatelet formation. In vitro co-culture of adipocytes with bone marrow hematopoietic progenitors shows that delipidation of adipocytes directly supports MK maturation by enhancing polyploidization, amplifying the demarcation membrane system, and accelerating proplatelet formation. This direct crosstalk between adipocytes and MKs occurs through adipocyte fatty acid transfer to MKs involving CD36 to reinforce megakaryocytic maturation. Thus, these findings unveil an influence of adiposity on MK homeostasis based on a dialogue between adipocytes and MKs.
科研通智能强力驱动
Strongly Powered by AbleSci AI