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Efficient megakaryopoiesis and platelet production require phospholipid remodeling and PUFA uptake through CD36

Maria N. Barrachina, Gerard Pernes, Isabelle C. Becker, Isabelle Allaeys, Thomas I. Hirsch, Dafna J. Groeneveld, Abdullah O. Khan,Daniela Freire, Karen Guo, Estelle Carminita, Pooranee K. Morgan, Thomas J. C. Collins, Natalie A. Mellett, Zimu Wei, Ibrahim Almazni, Joseph E. Italiano, James Luyendyk, Peter J. Meikle, Mark Puder, Neil V. Morgan, Eric Boilard, Andrew J. Murphy, Kellie R. Machlus

Nature Cardiovascular Research(2023)

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摘要
Lipids contribute to hematopoiesis and membrane properties and dynamics; however, little is known about the role of lipids in megakaryopoiesis. Here we show that megakaryocyte progenitors, megakaryocytes and platelets present a unique lipidome progressively enriched in polyunsaturated fatty acid (PUFA)-containing phospholipids. In vitro, inhibition of both exogenous fatty acid functionalization and uptake as well as de novo lipogenesis impaired megakaryocyte differentiation and proplatelet production. In vivo, mice on a high saturated fatty acid diet had significantly lower platelet counts, which was prevented by eating a PUFA-enriched diet. Fatty acid uptake was largely dependent on CD36, and its deletion in mice resulted in low platelets. Moreover, patients with a CD36 loss-of-function mutation exhibited thrombocytopenia and increased bleeding. Our results suggest that fatty acid uptake and regulation is essential for megakaryocyte maturation and platelet production and that changes in dietary fatty acids may be a viable target to modulate platelet counts. Barrachina et al. present an extensive lipidomic analysis at different stages of thrombopoiesis and, through in vitro and in vivo experiments, demonstrate that fatty acid uptake, largely dependent on the scavenger receptor CD36, and its regulation are essential for megakaryocyte maturation and platelet production.
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