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高效的巨核细胞生成和血小板生成需要通过CD36进行磷脂重塑和多不饱和脂肪酸摄取。

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

作者信息

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

机构信息

Vascular Biology Program, Boston Children's Hospital, Boston, MA, 02115 USA.

Harvard Medical School, Department of Surgery, Boston Children's Hospital, Boston, MA, 02115 USA.

出版信息

bioRxiv. 2023 Feb 12:2023.02.12.527706. doi: 10.1101/2023.02.12.527706.

DOI:10.1101/2023.02.12.527706
PMID:36798332
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9934665/
Abstract

Lipids contribute to hematopoiesis and membrane properties and dynamics, however, little is known about the role of lipids in megakaryopoiesis. Here, a lipidomic analysis of megakaryocyte progenitors, megakaryocytes, and platelets revealed a unique lipidome progressively enriched in polyunsaturated fatty acid (PUFA)-containing phospholipids. In vitro, inhibition of both exogenous fatty acid functionalization and uptake and 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 thrombocytopenia. 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 novel and viable target to modulate platelet counts.

摘要

脂质有助于造血以及细胞膜的特性和动态变化,然而,脂质在巨核细胞生成中的作用却鲜为人知。在此,对巨核细胞祖细胞、巨核细胞和血小板进行的脂质组分析揭示了一种独特的脂质组,其在含多不饱和脂肪酸(PUFA)的磷脂中逐渐富集。在体外,抑制外源性脂肪酸功能化、摄取以及从头脂肪生成会损害巨核细胞分化和前血小板生成。在体内,食用高饱和脂肪酸饮食的小鼠血小板计数显著降低,而食用富含PUFA的饮食可预防这一情况。脂肪酸摄取在很大程度上依赖于CD36,在小鼠中删除CD36会导致血小板减少。此外,具有CD36功能丧失突变的患者表现出血小板减少和出血增加。我们的结果表明,脂肪酸摄取和调节对于巨核细胞成熟和血小板生成至关重要,并且饮食脂肪酸的变化可能是调节血小板计数的一个新的可行靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/061546c1186a/nihpp-2023.02.12.527706v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/20ee890f4086/nihpp-2023.02.12.527706v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/f6108625f936/nihpp-2023.02.12.527706v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/aa1cc5eda811/nihpp-2023.02.12.527706v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/55d82e3e948a/nihpp-2023.02.12.527706v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/05c609673cb1/nihpp-2023.02.12.527706v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/061546c1186a/nihpp-2023.02.12.527706v1-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/20ee890f4086/nihpp-2023.02.12.527706v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/f6108625f936/nihpp-2023.02.12.527706v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/aa1cc5eda811/nihpp-2023.02.12.527706v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/55d82e3e948a/nihpp-2023.02.12.527706v1-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/05c609673cb1/nihpp-2023.02.12.527706v1-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/91d9/9934665/061546c1186a/nihpp-2023.02.12.527706v1-f0006.jpg

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