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基于年龄和饮食,脂肪酸氧化对造血干细胞的不同影响。

Different effects of fatty acid oxidation on hematopoietic stem cells based on age and diet.

作者信息

Merchant Salma, Paul Animesh, Reyes Amanda, Cassidy Daniel, Leach Ashley, Kim Dohun, Muh Sarah, Grabowski Gerik, Hoxhaj Gerta, Zhao Zhiyu, Morrison Sean J

机构信息

Children's Research Institute and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Children's Research Institute and the Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA; Howard Hughes Medical Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

出版信息

Cell Stem Cell. 2025 Feb 6;32(2):263-275.e5. doi: 10.1016/j.stem.2024.11.014. Epub 2024 Dec 20.

Abstract

Fatty acid oxidation is of uncertain importance in most stem cells. We show by C-palmitate tracing and metabolomic analysis that hematopoietic stem/progenitor cells (HSPCs) engage in long-chain fatty acid oxidation that depends upon carnitine palmitoyltransferase 1a (CPT1a) and hydroxyacyl-CoA dehydrogenase (HADHA) enzymes. CPT1a or HADHA deficiency had little or no effect on HSPCs or hematopoiesis in young adult mice. Young HSPCs had the plasticity to oxidize other substrates, including glutamine, and compensated for loss of fatty acid oxidation by decreasing pyruvate dehydrogenase phosphorylation, which should increase function. This metabolic plasticity declined as mice aged, when CPT1a or HADHA deficiency altered hematopoiesis and impaired hematopoietic stem cell (HSC) function upon serial transplantation. A high-fat diet increased fatty acid oxidation and reduced HSC function. This was rescued by CPT1a or HADHA deficiency, demonstrating that increased fatty acid oxidation can undermine HSC function. Long-chain fatty acid oxidation is thus dispensable in young HSCs but necessary during aging and deleterious with a high-fat diet.

摘要

在大多数干细胞中,脂肪酸氧化的重要性尚不确定。我们通过碳 - 棕榈酸追踪和代谢组学分析表明,造血干/祖细胞(HSPCs)参与长链脂肪酸氧化,这依赖于肉碱棕榈酰转移酶1a(CPT1a)和羟酰基辅酶A脱氢酶(HADHA)。CPT1a或HADHA缺乏对年轻成年小鼠的HSPCs或造血作用几乎没有影响。年轻的HSPCs具有氧化其他底物(包括谷氨酰胺)的可塑性,并通过减少丙酮酸脱氢酶磷酸化来补偿脂肪酸氧化的损失,这应该会增加其功能。随着小鼠年龄增长,这种代谢可塑性下降,此时CPT

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