Acly缺乏通过乙酰辅酶A和代谢-表观遗传串扰促进骨髓生成。

Dalton L Greenwood, Haley E Ramsey, Phuong T T Nguyen, Andrew R Patterson, Kelsey Voss, Jackie E Bader, Ayaka Sugiura, Zachary A Bacigalupa, Samuel Schaefer, Xiang Ye, Debolanle O Dahunsi, Matthew Z Madden, Kathryn E Wellen, Michael R Savona, P Brent Ferrell, Jeffrey C Rathmell
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引用次数: 0

摘要

造血整合了细胞因子信号,代谢和表观遗传修饰来调节血细胞的产生。这些过程是相互联系的,因为代谢物为表观遗传标记提供了必要的底物。在这项研究中,我们证明ATP柠檬酸裂解酶(Acly),代谢柠檬酸生成胞浆乙酰辅酶a,具有临床意义,可以调节染色质可及性以限制髓细胞分化。通过小分子抑制或基因缺失来检测Acly在小鼠造血中的作用,这些抑制或基因缺失来自小家鼠的造血干细胞和祖细胞中富含c- kit。治疗增加了表达髓系整合素CD11b和其他髓系分化标志物的细胞群的丰度。当进行单细胞RNA测序时,我们发现Acly抑制剂处理的造血干细胞和祖细胞对巨噬细胞表现出更大的基因表达特征和这些群体的富集。同样,转座酶可及染色质测序的单细胞试验显示,与髓细胞分化相关的基因(包括CD11b、CD11c和IRF8)的染色质可及性增加。在机制上,Acly缺乏改变了染色质可及性和多种C/EBP家族转录因子的表达,这些转录因子调节髓细胞分化和细胞代谢,Cebpe增加,Cebpa和Cebpb减少。这种影响伴随着线粒体代谢的改变,线粒体极化减少,线粒体含量和活性氧的产生增加。骨髓分化的倾向是由于乙酰辅酶a的产生不足,因为外源性醋酸盐支持替代代偿途径产生乙酰辅酶a逆转了这种表型。因此,Acly抑制可以通过剥夺乙酰辅酶a和改变组蛋白乙酰组来促进髓细胞形成,从而调节C/EBP转录因子家族活性,促进髓细胞分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Acly Deficiency Enhances Myelopoiesis through Acetyl Coenzyme A and Metabolic-Epigenetic Cross-Talk.

Hematopoiesis integrates cytokine signaling, metabolism, and epigenetic modifications to regulate blood cell generation. These processes are linked, as metabolites provide essential substrates for epigenetic marks. In this study, we demonstrate that ATP citrate lyase (Acly), which metabolizes citrate to generate cytosolic acetyl-CoA and is of clinical interest, can regulate chromatin accessibility to limit myeloid differentiation. Acly was tested for a role in murine hematopoiesis by small-molecule inhibition or genetic deletion in lineage-depleted, c-Kit-enriched hematopoietic stem and progenitor cells from Mus musculus. Treatments increased the abundance of cell populations that expressed the myeloid integrin CD11b and other markers of myeloid differentiation. When single-cell RNA sequencing was performed, we found that Acly inhibitor-treated hematopoietic stem and progenitor cells exhibited greater gene expression signatures for macrophages and enrichment of these populations. Similarly, the single-cell assay for transposase-accessible chromatin sequencing showed increased chromatin accessibility at genes associated with myeloid differentiation, including CD11b, CD11c, and IRF8. Mechanistically, Acly deficiency altered chromatin accessibility and expression of multiple C/EBP family transcription factors known to regulate myeloid differentiation and cell metabolism, with increased Cebpe and decreased Cebpa and Cebpb. This effect of Acly deficiency was accompanied by altered mitochondrial metabolism with decreased mitochondrial polarization but increased mitochondrial content and production of reactive oxygen species. The bias to myeloid differentiation appeared due to insufficient generation of acetyl-CoA, as exogenous acetate to support alternate compensatory pathways to produce acetyl-CoA reversed this phenotype. Acly inhibition thus can promote myelopoiesis through deprivation of acetyl-CoA and altered histone acetylome to regulate C/EBP transcription factor family activity for myeloid differentiation.

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