Stage-specific regulation by autophagy-related transcription factors drives hematopoietic stem cell formation.

IF 14.3
Autophagy Pub Date : 2025-10-01 Epub Date: 2025-08-28 DOI:10.1080/15548627.2025.2551671
Jia Chen, Jiayi Zheng, Xiaoya Chen, Gangjue Tang, Yan Huang
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Abstract

Macroautophagy/autophagy critically regulates hematopoietic stem cell (HSC) development and differentiation, yet the upstream transcriptional mechanisms governing autophagy during dynamic developmental processes remain poorly characterized. Here, we combined single-cell RNA sequencing (scRNA-seq) with metaTF to dissect six consecutive stages of murine HSC development, spanning the aorta-gonad-mesonephros (AGM) region at embryonic day (E) 10.5, the fetal liver at E12.5/E14.5, and adult bone marrow. Beyond transcript abundance alone, we found that the activity of autophagy-related transcription factors (TFs) more robustly characterized cell-type specificity, particularly distinguishing T1 and T2 pre-HSCs, and identified 32 cell-type-specific autophagy-related TFs. Stage-specific autophagy-related TF-target gene networks constructed for T1 and T2 revealed functional partitioning of the pre-HSC stage: an early T1 phase characterized by elevated autophagy activity, and a later T2 phase primarily involved in proliferation and maturation. These findings highlight the temporal regulation exerted by autophagy-related TFs during embryonic hematopoiesis and underscore the importance of autophagy in stem cell fate decision.Abbreviations: HSC: hematopoietic stem cell; TF: transcription factor.

自噬相关转录因子的阶段特异性调控驱动造血干细胞的形成。
巨噬/自噬对造血干细胞(HSC)的发育和分化起着至关重要的调节作用,然而,在动态发育过程中调控自噬的上游转录机制仍不清楚。在这里,我们结合单细胞RNA测序(scRNA-seq)和metaTF来解剖小鼠HSC发育的六个连续阶段,包括胚胎日(E) 10.5时的主动脉-性腺-中肾(AGM)区域,E12.5/E14.5时的胎儿肝脏和成人骨髓。除了转录丰度之外,我们发现自噬相关转录因子(TFs)的活性更有力地表征了细胞类型特异性,特别是区分T1和T2前hsc,并鉴定了32种细胞类型特异性自噬相关tf。针对T1和T2构建的阶段特异性自噬相关tf靶基因网络揭示了hsc前阶段的功能划分:早期T1阶段以自噬活性升高为特征,晚期T2阶段主要参与增殖和成熟。这些发现强调了自噬相关tf在胚胎造血过程中发挥的时间调节作用,并强调了自噬在干细胞命运决定中的重要性。缩写:HSC:造血干细胞;TF:转录因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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