Key Laboratory of Functional Proteomics of Guangdong Province, Department of Developmental Biology, School of Basic Medical Sciences, Southern Medical University, Guangzhou, China.
Institute of Hematology, School of Medicine, Jinan University, Guangzhou, China.
Nat Commun. 2024 Mar 15;15(1):2255. doi: 10.1038/s41467-024-46453-y.
An understanding of the mechanisms regulating embryonic hematopoietic stem cell (HSC) development would facilitate their regeneration. The aorta-gonad-mesonephros region is the site for HSC production from hemogenic endothelial cells (HEC). While several distinct regulators are involved in this process, it is not yet known whether macroautophagy (autophagy) plays a role in hematopoiesis in the pre-liver stage. Here, we show that different states of autophagy exist in hematopoietic precursors and correlate with hematopoietic potential based on the LC3-RFP-EGFP mouse model. Deficiency of autophagy-related gene 5 (Atg5) specifically in endothelial cells disrupts endothelial to hematopoietic transition (EHT), by blocking the autophagic process. Using combined approaches, including single-cell RNA-sequencing (scRNA-seq), we have confirmed that Atg5 deletion interrupts developmental temporal order of EHT to further affect the pre-HSC I maturation, and that autophagy influences hemogenic potential of HEC and the formation of pre-HSC I likely via the nucleolin pathway. These findings demonstrate a role for autophagy in the formation/maturation of hematopoietic precursors.
理解调节胚胎造血干细胞(HSC)发育的机制将有助于它们的再生。主动脉-性腺-中肾区是从造血内皮细胞(HEC)产生 HSC 的部位。虽然有几个不同的调节因子参与这个过程,但目前尚不清楚巨自噬(自噬)是否在肝前阶段的造血中发挥作用。在这里,我们使用 LC3-RFP-EGFP 小鼠模型显示,自噬在造血前体中存在不同的状态,并根据造血潜力与之相关。特异性在血管内皮细胞中缺失自噬相关基因 5(Atg5)会通过阻断自噬过程破坏血管内皮向造血的转变(EHT)。通过结合单细胞 RNA 测序(scRNA-seq)等多种方法,我们已经证实 Atg5 的缺失中断了 EHT 的发育时间顺序,从而进一步影响了前 HSC I 的成熟,并且自噬可能通过核仁素途径影响 HEC 的造血潜能和前 HSC I 的形成。这些发现表明自噬在造血前体的形成/成熟中起作用。