Xu Yongsheng, Guo Rui, Huang Tao, Guo Chunming
Center for Life Sciences, School of Life Sciences, Yunnan University, Kunming, 650500, China.
Cell Death Discov. 2024 May 2;10(1):209. doi: 10.1038/s41420-024-01977-6.
Hematopoiesis ensures tissue oxygenation, and remodeling as well as immune protection in vertebrates. During embryogenesis, hemangioblasts are the source of all blood cells. Gata1a and pu.1 are co-expressed in hemangioblasts before hemangioblasts are differentiated into blood cells. However, the genes that determine the differentiation of hemangioblasts into myeloid or erythroid cell lineages have not been fully uncovered. Here we showed that miRNA-7145, a miRNA with previously unknown function, was enriched in erythrocytes at the definitive wave, but not expressed in myeloid cells. Overexpression and loss-of-function analysis of miRNA-7145 revealed that miRNA-7145 functions as a strong inhibitor for myeloid progenitor cell differentiation while driving erythropoiesis during the primitive wave. Furthermore, we confirmed that cuedc2 is one of miRNA-7145 targeted-genes. Overexpression or knock-down of cuedc2 partially rescues the phenotype caused by miRNA-7145 overexpression or loss-of-function. As well, overexpression and loss-of-function analysis of cuedc2 showed that cuedc2 is required for myelopoiesis at the expense of erythropoiesis. Finally, we found that overexpression of zebrafish cuedc2 in 293 T cell inhibits the JAK1/STAT3 signaling pathway. Collectively, our results uncover a previously unknown miRNA-7145-cuedc2 axis, which regulate hematopoiesis through inhibiting the JAK1/STAT3 signaling pathway.
造血作用确保了脊椎动物的组织氧合、重塑以及免疫保护。在胚胎发育过程中,成血管细胞是所有血细胞的来源。在成血管细胞分化为血细胞之前,Gata1a和pu.1在成血管细胞中共同表达。然而,决定成血管细胞分化为髓系或红系细胞谱系的基因尚未完全被揭示。在这里,我们表明miRNA - 7145,一种功能此前未知的miRNA,在定型期的红细胞中富集,但在髓系细胞中不表达。对miRNA - 7145的过表达和功能缺失分析表明,miRNA - 7145在原始期驱动红细胞生成的同时,作为髓系祖细胞分化的强力抑制剂发挥作用。此外,我们证实cuedc2是miRNA - 7145的靶基因之一。cuedc2的过表达或敲低部分挽救了由miRNA - 7145过表达或功能缺失引起的表型。同样,对cuedc2的过表达和功能缺失分析表明,cuedc2是髓系造血所必需的,代价是红细胞生成。最后,我们发现斑马鱼cuedc2在293 T细胞中的过表达抑制了JAK1/STAT3信号通路。总的来说,我们的结果揭示了一个此前未知的miRNA - 7145 - cuedc2轴,其通过抑制JAK1/STAT3信号通路来调节造血作用。