Institut Pasteur, Department of Developmental and Stem Cell Biology, 75015 Paris, France.
CNRS, UMR3738, 75015 Paris, France.
Development. 2022 Sep 15;149(18). doi: 10.1242/dev.200835. Epub 2022 Sep 16.
Trim33 (Tif1γ) is a transcriptional regulator that is notably involved in several aspects of hematopoiesis. It is essential for the production of erythrocytes in zebrafish, and for the proper functioning and aging of hematopoietic stem and progenitor cells (HSPCs) in mice. Here, we have found that, in zebrafish development, Trim33 is essential cell-autonomously for the lifespan of the yolk sac-derived primitive macrophages, as well as for the initial production of definitive (HSPC-derived) macrophages in the first niche of definitive hematopoiesis, the caudal hematopoietic tissue. Moreover, Trim33 deficiency leads to an excess production of definitive neutrophils and thrombocytes. Our data indicate that Trim33 radically conditions the differentiation output of aorta-derived HSPCs in all four erythro-myeloid cell types, in a niche-specific manner.
Trim33(Tif1γ)是一种转录调节因子,它显著参与了造血的多个方面。它对于斑马鱼红细胞的生成以及小鼠造血干细胞和祖细胞(HSPC)的正常功能和衰老至关重要。在这里,我们发现,在斑马鱼发育过程中,Trim33 自主地对卵黄囊衍生的原始巨噬细胞的寿命以及在确定性造血的第一个龛位(尾造血组织)中最初产生的确定性(HSPC 衍生)巨噬细胞的产生是必需的。此外,Trim33 缺乏会导致确定性中性粒细胞和血小板的过度产生。我们的数据表明,Trim33 以龛位特异性的方式从根本上调节了源自主动脉的 HSPC 在所有四种红髓细胞类型中的分化产物。