Visan Ioana, Tan Joanne B, Yuan Julie S, Harper James A, Koch Ute, Guidos Cynthia J
Program in Developmental Biology, Hospital for Sick Children Research Institute, and Department of Immunology, Faculty of Medicine, University of Toronto, Toronto, Ontario M5G 1L7, Canada.
Nat Immunol. 2006 Jun;7(6):634-43. doi: 10.1038/ni1345. Epub 2006 May 14.
Notch1 activation regulates T lineage commitment and early T cell development. Fringe glycosyltransferases alter the sensitivity of Notch receptors to Delta-like versus Jagged Notch ligands, but their functions in T lymphopoiesis have not been defined. Here we show that developmental stage-specific expression of the glycosyltransferase lunatic fringe (Lfng) is required for coordination of the access of T cell progenitors to intrathymic niches that support Notch1-dependent phases of T cell development. Lfng-null progenitors generated few thymocytes in competitive assays, whereas Lfng overexpression converted thymocytes into 'supercompetitors' with enhanced binding of Delta-like ligands and blocked T lymphopoiesis from normal progenitors. We suggest that the ability of Lfng and Notch1 to control progenitor competition for limiting cortical niches is an important mechanism for the homeostatic regulation of thymus size.
Notch1激活调节T细胞谱系定向和早期T细胞发育。边缘糖基转移酶改变Notch受体对Delta样与锯齿状Notch配体的敏感性,但其在T淋巴细胞生成中的功能尚未明确。我们在此表明,糖基转移酶月桂酸边缘蛋白(Lfng)的发育阶段特异性表达对于协调T细胞祖细胞进入支持Notch1依赖性T细胞发育阶段的胸腺微环境是必需的。在竞争性试验中,Lfng基因缺失的祖细胞产生的胸腺细胞很少,而Lfng的过表达将胸腺细胞转化为“超级竞争者”,增强了与Delta样配体的结合,并阻断了正常祖细胞的T淋巴细胞生成。我们认为,Lfng和Notch1控制祖细胞对有限皮质微环境竞争的能力是胸腺大小稳态调节的重要机制。