Tam Patrick P L, Khoo Poh-Lynn, Lewis Samara L, Bildsoe Heidi, Wong Nicole, Tsang Tania E, Gad Jacqueline M, Robb Lorraine
Embryology Unit, Children's Medical Research Institute, University of Sydney, Locked bag 23, Wentworthville, New South Wales 2145, Australia.
Development. 2007 Jan;134(2):251-60. doi: 10.1242/dev.02724. Epub 2006 Dec 6.
During mouse gastrulation, endoderm cells of the dorsal foregut are recruited ahead of the ventral foregut and move to the anterior region of the embryo via different routes. Precursors of the anterior-most part of the foregut and those of the mid- and hind-gut are allocated to the endoderm of the mid-streak-stage embryo, whereas the precursors of the rest of the foregut are recruited at later stages of gastrulation. Loss of Mixl1 function results in reduced recruitment of the definitive endoderm, and causes cells in the endoderm to remain stationary during gastrulation. The observation that the endoderm cells are inherently unable to move despite the expansion of the mesoderm in the Mixl1-null mutant suggests that the movement of the endoderm and the mesoderm is driven independently of one another.
在小鼠原肠胚形成过程中,背侧前肠的内胚层细胞比腹侧前肠的内胚层细胞更早被募集,并通过不同途径迁移至胚胎的前部区域。前肠最前端以及中肠和后肠的前体细胞被分配到中胚层期胚胎的内胚层,而前肠其余部分的前体细胞则在原肠胚形成的后期被募集。Mixl1功能的丧失导致定形内胚层的募集减少,并使内胚层细胞在原肠胚形成过程中保持静止。尽管Mixl1基因敲除突变体中中胚层扩张,但内胚层细胞天生无法移动,这一观察结果表明内胚层和中胚层的运动是相互独立驱动的。