Sun Guihong, Fu Liezhen, Wen Luan, Shi Yun-Bo
School of Basic Medical Sciences (G.S.), Wuhan University, Wuhan 430072, People's Republic of China; and Section on Molecular Morphogenesis (L.F., L.W., Y.-B.S.), Program in Cellular Regulation and Metabolism, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892.
Endocrinology. 2014 Dec;155(12):5024-32. doi: 10.1210/en.2014-1316. Epub 2014 Sep 11.
The maturation of the intestine into the adult form involves the formation of adult stem cells in a thyroid hormone (T3)-dependent process in vertebrates. In mammals, this takes place during postembryonic development, a period around birth when the T3 level peaks. Due to the difficulty of manipulating late-stage, uterus-enclosed embryos, very little is known about the development of the adult intestinal stem cells. Interestingly, the remodeling of the intestine during the T3-dependent amphibian metamorphosis mimics the maturation of mammalian intestine. Our earlier microarray studies in Xenopus laevis revealed that the transcription factor SRY (sex-determining region Y)-box 3 (Sox3), well known for its involvement in neural development, was upregulated in the intestinal epithelium during metamorphosis. Here, we show that Sox3 is highly and specifically expressed in the developing adult intestinal progenitor/stem cells. We further show that its induction by T3 is independent of new protein synthesis, suggesting that Sox3 is directly activated by liganded T3 receptor. Thus, T3 activates Sox3 as one of the earliest changes in the epithelium, and Sox3 in turn may facilitate the dedifferentiation of the larval epithelial cells into adult stem cells.
在脊椎动物中,肠道发育为成体形式的过程涉及在甲状腺激素(T3)依赖的过程中形成成体干细胞。在哺乳动物中,这一过程发生在胚胎后期发育阶段,即出生前后T3水平达到峰值的时期。由于难以操作处于晚期、仍在子宫内的胚胎,人们对成体肠道干细胞的发育了解甚少。有趣的是,在T3依赖的两栖类变态发育过程中肠道的重塑过程模拟了哺乳动物肠道的成熟过程。我们早期对非洲爪蟾的微阵列研究表明,以参与神经发育而闻名的转录因子SRY(性别决定区Y)-盒3(Sox3)在变态发育期间的肠道上皮中上调。在此,我们表明Sox3在发育中的成体肠道祖细胞/干细胞中高度且特异性地表达。我们进一步表明,T3对其的诱导独立于新蛋白质的合成,这表明Sox3是由结合配体的T3受体直接激活的。因此,T3作为上皮细胞最早的变化之一激活Sox3,而Sox3反过来可能促进幼虫上皮细胞去分化为成体干细胞。