Cell cycle activation in thyroid hormone-induced apoptosis and stem cell development during Xenopus intestinal metamorphosis

被引:0
作者
Tanizaki, Yuta [1 ]
Shibata, Yuki [1 ]
Na, Wonho [1 ]
Shi, Yun-Bo [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Huma, Sect Mol Morphogenesis, NIH, Bethesda, MD 20892 USA
基金
日本学术振兴会;
关键词
programmed cell death; metamorphosis; Xenopus laevis; Xenopus tropicalis; postembryonic development; intestine; thyroid hormone receptor; stem cell; ADULT EPITHELIAL DEVELOPMENT; TARGETED GENE DISRUPTION; RECEPTOR-ALPHA; C-MYC; SONIC HEDGEHOG; AMPHIBIAN METAMORPHOSIS; CONNECTIVE-TISSUE; SIGNALING PATHWAY; DUAL FUNCTIONS; TR-ALPHA;
D O I
10.3389/fendo.2023.1184013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Amphibian metamorphosis resembles mammalian postembryonic development, a period around birth when many organs mature into their adult forms and when plasma thyroid hormone (T3) concentration peaks. T3 plays a causative role for amphibian metamorphosis. This and its independence from maternal influence make metamorphosis of amphibians, particularly anurans such as pseudo-tetraploid Xenopus laevis and its highly related diploid species Xenopus tropicalis, an excellent model to investigate how T3 regulates adult organ development. Studies on intestinal remodeling, a process that involves degeneration of larval epithelium via apoptosis and de novo formation of adult stem cells followed by their proliferation and differentiation to form the adult epithelium, have revealed important molecular insights on T3 regulation of cell fate during development. Here, we review some evidence suggesting that T3-induced activation of cell cycle program is important for T3-induced larval epithelial cell death and de novo formation of adult intestinal stem cells.
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页数:8
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