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甲状腺激素诱导的细胞凋亡和肠变态过程中干细胞发育的细胞周期激活。

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

机构信息

Section on Molecular Morphogenesis, Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD, United States.

出版信息

Front Endocrinol (Lausanne). 2023 May 17;14:1184013. doi: 10.3389/fendo.2023.1184013. eCollection 2023.

Abstract

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 and its highly related diploid species , 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 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 formation of adult intestinal stem cells.

摘要

两栖动物的变态发育类似于哺乳动物的胚胎后发育,这是出生前后的一个时期,在此期间,许多器官成熟为成体形式,血浆甲状腺激素 (T3) 浓度达到峰值。T3 对两栖动物的变态发育起着因果作用。这种作用及其与母体影响的独立性使得两栖动物,特别是类似伪四倍体及其高度相关的二倍体物种的无尾两栖类,成为研究 T3 如何调节成体器官发育的极佳模型。对肠道重塑的研究揭示了 T3 如何调节发育过程中细胞命运的重要分子见解,该过程涉及通过细胞凋亡使幼虫上皮退化,并形成成体干细胞,然后通过增殖和分化形成成体上皮。在这里,我们回顾了一些证据,表明 T3 诱导的细胞周期程序激活对于 T3 诱导的幼虫上皮细胞死亡和形成成体肠道干细胞很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ebf/10230048/5833d4e1a945/fendo-14-1184013-g001.jpg

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