Delalande Jean Marie, Nagy Nandor, McCann Conor J, Natarajan Dipa, Cooper Julie E, Carreno Gabriela, Dora David, Campbell Alison, Laurent Nicole, Kemos Polychronis, Thomas Sophie, Alby Caroline, Attié-Bitach Tania, Lyonnet Stanislas, Logan Malcolm P, Goldstein Allan M, Davey Megan G, Hofstra Robert M W, Thapar Nikhil, Burns Alan J
Centre for Immunobiology, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom.
Stem Cells and Regenerative Medicine, Birth Defects Research Centre, UCL Great Ormond Street Institute of Child Health, London, United Kingdom.
Front Mol Neurosci. 2021 Dec 23;14:757646. doi: 10.3389/fnmol.2021.757646. eCollection 2021.
TALPID3/KIAA0586 is an evolutionary conserved protein, which plays an essential role in protein trafficking. Its role during gastrointestinal (GI) and enteric nervous system (ENS) development has not been studied previously. Here, we analyzed chicken, mouse and human embryonic GI tissues with TALPID3 mutations. The GI tract of TALPID3 chicken embryos was shortened and malformed. Histologically, the gut smooth muscle was mispatterned and enteric neural crest cells were scattered throughout the gut wall. Analysis of the Hedgehog pathway and gut extracellular matrix provided causative reasons for these defects. Interestingly, chicken intra-species grafting experiments and a conditional knockout mouse model showed that ENS formation did not require TALPID3, but was dependent on correct environmental cues. Surprisingly, the lack of TALPID3 in enteric neural crest cells (ENCC) affected smooth muscle and epithelial development in a non-cell-autonomous manner. Analysis of human gut fetal tissues with a mutation showed strikingly similar findings compared to the animal models demonstrating conservation of TALPID3 and its necessary role in human GI tract development and patterning.
TALPID3/KIAA0586是一种进化上保守的蛋白质,在蛋白质运输中起重要作用。此前尚未研究过它在胃肠道(GI)和肠神经系统(ENS)发育过程中的作用。在此,我们分析了具有TALPID3突变的鸡、小鼠和人类胚胎GI组织。TALPID3鸡胚胎的胃肠道缩短且畸形。组织学上,肠道平滑肌的模式异常,肠神经嵴细胞散布于整个肠壁。对刺猬信号通路和肠道细胞外基质的分析为这些缺陷提供了成因。有趣的是,鸡种内移植实验和条件性敲除小鼠模型表明,ENS的形成不需要TALPID3,但依赖于正确的环境信号。令人惊讶的是,肠神经嵴细胞(ENCC)中TALPID3的缺失以非细胞自主的方式影响平滑肌和上皮发育。对具有突变的人类肠道胎儿组织的分析显示,与动物模型相比,结果惊人地相似,表明TALPID3具有保守性及其在人类胃肠道发育和模式形成中的必要作用。