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药物诱导的先天性巨结肠症鸡模型揭示了糖皮质激素在肠道神经节缺失中的意外作用。

A chicken model of pharmacologically-induced Hirschsprung disease reveals an unexpected role of glucocorticoids in enteric aganglionosis.

作者信息

Gasc Jean-Marie, Clemessy Maud, Corvol Pierre, Kempf Hervé

机构信息

Centre Interdisciplinaire de Recherche Biomédicale (CIRB), Collège de France, 75005 Paris, France Chaire de Médecine Expérimentale, Collège de France, 75005 Paris, France.

Centre Interdisciplinaire de Recherche Biomédicale (CIRB), Collège de France, 75005 Paris, France Chaire de Médecine Expérimentale, Collège de France, 75005 Paris, France Centre de Recherche St-Antoine UMRS-938, INSERM-Université Pierre et Marie Curie, Paris 6, 75012 Paris, France.

出版信息

Biol Open. 2015 Apr 2;4(5):666-71. doi: 10.1242/bio.201410454.

Abstract

The enteric nervous system originates from neural crest cells that migrate in chains as they colonize the embryonic gut, eventually forming the myenteric and submucosal plexus. Failure of the neural crest cells to colonize the gut leads to aganglionosis in the terminal gut, a pathological condition called Hirschsprung disease (HSCR) in humans, also known as congenital megacolon or intestinal aganglionosis. One of the characteristics of the human HSCR is its variable penetrance, which may be attributable to the interaction between genetic factors, such as the endothelin-3/endothelin receptor B pathway, and non-genetic modulators, although the role of the latter has not well been established. We have created a novel HSCR model in the chick embryo allowing to test the ability of non-genetic modifiers to alter the HSCR phenotype. Chick embryos treated by phosphoramidon, which blocks the generation of endothelin-3, failed to develop enteric ganglia in the very distal bowel, characteristic of an HSCR-like phenotype. Administration of dexamethasone influenced the phenotype, suggesting that glucocorticoids may be environmental modulators of the penetrance of the aganglionosis in HSCR disease.

摘要

肠神经系统起源于神经嵴细胞,这些细胞在定殖于胚胎肠道时呈链状迁移,最终形成肌间神经丛和黏膜下神经丛。神经嵴细胞未能定殖于肠道会导致终末肠道神经节缺失,这在人类中是一种被称为先天性巨结肠或肠神经节缺失症的病理状况,在人类中被称为先天性巨结肠或肠神经节缺失症。人类先天性巨结肠的特征之一是其可变的外显率,这可能归因于遗传因素(如内皮素 - 3/内皮素受体B途径)与非遗传调节因子之间的相互作用,尽管后者的作用尚未完全明确。我们在鸡胚中创建了一种新型先天性巨结肠模型,用于测试非遗传修饰因子改变先天性巨结肠表型的能力。用磷酰胺处理的鸡胚,磷酰胺会阻断内皮素 - 3的生成,在最远端肠道未能发育出肠神经节,这是先天性巨结肠样表型的特征。地塞米松的给药影响了表型,表明糖皮质激素可能是先天性巨结肠疾病中神经节缺失外显率的环境调节因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b034/4434818/4b06c53c4e2a/bio-04-05-666-f01.jpg

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