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CDX-1和CDX-2在人结肠黏膜中表达,在先天性巨结肠相关小肠结肠炎患者中表达下调。

CDX-1 and CDX-2 are expressed in human colonic mucosa and are down-regulated in patients with Hirschsprung's disease associated enterocolitis.

作者信息

Lui V C, Li L, Sham M H, Tam P K

机构信息

Department of Surgery, University of Hong Kong Medical Centre, Queen Mary Hospital, Pokfulam, SAR, PR China.

出版信息

Biochim Biophys Acta. 2001 Sep 28;1537(2):89-100. doi: 10.1016/s0925-4439(01)00056-4.

Abstract

Caudal type homeobox gene-1 and -2 (CDX-1 and CDX-2), homologues of the Drosophila homeobox gene caudal, encode transcription factors in endoderm derived tissues of the intestine. CDX genes control proliferation and differentiation of intestinal mucosal cells and colon cancer cells. Hirschsprung's Disease (HD) or congenital intestinal aganglionosis, a major developmental anomaly of intestine, which causes functional intestinal obstruction, is frequently associated with enterocolitis. Aetiology of HD-associated enterocolitis (HDEC) remains obscure. Reduction of gut mucosal enteroendocrine cells, and inefficient transfer of the secretory immunoglobulin A across the gut mucosal cell were shown to be associated with enterocolitis in HD patients suggesting that mucosa may directly involve in the pathophysiology of HDEC. This study aims to ascertain whether the CDX-1 and CDX-2 genes, that control the proliferation and differentiation of mucosal cells, play a role in HDEC. Using semi-quantitative reverse transcription-polymerase chain reaction (RT-PCR) and in situ hybridisation, we analysed the expression of CDX-1 and CDX-2 genes in colon specimens of normal controls, necrotising enterocolitis (NEC) infants, and HD patients with and without enterocolitis. We showed for the first time that CDX-1 and CDX-2 genes were expressed in the colonic mucosal epithelium in normal, NEC and in HD infants. However, the expressions of both genes were reduced in patients with HDEC. Our findings suggest that reduced expression of CDX-1 and CDX-2 genes in mucosa may be associated with the development of HDEC.

摘要

尾型同源框基因-1和-2(CDX-1和CDX-2)是果蝇同源框基因尾的同源物,在肠道内胚层衍生组织中编码转录因子。CDX基因控制肠道黏膜细胞和结肠癌细胞的增殖与分化。先天性巨结肠症(HD)或先天性肠道神经节缺失症是一种主要的肠道发育异常,可导致功能性肠梗阻,常伴有小肠结肠炎。HD相关小肠结肠炎(HDEC)的病因仍不明确。肠道黏膜肠内分泌细胞减少以及分泌型免疫球蛋白A跨肠道黏膜细胞的转运效率低下与HD患者的小肠结肠炎有关,这表明黏膜可能直接参与了HDEC的病理生理过程。本研究旨在确定控制黏膜细胞增殖和分化的CDX-1和CDX-2基因是否在HDEC中起作用。我们使用半定量逆转录-聚合酶链反应(RT-PCR)和原位杂交技术,分析了正常对照组、坏死性小肠结肠炎(NEC)婴儿以及有或无小肠结肠炎的HD患者结肠标本中CDX-1和CDX-2基因的表达情况。我们首次发现CDX-1和CDX-2基因在正常、NEC和HD婴儿的结肠黏膜上皮中均有表达。然而,HDEC患者中这两种基因的表达均降低。我们的研究结果表明,黏膜中CDX-1和CDX-2基因表达降低可能与HDEC的发生有关。

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