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细胞粘附分子在患有肠道上皮发育异常(簇状肠病)婴儿中的分布。

Distribution of cell adhesion molecules in infants with intestinal epithelial dysplasia (tufting enteropathy).

作者信息

Patey N, Scoazec J Y, Cuenod-Jabri B, Canioni D, Kedinger M, Goulet O, Brousse N

机构信息

Service d'Anatomie et de Cytologie Pathologiques, Hôpital Necker-Enfants Malades, Université René Descartes, Paris, France.

出版信息

Gastroenterology. 1997 Sep;113(3):833-43. doi: 10.1016/s0016-5085(97)70178-1.

Abstract

BACKGROUND & AIMS: Intestinal epithelial dysplasia, or tufting enteropathy, is a newly described clinicopathologic entity with refractory diarrhea in infants. Histological abnormalities include villous atrophy, disorganization of the surface epithelium, and basement membrane abnormalities. The aim of this study was to examine defects in intestinal epithelial cell adhesion, differentiation, or proliferation in the pathogenesis of epithelial dysplasia.

METHODS

Histological, immunohistochemical, and ultrastructural characteristics of epithelial dysplasia in a group of 6 children were compared with those groups with normal small bowel and other villous atrophy (celiac sprue and microvillous inclusion disease). Distribution of adhesion molecules, markers of cell polarization and proliferation, and the phenotype of intraepithelial lymphocytes were determined.

RESULTS

Alterations suggestive of abnormal cell-cell and cell-matrix interactions were present in patients with epithelial dysplasia. They included abnormal distribution of alpha 2 beta 1 integrin along the crypt-villus axis, increased immunohistochemical expression of desmoglein, and ultrastructural changes of desmosomes increased in length and number. No evidence for abnormalities in epithelial cell polarization, proliferation, or T-cell activation was found.

CONCLUSIONS

This study strongly suggests a role played by alterations of cell-cell and cell-matrix interactions in the pathogenesis of epithelial dysplasia.

摘要

背景与目的

肠道上皮发育异常,即绒毛萎缩性小肠病,是一种新描述的临床病理实体,多见于婴儿难治性腹泻。组织学异常包括绒毛萎缩、表面上皮结构紊乱和基底膜异常。本研究旨在探讨上皮发育异常发病机制中肠道上皮细胞黏附、分化或增殖方面的缺陷。

方法

将6例患儿上皮发育异常的组织学、免疫组化及超微结构特征与正常小肠及其他绒毛萎缩性疾病(乳糜泻和微绒毛包涵体病)患儿进行比较。测定黏附分子的分布、细胞极化和增殖标志物以及上皮内淋巴细胞的表型。

结果

上皮发育异常患者存在提示细胞间及细胞与基质相互作用异常的改变。包括α2β1整合素沿隐窝 - 绒毛轴分布异常、桥粒芯糖蛋白免疫组化表达增加以及桥粒超微结构改变,其长度和数量增加。未发现上皮细胞极化、增殖或T细胞活化异常的证据。

结论

本研究有力地提示细胞间及细胞与基质相互作用改变在上皮发育异常发病机制中起作用。

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