MUC19在人眼表和泪腺中的表达及其在干燥综合征患者中的变化。

MUC19 expression in human ocular surface and lacrimal gland and its alteration in Sjögren syndrome patients.

作者信息

Yu D F, Chen Y, Han J M, Zhang H, Chen X P, Zou W J, Liang L Y, Xu C C, Liu Z G

机构信息

State Key Laboratory of Ophthalmology of Sun Yat-Sen University, Zhongshan Ophthalmic Center, Ocular Surface Center of Sun Yat-Sen University, Guangzhou, China.

出版信息

Exp Eye Res. 2008 Feb;86(2):403-11. doi: 10.1016/j.exer.2007.11.013. Epub 2007 Nov 28.

Abstract

This study investigated the expression of MUC19, a newly discovered gel-forming mucin gene, in normal human lacrimal functional unit components and its alteration in Sjögren syndrome patients. Real-time PCR and immunohistochemistry were performed to determine the expression of MUC19 and MUC5AC in human cornea, conjunctiva, and lacrimal gland tissues. Conjunctival impression cytology specimens were collected from normal control subjects and Sjögren syndrome patients for Real-time PCR, PAS staining, and immunohistochemistry assays. In addition, conjunctiva biopsy specimens from both groups were examined for the expression differences of MUC19 and MUC5AC at both mRNA and protein level. The MUC19 mRNA was found to be present in cornea, conjunctiva and lacrimal gland tissues. The immunohistochemical staining of mucins showed that MUC19 was expressed in epithelial cells from corneal, conjunctival, and lacrimal gland tissues. In contrast, MUC5AC mRNA was only present in conjunctiva and lacrimal gland tissues, but not in cornea. Immunostaining demonstrates the co-staining of MUC19 and MUC5AC in conjunctival goblet cells. Consistent with the significant decrease of mucous secretion, both MUC19 and MUC5AC were decreased in conjunctiva of Sjögren syndrome patients compared to normal subjects. Considering the contribution of gel-forming mucins to the homeostasis of the ocular surface, the decreased expression of MUC19 and MUC5AC in Sjögren syndrome patients suggested that these mucins may be involved in the disruption of the ocular surface homeostasis in this disease.

摘要

本研究调查了新发现的凝胶形成粘蛋白基因MUC19在正常人泪液功能单位各组成部分中的表达及其在干燥综合征患者中的变化。采用实时荧光定量PCR和免疫组织化学方法检测人角膜、结膜和泪腺组织中MUC19和MUC5AC的表达。从正常对照者和干燥综合征患者中采集结膜印迹细胞学标本,进行实时荧光定量PCR、PAS染色和免疫组织化学检测。此外,对两组的结膜活检标本进行检测,观察MUC19和MUC5AC在mRNA和蛋白水平的表达差异。发现MUC19 mRNA存在于角膜、结膜和泪腺组织中。粘蛋白的免疫组织化学染色显示,MUC19在角膜、结膜和泪腺组织的上皮细胞中表达。相比之下,MUC5AC mRNA仅存在于结膜和泪腺组织中,而不存在于角膜中。免疫染色显示结膜杯状细胞中MUC19和MUC5AC共染色。与粘液分泌显著减少一致,干燥综合征患者结膜中的MUC19和MUC5AC均低于正常受试者。考虑到凝胶形成粘蛋白对眼表稳态的作用,干燥综合征患者中MUC19和MUC5AC表达降低表明这些粘蛋白可能参与了该疾病眼表稳态的破坏。

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