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人眼表上皮和泪液中唾液酸黏蛋白复合物(MUC4)的检测

Detection of sialomucin complex (MUC4) in human ocular surface epithelium and tear fluid.

作者信息

Pflugfelder S C, Liu Z, Monroy D, Li D Q, Carvajal M E, Price-Schiavi S A, Idris N, Solomon A, Perez A, Carraway K L

机构信息

Ocular Surface and Tear Center, Bascom Palmer Eye Institute, University of Miami School of Medicine, Florida 33136, USA.

出版信息

Invest Ophthalmol Vis Sci. 2000 May;41(6):1316-26.

Abstract

PURPOSE

To evaluate human ocular surface epithelium and tear fluid for the presence of sialomucin complex (MUC4), a high-molecular-weight heterodimeric glycoprotein composed of mucin (ASGP-1) and transmembrane (ASGP-2) subunits.

METHODS

Reverse transcription-polymerase chain reaction (RT-PCR) and Northern blot analysis assays were used to identify sialomucin complex RNA in ocular surface epithelia. Immunoprecipitation and immunoblot analysis were used to identify immunoreactive species in human tears and in the corneal and conjunctival epithelia using antibodies specific for carbohydrate and peptide epitopes on the sialomucin complex subunits. Immunofluorescence staining was used to detect sialomucin complex in frozen sections and impression cytology specimens of human cornea and conjunctival epithelia.

RESULTS

ASGP-1- and ASGP-2-specific sequences were amplified from RNA extracted from both conjunctival and corneal epithelial biopsies by RT-PCR. Sialomucin complex transcripts were also detected in these tissues by Northern blot analysis, with a greater level of RNA detected in the peripheral than the central corneal epithelium. Sialomucin complex was immunoprecipitated from tear fluid samples and both corneal and conjunctival epithelia and detected by immunoblot analysis with specific anti-ASGP-1 and anti-ASGP-2 antibodies. The ASGP-1 peptide antibody HA-1 stained the full thickness of the corneal and conjunctival epithelia. In contrast, antibody 15H10, which reacts against a carbohydrate epitope on ASGP-1, stained only the superficial epithelial layers of these tissues. No staining was observed in the conjunctival goblet cells.

CONCLUSIONS

Sialomucin complex was originally identified in rat mammary adenocarcinoma cells and has recently been shown to be produced by the ocular surface epithelia of rats. Furthermore, it has been identified as the rat homologue of human MUC4 mucin. The present studies show that it is expressed in the stratified epithelium covering the surface of the human eye and is present in human tear fluid. Expression of a carbohydrate-dependent epitope on the mucin subunit (ASGP-1) of sialomucin complex occurs in a differentiation-dependent fashion. Sialomucin complex joins MUC1 as another membrane mucin produced by the human ocular surface epithelia but is also found in the tear fluid, presumably in a soluble form, as found on the rat ocular surface.

摘要

目的

评估人眼表上皮和泪液中是否存在涎黏蛋白复合物(MUC4),这是一种由黏蛋白(ASGP - 1)和跨膜蛋白(ASGP - 2)亚基组成的高分子量异二聚体糖蛋白。

方法

采用逆转录 - 聚合酶链反应(RT - PCR)和Northern印迹分析检测眼表上皮中的涎黏蛋白复合物RNA。使用针对涎黏蛋白复合物亚基上碳水化合物和肽表位的特异性抗体,通过免疫沉淀和免疫印迹分析鉴定人泪液、角膜和结膜上皮中的免疫反应性物质。利用免疫荧光染色检测人角膜和结膜上皮冰冻切片及印片细胞学标本中的涎黏蛋白复合物。

结果

通过RT - PCR从结膜和角膜上皮活检组织提取的RNA中扩增出ASGP - 1和ASGP - 2特异性序列。Northern印迹分析也在这些组织中检测到涎黏蛋白复合物转录本,在外周角膜上皮中检测到的RNA水平高于中央角膜上皮。从泪液样本以及角膜和结膜上皮中免疫沉淀出涎黏蛋白复合物,并用特异性抗ASGP - 1和抗ASGP - 2抗体通过免疫印迹分析进行检测。ASGP - 1肽抗体HA - 1对角膜和结膜上皮的全层进行染色。相比之下,与ASGP - 1上碳水化合物表位反应的抗体15H10仅对这些组织的浅表上皮层进行染色。在结膜杯状细胞中未观察到染色。

结论

涎黏蛋白复合物最初在大鼠乳腺腺癌细胞中被鉴定出来,最近已证明它由大鼠眼表上皮产生。此外,它已被鉴定为人MUC4黏蛋白的大鼠同源物。本研究表明,它在覆盖人眼表面的复层上皮中表达,并存在于人泪液中。涎黏蛋白复合物黏蛋白亚基(ASGP - 1)上碳水化合物依赖性表位的表达以分化依赖的方式发生。涎黏蛋白复合物与MUC1一样,是另一种由人眼表上皮产生的膜黏蛋白,但也存在于泪液中,推测是以可溶性形式存在,如同在大鼠眼表面所发现的那样。

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