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mCLCA1/2 在鼠胃肠道上皮细胞中的细胞分布和亚细胞定位。

Cellular distribution and subcellular localization of mCLCA1/2 in murine gastrointestinal epithelia.

机构信息

Department of Molecular Embryology, Institute for Anatomy and Cell Biology II, University of Freiburg, Germany.

出版信息

J Histochem Cytochem. 2010 Jul;58(7):653-68. doi: 10.1369/jhc.2010.955211. Epub 2010 Apr 12.

Abstract

mCLCA1/2 are members of the CLCA protein family that are widely expressed in secretory epithelia, but their putative physiological role still awaits elucidation. mCLCA1/2 have 95% amino acid identity, but currently no specific antibody is available. We have generated a rabbit polyclonal antibody (pAb849) against aa 424-443 of mCLCA1/2. In HEK293 cells transfected with mCLCA1; pAb849 detected two specific protein bands at approximately 125 kDa and 90 kDa, representing full-length precursor and N-terminal cleavage product, respectively. pAb849 also immunoprecipitated mCLCA1 and labeled the protein by immunostaining. But pAb849 crossreacted with mCLCA3/4/6 despite < or =80% amino acid identity of the antigenic epitope. We therefore investigated the cellular localization of mCLCA1/2 in epithelial tissues, which do not express mCLCA3/4/6 (salivary glands, pancreas, kidney) or express mCLCA3/6 with known localization (mucus cells of stomach and small intestine; villi of small intestine). mCLCA1/2 mRNA and protein expression were found in both parotid and submandibular gland, and immunohistochemistry revealed labeling in parotid acinar cells, in the luminal membrane of parotid duct cells, and in the duct cells of submandibular gland. In exocrine pancreas, mCLCA1/2 expression was restricted to acinar zymogen granule membranes, as assessed by immunoblotting, immunohistochemistry, and preembedding immunoperoxidase and immunogold electron microscopy. Moreover, mCLCA1/2 immunolabeling was present in luminal membranes of gastric parietal cells and small intestinal crypt enterocytes, whereas in the kidney, mCLCA1/2 protein was localized to proximal and distal tubules. The apical membrane localization and overall distribution pattern of mCLCA1/2 favor a transmembrane protein implicated in transepithelial ion transport and protein secretion.

摘要

mCLCA1/2 是 CLCA 蛋白家族的成员,广泛表达于分泌上皮细胞,但它们的潜在生理作用仍有待阐明。mCLCA1/2 具有 95%的氨基酸同一性,但目前尚无特异性抗体可用。我们针对 mCLCA1/2 的 aa424-443 生成了兔多克隆抗体(pAb849)。在转染 mCLCA1 的 HEK293 细胞中,pAb849 检测到两个约 125 kDa 和 90 kDa 的特异性蛋白条带,分别代表全长前体和 N 端切割产物。pAb849 还可免疫沉淀 mCLCA1,并通过免疫染色标记该蛋白。但是,尽管抗原表位的氨基酸同一性<或=80%,pAb849 仍与 mCLCA3/4/6 发生交叉反应。因此,我们研究了 mCLCA1/2 在不表达 mCLCA3/4/6(唾液腺、胰腺、肾脏)或表达具有已知定位的 mCLCA3/6(胃和小肠的粘液细胞;小肠的绒毛)的上皮组织中的细胞定位。在腮腺和颌下腺中均发现 mCLCA1/2 mRNA 和蛋白表达,免疫组织化学显示标记位于腮腺腺泡细胞、腮腺导管细胞的腔膜和颌下腺导管细胞中。在外分泌胰腺中,mCLCA1/2 的表达仅限于腺泡酶原颗粒膜,这通过免疫印迹、免疫组织化学和包埋前免疫过氧化物酶和免疫金电子显微镜评估。此外,mCLCA1/2 免疫标记存在于胃壁细胞的腔膜和小肠隐窝肠上皮细胞中,而在肾脏中,mCLCA1/2 蛋白定位于近端和远端小管。mCLCA1/2 的顶膜定位和整体分布模式表明其是一种跨膜蛋白,参与跨上皮离子转运和蛋白分泌。

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