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钠钾ATP酶α亚基同工型在人睫状体及培养的睫状上皮细胞中的表达

Expression of Na,K-ATPase alpha subunit isoforms in the human ciliary body and cultured ciliary epithelial cells.

作者信息

Martin-Vasallo P, Ghosh S, Coca-Prados M

机构信息

Department of Cell Biology, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

J Cell Physiol. 1989 Nov;141(2):243-52. doi: 10.1002/jcp.1041410203.

Abstract

We have analyzed the expression of Na,K-ATPase alpha subunit isoforms in the transporting ciliary processes of the human eye and in cultured cells derived from non-pigmented (NPE) and pigmented (PE) ciliary epithelium. Northern hybridization analysis shows that the mRNAs encoding all the three distinct forms of Na,K-ATPase alpha subunit [alpha 1, alpha 2, and alpha 3] are expressed in the human ciliary processes in vivo. Immunohistochemical analysis using antibodies specific for each of the three alpha subunit isoforms confirms that these polypeptides are present in the microsomal fraction from the human ciliary processes. The monoclonal antibody McB2, which is specific to the Na,K-ATPase alpha 2 subunit isoform, has been found to decorate specifically the basolateral membrane domains of NPE cells but not of the PE cells, suggesting its expression in vivo only in the ocular NPE ciliary epithelium. However, cultured cells derived from the NPE and PE layers exhibit a different pattern of expression of mRNA and protein for the Na,K-ATPase alpha subunit isoforms when compared to the tissue. Both the NPE and PE cells express alpha 1 and alpha 3 mRNA and polypeptide, whereas alpha 2 mRNA and polypeptide are undetectable in these cells. The established cell lines derived from the NPE layer express comparable levels of the alpha 1 and alpha 3 isoforms of Na,K-ATPase as detected in the primary culture. However, the established NPE cell lines are also distinguishable from the normal PE cells when analyzed by Western blot analysis with A x 2 antibodies. The results presented here clearly show that the NPE and PE cells in the ciliary body have a distinct expression of Na,K-ATPase alpha subunit isoforms as compared to cultured cells.

摘要

我们分析了钠钾ATP酶α亚基同工型在人眼运输性睫状体以及源自非色素(NPE)和色素(PE)睫状体上皮的培养细胞中的表达。Northern杂交分析表明,编码钠钾ATP酶α亚基三种不同形式[α1、α2和α3]的mRNA在人睫状体的体内表达。使用针对三种α亚基同工型各自的特异性抗体进行免疫组织化学分析证实,这些多肽存在于人睫状体的微粒体部分。已发现对钠钾ATP酶α2亚基同工型具有特异性的单克隆抗体McB2特异性地标记NPE细胞的基底外侧膜结构域,而不标记PE细胞的,这表明其仅在眼NPE睫状体上皮中体内表达。然而,与组织相比,源自NPE和PE层的培养细胞显示出钠钾ATP酶α亚基同工型的mRNA和蛋白质表达模式不同。NPE和PE细胞均表达α1和α3 mRNA及多肽,而在这些细胞中检测不到α2 mRNA和多肽。源自NPE层的已建立细胞系表达的钠钾ATP酶α1和α3同工型水平与原代培养中检测到的相当。然而,当用Ax 2抗体进行蛋白质印迹分析时,已建立的NPE细胞系也与正常PE细胞不同。此处呈现的结果清楚地表明,与培养细胞相比,睫状体中的NPE和PE细胞具有钠钾ATP酶α亚基同工型的独特表达。

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