Coca-Prados M, Fernández-Cabezudo M J, Sánchez-Torres J, Crabb J W, Ghosh S
Department of Ophthalmology and Visual Science, Yale University School of Medicine, New Haven, Connecticut 06510, USA.
Invest Ophthalmol Vis Sci. 1995 Dec;36(13):2717-28.
To evaluate the patterns of expression of beta subunit isoforms of the Na+,K(+)-ATPase and H+,K(+)-ATPase in the human eye and to determine the cell-specific distribution of the beta 2 subunit in the human ciliary epithelium.
Total RNA extracted from human ocular tissues was screened by Northern blot analysis with cDNA probes for the human Na+,K(+)-ATPase subunit isoforms (beta 1 and beta 2) or the H+,K(+)-ATPase (alpha and beta) subunits. Antibodies were raised to the amino and carboxyl terminal regions of the human beta 2 isoform. Polymerase chain reaction was used to verify the expression of beta 2 subunit in nonpigmented ciliary epithelial cells (NPE).
Transcripts for the Na+,K(+)-ATPase beta 1 and beta 2 subunit isoforms were present at different levels in all the ocular tissues except the lens, which expressed only beta 1. No transcripts for the alpha or beta subunits of the H+,K(+)-ATPase were detected in the eye. Isoform beta 2 specific anti-peptide antibodies V15E (N-terminus) and A18R (C-terminus) recognized a 55- to 60-kDa protein in the ciliary epithelium and the core protein of 32 kDa after N-glycanase treatment. Immunocytochemical localization within the ciliary epithelium indicates that the Na+,K(+)-ATPase beta 2 isoform is expressed preferentially in the NPE cells. The expression of Na+,K(+)-ATPase beta 2 isoform in the human NPE cell line, ODM-2, was confirmed by polymerase chain reaction amplification and Southern blot analysis.
The Na+,K(+)-ATPase beta 2 subunit isoform, but not H+,K(+)-ATPase, was expressed widely in ocular tissues of the human eye. The restricted cellular distribution of beta 2 isoform within the NPE cells represents an important differential gene marker associated with the multiple alpha subunit isoforms of Na+,K(+)-ATPase.
评估人眼中Na⁺,K⁺-ATP酶和H⁺,K⁺-ATP酶β亚基同工型的表达模式,并确定β2亚基在人睫状体上皮细胞中的细胞特异性分布。
用人Na⁺,K⁺-ATP酶亚基同工型(β1和β2)或H⁺,K⁺-ATP酶(α和β)亚基的cDNA探针,通过Northern印迹分析筛选从人眼组织中提取的总RNA。制备针对人β2同工型氨基和羧基末端区域的抗体。使用聚合酶链反应验证β2亚基在非色素睫状体上皮细胞(NPE)中的表达。
除晶状体仅表达β1外,Na⁺,K⁺-ATP酶β1和β2亚基同工型的转录本在所有眼组织中均有不同程度的表达。在眼中未检测到H⁺,K⁺-ATP酶α或β亚基的转录本。β2同工型特异性抗肽抗体V15E(N端)和A18R(C端)在睫状体上皮中识别出一种55至60 kDa的蛋白质,N-聚糖酶处理后识别出32 kDa的核心蛋白。睫状体上皮内的免疫细胞化学定位表明,Na⁺,K⁺-ATP酶β2同工型优先在NPE细胞中表达。通过聚合酶链反应扩增和Southern印迹分析证实了Na⁺,K⁺-ATP酶β2同工型在人NPE细胞系ODM-2中的表达。
Na⁺,K⁺-ATP酶β2亚基同工型而非H⁺,K⁺-ATP酶在人眼的眼组织中广泛表达。β2同工型在NPE细胞内的有限细胞分布代表了与Na⁺,K⁺-ATP酶多种α亚基同工型相关的重要差异基因标记。