首页> 外文期刊>Journal of Cell Science >Promotion of lens epithelial-fiber differentiation by the C-terminus of connexin 45.6 a role independent of gap junction communication.
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Promotion of lens epithelial-fiber differentiation by the C-terminus of connexin 45.6 a role independent of gap junction communication.

机译:连接蛋白45.6的C末端促进晶状体上皮纤维分化,其作用独立于间隙连接通讯。

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We previously reported that, among the three connexins expressed in chick lens, overexpression of connexin (Cx) 45.6, not Cx43 or Cx56, stimulates lens cell differentiation; however, the underlying mechanism responsible for this effect is unclear. Here, we took advantage of naturally occurring loss-of-gap-junction function mutations of Cx50 (ortholog of chick Cx45.6) and generated the corresponding site mutants in Cx45.6: Cx45.6(D47A) and Cx45.6(P88S). In contrast to wild-type Cx45.6, the mutants failed to form functional gap junctions, and Cx45.6(P88S) and, to a lesser degree, Cx45.6(D47A) functioned in a dominant-negative manner. Interestingly, overexpression of both mutants incapable of forming gap junctions significantly increased epithelial-fiber differentiation to a level comparable to that of wild-type Cx45.6. To map the functional domain of Cx45.6, we generated a C-terminus chimera as well as deletion mutants. Overexpression of Cx56(*)45.6C, the mutant in which the C-terminus of Cx56 was replaced with that of Cx45.6, had a stimulatory effect on lens cell differentiation similar to that of Cx45.6. However, cells overexpressing Cx45.6(*)56C, the mutant in which C-terminus of Cx45.6 was replaced with that of Cx56, and Cx45.6(-C), in which the C-terminus was deleted, failed to promote differentiation. Taken together, we conclude that the expression of Cx45.6, but not Cx45.6-dependent gap junction channels, is involved in lens epithelial-fiber cell differentiation, and the C-terminal domain of Cx45.6 plays a predominant role in mediating this process.
机译:我们先前曾报道过,在鸡晶状体中表达的三种连接蛋白中,连接蛋白(Cx)45.6而不是Cx43或Cx56的过度表达会刺激晶状体细胞分化。但是,导致这种效果的潜在机制尚不清楚。在这里,我们利用了Cx50(小鸡Cx45.6的直系同源物)的自然发生的空口缺失功能突变,并在Cx45.6中生成了相应的位点突变体:Cx45.6(D47A)和Cx45.6(P88S )。与野生型Cx45.6相反,突变体未能形成功能性缺口连接,Cx45.6(P88S)和Cx45.6(D47A)在较小的程度上以显性负性方式发挥功能。有趣的是,两个不能形成缺口连接的突变体的过表达将上皮纤维分化显着提高到与野生型Cx45.6相当的水平。为了映射Cx45.6的功能域,我们生成了一个C端嵌合体以及缺失突变体。 Cx56(*)45.6C是Cx56的C末端被Cx45.6取代的突变体,其过表达对晶状体细胞的分化具有与Cx45.6相似的刺激作用。但是,过表达Cx45.6(*)56C(其中Cx45.6的C末端被Cx56取代的突变体)和过表达Cx45.6(-C)(其中的C末端被删除)的细胞无法表达促进差异化。两者合计,我们得出结论,Cx45.6的表达,而不是依赖Cx45.6的间隙连接通道,不参与晶状体上皮纤维细胞的分化,并且Cx45.6的C末端结构域在介导中起主要作用这个流程。

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