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连接蛋白45.6的C末端对晶状体上皮-纤维分化的促进作用:一种独立于缝隙连接通讯的作用

Promotion of lens epithelial-fiber differentiation by the C-terminus of connexin 45.6 a role independent of gap junction communication.

作者信息

Banks Eric A, Yu X Sean, Shi Qian, Jiang Jean X

机构信息

Department of Biochemistry, University of Texas Health Science Center, 7703 Floyd Curl Drive, San Antonio, TX 78229-3900, USA.

出版信息

J Cell Sci. 2007 Oct 15;120(Pt 20):3602-12. doi: 10.1242/jcs.000935. Epub 2007 Sep 25.

DOI:10.1242/jcs.000935
PMID:17895360
Abstract

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.

摘要

我们之前报道过,在鸡晶状体中表达的三种连接蛋白中,连接蛋白(Cx)45.6的过表达而非Cx43或Cx56能刺激晶状体细胞分化;然而,造成这种效应的潜在机制尚不清楚。在此,我们利用了Cx50(鸡Cx45.6的直系同源物)自然发生的间隙连接功能丧失突变,并在Cx45.6中产生了相应的位点突变体:Cx45.6(D47A)和Cx45.6(P88S)。与野生型Cx45.6不同,这些突变体无法形成功能性间隙连接,并且Cx45.6(P88S)以及程度稍轻的Cx45.6(D47A)以显性负性方式发挥作用。有趣的是,两种无法形成间隙连接的突变体的过表达显著增加了上皮 - 纤维细胞分化,达到了与野生型Cx45.6相当的水平。为了绘制Cx45.6的功能域,我们构建了一个C末端嵌合体以及缺失突变体。Cx56()45.6C(其中Cx56的C末端被Cx45.6的C末端取代的突变体)的过表达对晶状体细胞分化具有与Cx45.6相似的刺激作用。然而,过表达Cx45.6()56C(其中Cx45.6的C末端被Cx56的C末端取代的突变体)和Cx45.6(-C)(其中C末端被删除)的细胞未能促进分化。综上所述,我们得出结论,Cx45.6的表达而非依赖Cx45.6的间隙连接通道参与晶状体上皮 - 纤维细胞分化,并且Cx45.6的C末端结构域在介导这一过程中起主要作用。

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