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晶状体纤维细胞分化和细胞器丢失:条条大路通明晰。

Lens fibre cell differentiation and organelle loss: many paths lead to clarity.

机构信息

Ocular Development and Neurobiology Research Group, Zoology Department, School of Natural Sciences, Trinity College Dublin, Dublin 2, Republic of Ireland.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2011 Apr 27;366(1568):1219-33. doi: 10.1098/rstb.2010.0324.

Abstract

The programmed removal of organelles from differentiating lens fibre cells contributes towards lens transparency through formation of an organelle-free zone (OFZ). Disruptions in OFZ formation are accompanied by the persistence of organelles in lens fibre cells and can contribute towards cataract. A great deal of work has gone into elucidating the nature of the mechanisms and signalling pathways involved. It is apparent that multiple, parallel and redundant pathways are involved in this process and that these pathways form interacting networks. Furthermore, it is possible that the pathways can functionally compensate for each other, for example in mouse knockout studies. This makes sense given the importance of lens clarity in an evolutionary context. Apoptosis signalling and proteolytic pathways have been implicated in both lens fibre cell differentiation and organelle loss, including the Bcl-2 and inhibitor of apoptosis families, tumour necrosis factors, p53 and its regulators (such as Mdm2) and proteolytic enzymes, including caspases, cathepsins, calpains and the ubiquitin-proteasome pathway. Ongoing approaches being used to dissect the molecular pathways involved, such as transgenics, lens-specific gene deletion and zebrafish mutants, are discussed here. Finally, some of the remaining unresolved issues and potential areas for future studies are highlighted.

摘要

细胞器从分化的晶状体纤维细胞中被程序性去除,有助于通过形成无细胞器区(OFZ)来保持晶状体透明。OFZ 形成的中断伴随着细胞器在晶状体纤维细胞中的持续存在,并可能导致白内障。人们已经做了大量工作来阐明参与其中的机制和信号通路的性质。显然,这个过程涉及多个平行且冗余的途径,这些途径形成相互作用的网络。此外,这些途径在功能上可能相互补偿,例如在小鼠基因敲除研究中。考虑到晶状体清晰度在进化背景中的重要性,这是有道理的。凋亡信号和蛋白水解途径都与晶状体纤维细胞分化和细胞器丢失有关,包括 Bcl-2 和凋亡抑制因子家族、肿瘤坏死因子、p53 及其调节剂(如 Mdm2)和蛋白水解酶,包括半胱天冬酶、组织蛋白酶、钙蛋白酶和泛素-蛋白酶体途径。这里讨论了正在使用的一些用于剖析相关分子途径的方法,如转基因、晶状体特异性基因缺失和斑马鱼突变体。最后,强调了一些仍然存在的未解决问题和未来研究的潜在领域。

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本文引用的文献

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