Kindlin1 可调节微管功能,确保有丝分裂正常进行。

Journal De Radiologie Pub Date : 2016-08-01 Epub Date: 2016-03-18 DOI:10.1093/jmcb/mjw009
Hitesh Patel, Ifigeneia Stavrou, Roshan L Shrestha, Viji Draviam, Margaret C Frame, Valerie G Brunton
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引用次数: 0

摘要

Kindlin 1(Kin1)的缺失会导致皮肤大疱性疾病金德勒综合征(KS),其症状还包括皮肤萎缩和角质细胞增殖减少。Kin1 与整合素结合以调节整合素的活化,最近的研究表明,它以一种依赖 Plk1 的方式调节有丝分裂纺锤体和细胞存活。在这里,我们报告了在小鼠皮肤中短期缺失 Kin1 会导致有丝分裂受损,这与乙酰化微管蛋白(ac-tub)水平降低和细胞增殖有关。在细胞中,有丝分裂受阻和乙酰化微管水平降低还伴随着微管稳定性的降低,而所有这些都能通过抑制 HDAC6 得到挽救。Kin1调节依赖于HDAC6的细胞ac-tub水平的能力取决于Plk1对它的磷酸化。综上所述,这些数据确定了 Kin1 在微管乙酰化和稳定性中的新作用,并从机理上揭示了某些 KS 表型(如皮肤萎缩和细胞增殖减少)是如何产生的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Kindlin1 regulates microtubule function to ensure normal mitosis.

Loss of Kindlin 1 (Kin1) results in the skin blistering disorder Kindler Syndrome (KS), whose symptoms also include skin atrophy and reduced keratinocyte proliferation. Kin1 binds to integrins to modulate their activation and more recently it has been shown to regulate mitotic spindles and cell survival in a Plk1-dependent manner. Here we report that short-term Kin1 deletion in mouse skin results in impaired mitosis, which is associated with reduced acetylated tubulin (ac-tub) levels and cell proliferation. In cells, impaired mitosis and reduced ac-tub levels are also accompanied by reduced microtubule stability, all of which are rescued by HDAC6 inhibition. The ability of Kin1 to regulate HDAC6-dependent cellular ac-tub levels is dependent on its phosphorylation by Plk1. Taken together, these data define a novel role for Kin1 in microtubule acetylation and stability and offer a mechanistic insight into how certain KS phenotypes, such as skin atrophy and reduced cell proliferation, arise.

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来源期刊
Journal De Radiologie
Journal De Radiologie 医学-核医学
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