体积调节阴离子通道LRRC8参与表皮分化的启动,并在银屑病中失调

Magdalena Jahn , Victoria Lang , Oliver Rauh , Torsten Fauth , Claudia Buerger
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引用次数: 0

摘要

最近的研究表明,LRRC8A主要定位于表皮的基底层,是负责调节低渗应激时细胞体积调节的体积调节阴离子通道LRRC8的重要亚基。这促使我们研究LRRC8A是否通过调节该层启动的关键过程(如细胞增殖和/或分化)在维持表皮稳态中发挥作用。LRRC8A在分化开始时的瞬时扩增细胞中被发现强烈上调。当角化细胞进一步成熟时,LRRC8A mRNA仍保持高水平,但LRRC8A蛋白急剧下调。在这一步骤中干扰LRRC8A的表达会抑制角质形成细胞干细胞向瞬时扩增细胞的转变,并损害终末分化。银屑病是一种常见的慢性炎症性皮肤病,以表皮分化紊乱和瞬时扩增细胞功能异常为特征,我们研究了LRRC8A在银屑病中的作用。事实上,LRRC8A在病变性银屑病皮肤中强烈减少,这也可以用Th1/Th17细胞因子混合物在体外模拟。因此,我们的数据表明,LRRC8可以通过恢复角质形成细胞启动分化的能力,作为银屑病病灶局部治疗策略的治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Volume-Regulated Anion Channel LRRC8 is Involved in the Initiation of Epidermal Differentiation and is Deregulated in Psoriasis

The Volume-Regulated Anion Channel LRRC8 is Involved in the Initiation of Epidermal Differentiation and is Deregulated in Psoriasis
Recent studies have shown that LRRC8A, the essential subunit of the volume-regulated anion channel LRRC8, which is responsible for mediating cell volume regulation during hypotonic stress, is predominantly localized in the basal layer of the epidermis. This prompted us to investigate whether LRRC8A plays a role in maintaining epidermal homeostasis by regulating key processes initiated in this layer, such as cell proliferation and/or differentiation.
LRRC8A was found to be strongly upregulated in transiently amplifying cells at the onset of differentiation. While LRRC8A mRNA remains high when keratinocytes mature further, the LRRC8A protein is drastically downregulated. Interference with LRRC8A expression at this step inhibits the transition of keratinocyte stem cells into transiently amplifying cells and impairs terminal differentiation. As psoriasis is a common chronic inflammatory skin disease characterized by disturbed epidermal differentiation and aberrant function of transiently amplifying cells, we investigated the involvement of LRRC8A in this disease. Indeed, LRRC8A was strongly decreased in lesional psoriatic skin, which could also be mimicked in vitro using Th1/Th17 cytokine mixes. Thus, our data suggest that LRRC8 could serve as a therapeutic target for the topical treatment strategies of psoriatic lesions by restoring the capacity of keratinocytes to initiate differentiation.
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