BRAIN AG, Zwingenberg, Germany.
Department of Dermatology, Venerology and Allergology, Clinic of the Goethe-University, Frankfurt am Main, Germany.
Exp Dermatol. 2018 Dec;27(12):1352-1360. doi: 10.1111/exd.13789.
The barrier function of the human epidermis is constantly challenged by environmental osmotic fluctuations. Hypotonic stress triggers cell swelling, which is counteracted by a compensatory mechanism called regulatory volume decrease (RVD) involving volume-regulated anion channels (VRACs). Recently, it was discovered that VRACs are composed of LRRC8 heteromers and that LRRC8A functions as the essential VRAC subunit in various mammalian cell types; however, the molecular identity of VRACs in the human epidermis remains to be determined. Here, we investigated the expression of LRRC8A and its role in hypotonic stress response of human keratinocytes. Immunohistological staining showed that LRRC8A is preferentially localized in basal and suprabasal epidermal layers. RNA sequencing revealed that LRRC8A is the most abundant subunit within the LRRC8 gene family in HaCaT cells as well as in primary normal human epidermal keratinocytes (NHEKs). To determine the contribution of LRRC8A to hypotonic stress response, we generated HaCaT- and NHEK-LRRC8A knockout cells by using CRISPR-Cas9. I influx assays using halide-sensitive YFP showed that LRRC8A is crucially important for mediating VRAC activity in HaCaTs and NHEKs. Moreover, cell volume measurements using calcein-AM dye further revealed that LRRC8A also substantially contributes to RVD. In summary, our study provides new insights into hypotonic stress response and suggests an important role of LRRC8A as VRAC component in human keratinocytes.
人类表皮的屏障功能不断受到环境渗透压波动的挑战。低渗应激会引发细胞肿胀,这会被一种称为调节性体积减少(RVD)的补偿机制所抵消,该机制涉及体积调节阴离子通道(VRAC)。最近,人们发现 VRAC 由 LRRC8 同型二聚体组成,LRRC8A 是各种哺乳动物细胞类型中 VRAC 的必需亚基;然而,人类表皮中 VRAC 的分子身份仍有待确定。在这里,我们研究了 LRRC8A 的表达及其在人角质形成细胞低渗应激反应中的作用。免疫组织化学染色显示,LRRC8A 主要定位于表皮的基底层和上基底层。RNA 测序显示,LRRC8A 是 HaCaT 细胞以及原代正常人表皮角质形成细胞(NHEKs)中 LRRC8 基因家族中最丰富的亚基。为了确定 LRRC8A 对低渗应激反应的贡献,我们使用 CRISPR-Cas9 技术生成了 HaCaT 和 NHEK-LRRC8A 敲除细胞。使用卤化物敏感的 YFP 的 I 流入测定表明,LRRC8A 对于介导 HaCaT 和 NHEK 中的 VRAC 活性至关重要。此外,使用 calcein-AM 染料进行的细胞体积测量进一步表明,LRRC8A 也大大有助于 RVD。总之,我们的研究为低渗应激反应提供了新的见解,并表明 LRRC8A 作为 VRAC 成分在人角质形成细胞中的重要作用。