Laboratory of Human and General Physiology, Department of Pharmacy and Biotechnology, University of Bologna, Bologna, Italy.
Institute for the Study of Nanostructured Materials, National Research Council of Italy, Bologna, Italy.
FASEB J. 2019 Jan;33(1):101-113. doi: 10.1096/fj.201701397RR. Epub 2018 Jun 29.
Consolidated evidence indicates that astroglial cells are critical in the homeostatic regulation of cellular volume by means of ion channels and aquaporin-4. Volume-regulated anion channel (VRAC) is the chloride channel that is activated upon cell swelling and critically contributes to cell volume regulation in astrocytes. The molecular identity of VRAC has been recently defined, revealing that it belongs to the leucine-rich repeat-containing 8 (LRRC8) protein family. However, there is a lack of evidence demonstrating that LRRC8A underpins VRAC currents in astrocyte. Nonetheless, direct evidence of the role of LRRC8A in astrocytic regulatory volume decrease remains to be proved. Here, we aim to bridge this gap in knowledge by combining RNA interference specific for LRRC8A with patch-clamp analyses and a water-permeability assay. We demonstrated that LRRC8A molecular expression is essential for swelling-activated chloride current via VRAC in primary-cultured cortical astrocytes. The knockdown of LRRC8A with a specific short interference RNA abolished the recovery of the cell volume after swelling induced by hypotonic challenge. In addition, immunoblotting, immunofluorescence, confocal imaging, and immunogold electron microscopy demonstrated that LRRC8A is expressed in the plasma membrane of primary cortical astrocytes and in situ in astrocytes at the perivascular interface with endothelial cells. Collectively, our results suggest that LRRC8A is an essential subunit of VRAC and a key factor for astroglial volume homeostasis.-Formaggio, F., Saracino, E., Mola, M. G., Rao, S. B., Amiry-Moghaddam, M., Muccini, M., Zamboni, R., Nicchia, G. P., Caprini, M., Benfenati, V. LRRC8A is essential for swelling-activated chloride current and for regulatory volume decrease in astrocytes.
综合证据表明,星形胶质细胞通过离子通道和水通道蛋白-4 对细胞体积的稳态调节起着关键作用。体积调节阴离子通道 (VRAC) 是一种在细胞肿胀时被激活的氯离子通道,对星形胶质细胞的体积调节起着至关重要的作用。VRAC 的分子特征最近已被确定,表明它属于富含亮氨酸重复序列 8 (LRRC8) 蛋白家族。然而,目前缺乏证据表明 LRRC8A 是星形胶质细胞 VRAC 电流的基础。尽管如此,LRRC8A 在星形胶质细胞调节性体积减少中的作用的直接证据仍有待证明。在这里,我们旨在通过结合针对 LRRC8A 的 RNA 干扰与膜片钳分析和水通透性测定来填补这一知识空白。我们证明了 LRRC8A 的分子表达对于原代皮质星形胶质细胞中肿胀激活的氯离子电流通过 VRAC 是必不可少的。用特异性短发夹 RNA 敲低 LRRC8A 会消除由低渗挑战诱导的肿胀后细胞体积的恢复。此外,免疫印迹、免疫荧光、共聚焦成像和免疫金电子显微镜显示,LRRC8A 在原代皮质星形胶质细胞的质膜中以及在与内皮细胞的血管周围界面处的星形胶质细胞中表达。总之,我们的结果表明,LRRC8A 是 VRAC 的必需亚基,也是星形胶质细胞体积稳态的关键因素。