Gründer S, Thiemann A, Pusch M, Jentsch T J
Centre for Molecular Neurobiology (ZMNH), Hamburg University, Germany.
Nature. 1992;360(6406):759-62. doi: 10.1038/360759a0.
Regulation of cell volume is essential for every cell and is accomplished by the regulated loss or gain of intracellular ions or other osmolytes. Regulatory volume decrease often involves the parallel activation of potassium and chloride channels. Overexpression of P-glycoprotein leads to volume-activated Cl- currents but its physiological importance for volume regulation is unclear. CIC-2 is a ubiquitously expressed Cl- channel activatable by non-physiologically strong hyperpolarization. We now show that CIC-2 can be activated by extracellular hypotonicity, which suggests that it has a widespread role in volume regulation. Domains necessary for activation by both voltage and volume are localized to the amino terminus. Mutations in an 'essential' region lead to constitutively open channels unresponsive to medium tonicity, whereas deletions in a 'modulating' region produce partially opened channels responsive to both hypo- and hypertonicity. These domains can be transplanted to different regions of the protein without loss of function.
细胞体积调节对每个细胞都至关重要,它通过细胞内离子或其他渗透溶质的有调控的丢失或增加来实现。调节性体积减小通常涉及钾通道和氯通道的平行激活。P-糖蛋白的过表达会导致体积激活的氯电流,但其对体积调节的生理重要性尚不清楚。CIC-2是一种普遍表达的氯通道,可被非生理性强超极化激活。我们现在表明,CIC-2可被细胞外低渗激活,这表明它在体积调节中具有广泛作用。电压和体积激活所必需的结构域定位于氨基末端。“必需”区域的突变导致组成型开放通道,对培养基张力无反应,而“调节”区域的缺失产生对低渗和高渗均有反应的部分开放通道。这些结构域可以移植到蛋白质的不同区域而不丧失功能。