Maehara Hirofumi, Okamura Hiro-oki, Kobayashi Katsuki, Uchida Shinichi, Sasaki Sei, Kitamura Ken
Department of Otorhinolaryngology, Tokyo Medical and Dental University, Japan.
Neuroreport. 2003 Aug 26;14(12):1571-3. doi: 10.1097/00001756-200308260-00006.
We have investigated the expression of chloride channels by examining the cochlea of mice harboring the enhanced green fluorescence protein (EGFP) gene driven by an 11 kbp human CLC-KB gene promoter. CLC-KB was seen not only on the stria vascularis but on spiral ligament and limbal fibrocytes, interdental cells and satellite cells of spiral ganglion neurons that are known to possess both Na,K-ATPase and the Na-K-Cl co-transporter (NKCC). These results suggest that some fibrocytes possessing both the CLC-KB and the NKCC may be involved in the regulation of cell volume, transport and recycling of Cl- such as is seen in the stria vascularis. Moreover, these fibrocytes may recycle Cl- through CLC that accompany Na+ and K+ into the cell via NKCC.
我们通过检查携带由11kbp人CLC-KB基因启动子驱动的增强型绿色荧光蛋白(EGFP)基因的小鼠耳蜗,研究了氯离子通道的表达。不仅在血管纹上,而且在螺旋韧带、边缘纤维细胞、螺旋神经节神经元的齿间细胞和卫星细胞上都观察到了CLC-KB,已知这些细胞同时拥有钠钾ATP酶和钠钾氯共转运体(NKCC)。这些结果表明,一些同时拥有CLC-KB和NKCC的纤维细胞可能参与细胞体积的调节、氯离子的转运和再循环,就像在血管纹中看到的那样。此外,这些纤维细胞可能通过CLC再循环氯离子,CLC伴随钠离子和钾离子通过NKCC进入细胞。