Ebihara L, Xu X, Oberti C, Beyer E C, Berthoud V M
Department of Physiology and Biophysics, Finch University of Health Sciences/The Chicago Medical School, North Chicago, Illinois 60064,
Biophys J. 1999 Jan;76(1 Pt 1):198-206. doi: 10.1016/S0006-3495(99)77189-4.
Lens fiber cells contain two gap junction proteins (Cx56 and Cx45.6 in the chicken). Biochemical studies have suggested that these two proteins can form heteromeric connexons. To investigate the biophysical properties of heteromeric lens connexons, Cx56 was co-expressed with Cx45.6 (or its mouse counterpart, Cx50) in Xenopus oocytes. Whole-cell and single-channel currents were measured in single oocytes by conventional two-microelectrode voltage-clamp and patch clamp techniques, respectively. Injection of Cx56 cRNA induced a slowly activating, nonselective cation current that activated on depolarization to potentials higher than -10 mV. In contrast, little or no hemichannel current was induced by injection of Cx50 or Cx45.6 cRNA. Co-expression of Cx56 with Cx45.6 or Cx50 led to a shift in the threshold for activation to -40 or -70 mV, respectively. It also slowed the rate of deactivation of the hemichannel currents. Moreover, an increase in the unitary conductance, steady state probability of hemichannel opening and mean open times at negative potentials, was observed in (Cx56 + Cx45.6) cRNA-injected oocytes compared with Cx56 cRNA-injected oocytes. These results indicate that co-expression of lens fiber connexins gives rise to novel channels that may be explained by the formation of heteromeric hemichannels that contain both connexins.
晶状体纤维细胞含有两种间隙连接蛋白(鸡体内为Cx56和Cx45.6)。生化研究表明,这两种蛋白可形成异源连接子。为了研究晶状体异源连接子的生物物理特性,将Cx56与Cx45.6(或其小鼠对应物Cx50)在非洲爪蟾卵母细胞中共表达。分别通过传统的双微电极电压钳和膜片钳技术在单个卵母细胞中测量全细胞电流和单通道电流。注射Cx56的cRNA会诱导一种缓慢激活的非选择性阳离子电流,该电流在去极化至高于 -10 mV的电位时激活。相比之下,注射Cx50或Cx45.6的cRNA几乎不诱导或不诱导半通道电流。Cx56与Cx45.6或Cx50共表达分别导致激活阈值向 -40 mV或 -70 mV偏移。这也减缓了半通道电流的失活速率。此外,与注射Cx56的cRNA的卵母细胞相比,在注射(Cx56 + Cx45.6)的cRNA的卵母细胞中观察到单位电导增加、半通道开放的稳态概率增加以及负电位下的平均开放时间增加。这些结果表明,晶状体纤维连接蛋白的共表达产生了新的通道,这可能是由包含两种连接蛋白的异源半通道的形成来解释的。