Young K C, Peracchia C
Department of Pharmacology and Physiology, School of Medicine and Dentistry, University of Rochester, 575 Elmwood Avenue, Box 711, Rochester, NY 14620, USA.
J Membr Biol. 2004 Dec;202(3):161-70. doi: 10.1007/s00232-004-0727-2.
Previous studies have shown that the V(j)-dependent gating behavior of gap junction channels is altered by CO(2) exposure. V(j)-dependent channel closure is increased by CO(2) in some connexin channels and decreased in others. Since the former type of channels gate on the relatively negative side by V(j) (negative gaters) and the latter at the positive side (positive gaters), it has been hypothesized that gating polarity determines the way CO(2) affects V(j) closure. To test this hypothesis, we have studied the CO(2)-mediated changes in V(j) gating in channels made of Cx32, Cx26, or a Cx32 mutant (Cx32-N2D) in which asparagine (N) at position 2 was replaced with aspartate (D). With exposure to CO(2), Cx32 channels (negative gaters) show increased V(j)-dependent closure, whereas Cx26 channels (positive gaters) respond in the opposite way to V(j). Additionally, Cx32-N2D channels (positive gaters) show decreased V(j) closure with exposure to CO(2). The reciprocal Cx26 mutant, Cx26-D2N (negative gater), could not be tested because it did not express functional homotypic channels. The data support the hypothesis that polarity of fast V(j) gating determines whether CO(2) increases or decreases the V(j) dependent closure of gap junction channels.
先前的研究表明,间隙连接通道的V(j)依赖性门控行为会因二氧化碳暴露而改变。在某些连接蛋白通道中,二氧化碳会增加V(j)依赖性通道关闭,而在其他通道中则会减少。由于前一种类型的通道在相对负侧由V(j)门控(负向门控),后一种在正侧(正向门控),因此有人推测门控极性决定了二氧化碳影响V(j)关闭的方式。为了验证这一假设,我们研究了由Cx32、Cx26或一种Cx32突变体(Cx32-N2D,其中第2位的天冬酰胺(N)被天冬氨酸(D)取代)构成的通道中,二氧化碳介导的V(j)门控变化。暴露于二氧化碳时,Cx32通道(负向门控)显示出V(j)依赖性关闭增加,而Cx26通道(正向门控)对V(j)的反应则相反。此外,Cx32-N2D通道(正向门控)暴露于二氧化碳时显示出V(j)关闭减少。反向的Cx26突变体Cx26-D2N(负向门控)无法进行测试,因为它不表达功能性同型通道。这些数据支持了以下假设:快速V(j)门控的极性决定了二氧化碳是增加还是减少间隙连接通道的V(j)依赖性关闭。