Welsh M J, Li M, McCann J D, Clancy J P, Anderson M P
Howard Hughes Medical Institute, University of Iowa College of Medicine, Iowa City 52242.
Ann N Y Acad Sci. 1989;574:44-51. doi: 10.1111/j.1749-6632.1989.tb25131.x.
The observations described herein allow us to make several inferences about PKC and regulation of normal and CF Cl- channels. FIGURE 5 shows a model that summarizes these observations. In this model, for the sake of clarity, we refer to the channel as a single entity, but note that it may consist of multiple subunits and associated proteins. FIGURE 5A shows the channel in an inactivated state following excision from the cell. The channel can be activated by strong membrane depolarization, via an unknown mechanism, or by phosphorylation with PKA or PKC at a low [Ca2+] We speculate that PKA and PKC may phosphorylate and activate the channel at the same site, or region of the channel, because phosphorylation-dependent activation by both is defective in CF. This result suggests that the CF defect might lie in a defective phosphorylation site on the channel, or associated protein, or in the mechanism that converts phosphorylation into a change in channel conformation, such as activation. Activated channels can be inactivated by PKC at a high [Ca2+]. At high [Ca2+], PKC maintains the channel in an inactivated state and it inactivates channels that have been activated by PKC at low [Ca2+], by depolarization, or by PKA. Both activation and inactivation appear to result from phosphorylation; neither can be explained by down-regulation of the channel. There are several possible ways to explain the two opposite effects of PKC on the Cl- channel: different responses may be due to an effect of Ca2+ on the channel, on PKC, or on the interaction between the two.(ABSTRACT TRUNCATED AT 250 WORDS)
本文所述的观察结果使我们能够对蛋白激酶C(PKC)以及正常和囊性纤维化(CF)氯离子通道的调节做出若干推断。图5展示了一个总结这些观察结果的模型。在此模型中,为清晰起见,我们将通道视为一个单一实体,但需注意它可能由多个亚基和相关蛋白组成。图5A显示从细胞中切除后处于失活状态的通道。该通道可通过未知机制被强膜去极化激活,或在低[Ca2+]浓度下被蛋白激酶A(PKA)或PKC磷酸化激活。我们推测PKA和PKC可能在通道的同一部位或区域进行磷酸化并激活通道,因为在CF中两者依赖磷酸化的激活均存在缺陷。这一结果表明CF缺陷可能在于通道或相关蛋白上的磷酸化位点存在缺陷,或者在于将磷酸化转化为通道构象变化(如激活)的机制存在缺陷。激活的通道可在高[Ca2+]浓度下被PKC失活。在高[Ca2+]浓度下,PKC使通道维持在失活状态,并且它会使已被低[Ca2+]浓度下的PKC、去极化或PKA激活的通道失活。激活和失活似乎均由磷酸化导致;两者都不能用通道的下调来解释。有几种可能的方式来解释PKC对氯离子通道的两种相反作用:不同的反应可能是由于Ca2+对通道、对PKC或对两者之间相互作用的影响。(摘要截选至250字)