Hwang T C, Lu L, Zeitlin P L, Gruenert D C, Huganir R, Guggino W B
Department of Physiology, Johns Hopkins University, Baltimore, MD 21205.
Science. 1989 Jun 16;244(4910):1351-3. doi: 10.1126/science.2472005.
Secretory chloride channels can be activated by adenosine 3',5'-monophosphate (cAMP)-dependent protein kinase in normal airway epithelial cells but not in cells from individuals with cystic fibrosis (CF). In excised, inside-out patches of apical membrane of normal human airway cells and airway cells from three patients with CF, the chloride channels exhibited a characteristic outwardly rectifying current-voltage relation and depolarization-induced activation. Channels from normal tissues were activated by both cAMP-dependent protein kinase and protein kinase C. However, chloride channels from CF patients could not be activated by either kinase. Thus, gating of normal epithelial chloride channels is regulated by both cAMP-dependent protein kinase and protein kinase C, and regulation by both kinases is defective in CF.
在正常气道上皮细胞中,分泌性氯离子通道可被3',5'-环磷酸腺苷(cAMP)依赖性蛋白激酶激活,但在囊性纤维化(CF)患者的细胞中则不能。在从正常人气道细胞和三名CF患者的气道细胞切下的顶端膜内翻片中,氯离子通道呈现出特征性的外向整流电流-电压关系以及去极化诱导的激活。来自正常组织的通道可被cAMP依赖性蛋白激酶和蛋白激酶C激活。然而,CF患者的氯离子通道不能被任何一种激酶激活。因此,正常上皮氯离子通道的门控受cAMP依赖性蛋白激酶和蛋白激酶C两者调节,且在CF中这两种激酶的调节均存在缺陷。