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蛋白激酶C与气道杯状细胞中黏蛋白分泌的Ca2+激活

Protein kinase C and Ca2+ activation of mucin secretion in airway goblet cells.

作者信息

Abdullah L H, Conway J D, Cohn J A, Davis C W

机构信息

Cystic Fibrosis/Pulmonary Research and Treatment Center, University of North Carolina, Chapel Hill 27599-7248, USA.

出版信息

Am J Physiol. 1997 Jul;273(1 Pt 1):L201-10. doi: 10.1152/ajplung.1997.273.1.L201.

Abstract

Airway goblet cells secrete mucin in response to ATP and uridine 5'-triphosphate (UTP), but the underlying signal transduction pathways are poorly understood. Cultures of SPOC1 cells (L. H. Abdullah, S. W. Davis, L. Burch, M. Yamauchi, S. H. Randell, P. Nettesheim, and C. W. Davis. Biochem. J. 316: 943-951, 1996) secreted mucin on exposure to phorbol 12-myristate 13-acetate (PMA) [apparent affinity (K0.5) approximately 100 nM] and ionomycin (K0.5 approximately 5 microM) almost fivefold over baseline. Thapsigargin also elicited secretion (K0.5 approximately 20 nM). Ionomycin and PMA together elicited approximately twice the secretion of either agent alone. Overnight exposure to half-maximal PMA abolished the response to maximal doses of UTP and PMA, whereas ionomycin was fully effective. Protein kinase C (PKC) activity in the membrane fraction was increased by maximal doses of PMA and UTP, whereas ionomycin had no effect. PKC inhibitors were relatively ineffective against PMA- and UTP-induced mucin secretion. Human and canine goblet cells in epithelial explants, by video microscopy, underwent exocytosis with ionomycin (1 microM) and PMA (0.1 or 1 microM). SPOC1 cell mucin secretion was not stimulated by forskolin, 8-(4-chlorophenylthio)-adenosine 3',5'-cyclic monophosphate, or 8-bromoguanosine 3',5'-cyclic monophosphate. Cystic fibrosis transmembrane conductance regulator was not detected in SPOC1 cells by Western blotting, and its mRNA was detected by reverse transcriptase polymerase chain reaction (PCR) only as a very weak band and after 55 PCR cycles. Multidrug resistance (MDR1), however, was readily detected by Western blotting, and its mRNA was detected as a major band after 35 PCR cycles. Thus airway goblet cell mucin secretion, distal to receptor activation, may be regulated independently by Ca(2+)- and PKC-dependent pathways. Cystic fibrosis transmembrane conductance regulator and cyclic nucleotides, however, may not play a major role in this secretion.

摘要

气道杯状细胞会响应三磷酸腺苷(ATP)和尿苷5'-三磷酸(UTP)分泌黏蛋白,但其潜在的信号转导途径却知之甚少。SPOC1细胞培养物(L. H. 阿卜杜拉、S. W. 戴维斯、L. 伯奇、M. 山内、S. H. 兰德尔、P. 内特海姆和C. W. 戴维斯。《生物化学杂志》316: 943 - 951, 1996)在暴露于佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)[表观亲和力(K0.5)约为100 nM]和离子霉素(K0.5约为5 μM)时分泌黏蛋白,分泌量比基线水平高出近五倍。毒胡萝卜素也能引发分泌(K0.5约为20 nM)。离子霉素和PMA共同引发的分泌量约为单独使用任何一种试剂时的两倍。过夜暴露于半最大剂量的PMA会消除对最大剂量UTP和PMA的反应,而离子霉素则完全有效。膜组分中的蛋白激酶C(PKC)活性会因最大剂量的PMA和UTP而增加,而离子霉素则无此作用。PKC抑制剂对PMA和UTP诱导的黏蛋白分泌相对无效。通过视频显微镜观察,上皮外植体中的人和犬杯状细胞在离子霉素(1 μM)和PMA(0.1或1 μM)作用下会发生胞吐作用。SPOC1细胞的黏蛋白分泌不受福斯高林、8 -(4 - 氯苯基硫代)-腺苷3',5'-环磷酸单酯或8 - 溴鸟苷3',5'-环磷酸单酯的刺激。通过蛋白质印迹法在SPOC1细胞中未检测到囊性纤维化跨膜传导调节因子,其mRNA仅在55个逆转录聚合酶链反应(PCR)循环后作为一条非常弱的条带被检测到。然而,多药耐药性(MDR1)通过蛋白质印迹法很容易检测到,其mRNA在35个PCR循环后作为主要条带被检测到。因此,受体激活后远端的气道杯状细胞黏蛋白分泌可能由钙(2+)和PKC依赖的途径独立调节。然而,囊性纤维化跨膜传导调节因子和环核苷酸可能在这种分泌中不发挥主要作用。

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