Niisato N, Marunaka Y
Department of Cellular and Molecular Physiology, Kyoto Prefectural University of Medicine, Kyoto, 602-0841, Japan.
Biochem Biophys Res Commun. 2001 Jul 27;285(4):880-4. doi: 10.1006/bbrc.2001.5251.
Forskolin induced the transepithelial Cl- transport (secretion) by activating the apical Cl- channel and basolateral Na+/K+/2Cl- cotransporter in renal epithelial A6 cells via an increase in cytosolic cAMP concentration. The cAMP activation of apical Cl- channel and Na+/K+/2Cl- cotransporter was partially mediated through a protein kinase A (PKA)-dependent pathway, but a PKA-independent pathway was also suggested to be involved in the cAMP activation. Therefore, we assessed a possibility of involvement of protein tyrosine kinase (PTK)-dependent pathway as a PKA-independent pathway in the cAMP activation by applying a PTK inhibitor, tyrphostin A23 (AG18). Tyrphostin A23 abolished the forskolin-induced transepithelial Cl- secretion by partially diminishing the activity of the Cl- channel and completely inhibiting the Na+/K+/2Cl- cotransporter. Further, forskolin increased phosphorylation of protein tyrosine, suggesting that cAMP activates PTK. These observations suggest that cAMP activates the Cl- channel and the Na+/K+/2Cl- cotransporter by activating PTK.
福斯高林通过增加胞质环磷酸腺苷(cAMP)浓度,激活肾上皮A6细胞顶端的氯离子通道和基底外侧的钠/钾/2氯协同转运体,从而诱导跨上皮氯离子转运(分泌)。顶端氯离子通道和钠/钾/2氯协同转运体的cAMP激活部分是通过蛋白激酶A(PKA)依赖性途径介导的,但也提示一条不依赖PKA的途径参与了cAMP激活。因此,我们通过应用蛋白酪氨酸激酶(PTK)抑制剂 tyrphostin A23(AG18),评估了作为不依赖PKA途径的PTK依赖性途径参与cAMP激活的可能性。Tyrphostin A23通过部分降低氯离子通道活性和完全抑制钠/钾/2氯协同转运体,消除了福斯高林诱导的跨上皮氯离子分泌。此外,福斯高林增加了蛋白酪氨酸的磷酸化,提示cAMP激活PTK。这些观察结果表明,cAMP通过激活PTK来激活氯离子通道和钠/钾/2氯协同转运体。