Himmel H M, Rasmusson R L, Strauss H C
Department of Biomedical Engineering, Duke University Medical Center, Durham, North Carolina 27710.
Am J Physiol. 1994 Nov;267(5 Pt 1):C1338-50. doi: 10.1152/ajpcell.1994.267.5.C1338.
Cultured bovine aortic endothelial cells (BAECs) possess an inward rectifier K+ current (IK1), a Ca(2+)-activated K+ current, a nonselective cation current (INS), and a Ca(2+)-activated Cl- current; however, their relative roles remain to be established. In single BAECs, cytosolic free Ca2+ concentration ([Ca2+]i) [K5-fura 2 (50 microM), ratio 340/380 nm] was measured simultaneously with whole cell currents at 22 degrees C. Bradykinin (BK, 2 microM), ATP (10 microM), ionomycin (100 nM), or 2,5-di-(tert-butyl)-1,4-benzohydroquinone (10 microM) were used as agonists. In physiological salt solution (PSS), agonist exposure caused a rapid [Ca2+]i increase, followed by an increase in outward current (greater than -50 mV) and a smaller increase in inward current (greater than -80 mV). Chelation of [Ca2+]i with 1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid attenuated agonist-induced [Ca2+]i and current responses. Inactivation of the cyclooxygenase pathway by acetylsalicyclic acid and ibuprofen (50 microM each) did not affect the BK-induced [Ca2+]i transient but abolished the current response. In K(+)-free solution, agonist-stimulated outward currents (at +50 mV) were 10 times smaller than in PSS and were consistent with the activation of both INS and a Cl- current. In Cl(-)-free solution, the outward current response following agonist exposure was virtually abolished; at the same time, a linear inward current component with a reversal potential near the equilibrium potential for Na+ was activated. The maximal amplitude of the agonist-induced outward current decreased with decreasing symmetrical Cl- concentrations. Our results suggest that 1) IKI is the dominant current in resting BAECs; 2) K+, Cl-, and nonselective cation conductances contribute to the agonist-induced current response; and 3) most of the agonist-induced activation of currents depends on increased [Ca2+]i and is sensitive to cyclooxygenase inhibitors.
培养的牛主动脉内皮细胞(BAECs)具有内向整流钾电流(IK1)、钙激活钾电流、非选择性阳离子电流(INS)和钙激活氯电流;然而,它们的相对作用仍有待确定。在单个BAECs中,于22℃时使用全细胞膜片钳记录电流的同时,用K5 - 氟罗红2(50微摩尔)测量胞质游离钙浓度([Ca2+]i),测量比率为340/380纳米。使用缓激肽(BK,2微摩尔)、三磷酸腺苷(ATP,10微摩尔)、离子霉素(100纳摩尔)或2,5 - 二 - (叔丁基)-1,4 - 苯二酚(10微摩尔)作为激动剂。在生理盐溶液(PSS)中,激动剂暴露导致[Ca2+]i迅速增加,随后外向电流增加(大于 -50毫伏),内向电流增加较小(大于 -80毫伏)。用1,2 - 双(2 - 氨基苯氧基)乙烷 - N,N,N',N' - 四乙酸螯合[Ca2+]i可减弱激动剂诱导的[Ca2+]i和电流反应。用乙酰水杨酸和布洛芬(各50微摩尔)使环氧合酶途径失活并不影响BK诱导的[Ca2+]i瞬变,但消除了电流反应。在无钾溶液中,激动剂刺激的外向电流(在 +50毫伏时)比在PSS中小10倍,并且与INS和氯电流的激活一致。在无氯溶液中,激动剂暴露后的外向电流反应几乎完全消除;同时,激活了一个反转电位接近钠离子平衡电位的线性内向电流成分。激动剂诱导的外向电流的最大幅度随着对称氯浓度的降低而减小。我们的结果表明:1)IKI是静息BAECs中的主要电流;2)钾离子、氯离子和非选择性阳离子电导对激动剂诱导的电流反应有贡献;3)大部分激动剂诱导的电流激活依赖于[Ca2+]i的增加,并且对环氧合酶抑制剂敏感。