Greiser Maura, Halaszovich Christian R, Frechen Dirk, Boknik Peter, Ravens Ursula, Dobrev Dobromir, Lückhoff Andreas, Schotten Ulrich
Institut für Physiologie, Universitätsklinikum Aachen, Aachen, Germany.
Naunyn Schmiedebergs Arch Pharmacol. 2007 Aug;375(6):383-92. doi: 10.1007/s00210-007-0174-6. Epub 2007 Jun 26.
A reduction in L-type Ca(2+) current (I (Ca,L)) contributes to electrical remodeling in chronic atrial fibrillation (AF). Whether the decrease in I (Ca,L) is solely due to a reduction in channel proteins remains controversial. Protein tyrosine kinases (PTK) have been described as potent modulators of I (Ca,L) in cardiomyocytes. We studied alpha(1C) L-type Ca(2+) channel subunit expression and the regulation of I (Ca,L) by PTK in chronic AF using PTK inhibitors: genistein, a nonselective inhibitor of PTK, and 4-amino-5-(4-methylphenyl)-7-(t-butyl)pyrazolo-3,4-d-pyrimidine (PP1), a selective inhibitor of src kinases. Furthermore, type-1 and type-2A protein phosphatase activity was measured with phosphorylase as substrate in whole-cell lysates derived from atrial tissue of AF patients. Right atrial appendages were obtained from patients undergoing open-heart surgery. Protein levels of alpha(1C) L-type Ca(2+) channel subunit were determined using Western blot analysis and normalized to the protein amounts of calsequestrin as internal control. The protein concentrations of alpha(1C) did not differ between AF and sinus rhythm (SR; alpha(1C)/calsequestrin: 1.0 +/- 0.1 and 1.2 +/- 0.2, respectively, n = 8 patients). In cardiomyocytes from patients in SR (n = 20 patients), genistein and PP1 both evoked similar increases in I (Ca,L) from 3.0 +/- 0.3 to 6.1 +/- 0.8 pA/pF and from 2.8 +/- 0.4 to 6.1 +/- 0.6 pA/pF, respectively. In cells from AF patients (n = 10 patients), basal I (Ca,L) was significantly lower. In this case, genistein lead to the same relative increase in I (Ca,L) as in SR cells (from 1.46 +/- 0.30 to 3.2 +/- 1.0 pA/pF), whereas no increase was elicited by PP1 suggesting impaired regulation of I (Ca,L) by src kinases in AF. Total and type 1 and type 2A-related phosphatase activities were higher in tissue from patients with chronic AF compared to SR (4.8 +/- 0.4, 2.1 +/- 0.2, and 2.7 +/- 0.4 nmol/mg/min and 3.6 +/- 0.4, 1.3 +/- 0.2, and 2.4 +/- 0.3 nmol/mg/min, respectively, n = 7 patients per group). Downregulation of I (Ca,L) in AF is not due to a reduction in L-type Ca(2+) channel protein expression. Indirect evidence for an impaired src kinase regulation of I (Ca,L) together with an increased phosphatase activity suggests that a complex alteration in the kinase/phosphatase balance leads to I (Ca,L) dysregulation in chronic AF.
L型钙电流(I(Ca,L))降低参与慢性心房颤动(AF)的电重构。I(Ca,L)降低是否仅由通道蛋白减少所致仍存在争议。蛋白酪氨酸激酶(PTK)已被描述为心肌细胞中I(Ca,L)的有效调节剂。我们使用PTK抑制剂:染料木黄酮(一种非选择性PTK抑制剂)和4-氨基-5-(4-甲基苯基)-7-(叔丁基)吡唑并[3,4-d]嘧啶(PP1,一种src激酶选择性抑制剂),研究了慢性AF中α(1C) L型钙通道亚基表达及PTK对I(Ca,L)的调节。此外,以磷酸化酶为底物,在AF患者心房组织的全细胞裂解物中测量1型和2A型蛋白磷酸酶活性。右心耳取自接受心脏直视手术的患者。使用蛋白质印迹分析测定α(1C) L型钙通道亚基的蛋白水平,并将其标准化为肌集钙蛋白的蛋白量作为内对照。AF和窦性心律(SR)患者之间α(1C)的蛋白浓度无差异(α(1C)/肌集钙蛋白分别为1.0±0.1和1.2±0.2,n = 8例患者)。在SR患者的心肌细胞中(n = 20例患者),染料木黄酮和PP1均使I(Ca,L)分别从3.0±0.3 pA/pF和2.8±0.4 pA/pF类似地增加至6.1±0.8 pA/pF和6.1±0.6 pA/pF。在AF患者的细胞中(n = 10例患者),基础I(Ca,L)显著更低。在这种情况下,染料木黄酮使I(Ca,L)产生与SR细胞中相同的相对增加(从1.46±0.30 pA/pF增加至3.2±1.0 pA/pF),而PP1未引起增加,提示AF中src激酶对I(Ca,L)的调节受损。与SR相比,慢性AF患者组织中的总磷酸酶活性以及1型和2A型相关磷酸酶活性更高(每组n = 7例患者,分别为4.8±0.4、2.1±0.2和2.7±0.4 nmol/mg/min以及3.6±0.4、1.3±0.2和2.4±0.3 nmol/mg/min)。AF中I(Ca,L)下调并非由于L型钙通道蛋白表达减少。src激酶对I(Ca,L)调节受损以及磷酸酶活性增加的间接证据表明,激酶/磷酸酶平衡的复杂改变导致慢性AF中I(Ca,L)失调。