duBell William H, Rogers Terry B
Department of Biochemistry and Molecular Biology, University of Maryland School of Medicine, Baltimore, MD 21201, USA.
J Physiol. 2004 Apr 1;556(Pt 1):79-93. doi: 10.1113/jphysiol.2003.059329. Epub 2004 Jan 23.
Studies have suggested that integration of kinase and phosphatase activities maintains the steady-state L-type Ca(2+) current in ventricular myocytes, a balance disrupted in failing hearts. As we have recently reported that the PP1/PP2A inhibitor calyculin A evokes pronounced increases in L-type I(Ca), the goal of this study was to identify the counteracting kinase and phosphatase that determine 'basal'I(Ca) in isolated mouse ventricular myocytes. Whole-cell voltage-clamp studies, with filling solutions containing 10 mm EGTA, revealed that calyculin A (100 nm) increased I(Ca) at test potentials between -42 and +49 mV (44% at 0 mV) from a holding potential of -80 mV. It also shifted the V(0.5) (membrane potential at half-maximal) of both activation (from -17 to -25 mV) and steady-state inactivation (from -32 to -37 mV) in the hyperpolarizing direction. The broad-spectrum protein kinase inhibitor, staurosporine (300 nm), was without effect on I(Ca) when added after calyculin A. However, by itself, staurosporine decreased I(Ca) throughout the voltage range examined (50% at 0 mV) and blocked the response to calyculin A, indicating that the phosphatase inhibitor's effects depend upon an opposing kinase activity. The PKA inhibitors Rp-cAMPs (100 microm in the pipette) and H89 (1 microm) failed to reduce basal I(Ca) or to block the calyculin A-evoked increase in I(Ca). Likewise, calyculin A was still active with 10 mm intracellular BAPTA or when Ba(2+) was used as the charge carrier. These data eliminate roles for protein kinase A (PKA) and calmodulin-dependent protein kinase II (CaMKII) as counteracting kinases. However, the protein kinase C (PKC) inhibitors Ro 31-8220 (1 microm) and Gö 6976 (200 nm) decreased steady-state I(Ca) and blunted the effect of calyculin A. PP2A is not involved in this regulation as intracellular applications of 10-100 nm okadaic acid or 500 nm fostriecin failed to increase I(Ca). However, PP1 is important, as dialysis with 2 microm okadaic acid or 500 nm inhibitor-2 mimicked the increases in I(Ca) seen with calyculin A. These in situ studies identify constitutive activity of PP1 and the counteracting activity of certain isoforms of PKC, in pathways distinct from receptor-mediated signalling cascades, as regulatory components that determine the steady-state level of cardiac L-type I(Ca).
研究表明,激酶和磷酸酶活性的整合维持了心室肌细胞中L型钙电流的稳态,而这种平衡在衰竭心脏中被打破。正如我们最近报道的,PP1/PP2A抑制剂花萼海绵诱癌素A可引起L型钙电流(I(Ca))显著增加,本研究的目的是确定在分离的小鼠心室肌细胞中决定“基础”I(Ca)的拮抗激酶和磷酸酶。全细胞电压钳研究中,灌流液含有10 mM乙二醇双四乙酸(EGTA),结果显示,从 -80 mV的钳制电位开始,花萼海绵诱癌素A(100 nM)在 -42至 +49 mV的测试电位下增加了I(Ca)(0 mV时增加44%)。它还使激活(从 -17 mV变为 -25 mV)和稳态失活(从 -32 mV变为 -37 mV)的半最大电位(V(0.5))向超极化方向移动。广谱蛋白激酶抑制剂星形孢菌素(300 nM)在花萼海绵诱癌素A之后添加时对I(Ca)没有影响。然而,星形孢菌素本身在整个检测电压范围内降低了I(Ca)(0 mV时降低50%)并阻断了对花萼海绵诱癌素A的反应,表明磷酸酶抑制剂效应取决于一种拮抗激酶活性。蛋白激酶A(PKA)抑制剂Rp-cAMPs(移液管中100 μM)和H89(1 μM)未能降低基础I(Ca)或阻断花萼海绵诱癌素A引起的I(Ca)增加。同样,当细胞内有10 mM 1,2-双(2-氨基苯氧基)乙烷-N,N,N',N'-四乙酸(BAPTA)或使用钡离子(Ba(2+))作为载流子时,花萼海绵诱癌素A仍然有活性。这些数据排除了蛋白激酶A(PKA)和钙调蛋白依赖性蛋白激酶II(CaMKII)作为拮抗激酶的作用。然而,蛋白激酶C(PKC)抑制剂罗-31-8220(1 μM)和戈-6976(200 nM)降低了稳态I(Ca)并减弱了花萼海绵诱癌素A的作用。PP2A不参与此调节,因为细胞内应用10 - 100 nM冈田酸或500 nM福司曲星未能增加I(Ca)。然而,PP1很重要,因为用2 μM冈田酸或500 nM抑制剂-2进行透析可模拟花萼海绵诱癌素A引起的I(Ca)增加。这些原位研究确定了PP1的组成性活性以及PKC某些亚型的拮抗活性,它们在与受体介导的信号级联不同的途径中,作为决定心脏L型I(Ca)稳态水平的调节成分。