Augmentation of Cav3.2 T-type calcium channel activity by cAMP-dependent protein kinase A
Augmentation of Cav3.2 T-type calcium channel activity by cAMP-dependent protein kinase A
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DOI：
10.1124/jpet.106.101402
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发表时间：
2006-07-01
影响因子：
3.5
通讯作者：
Lee, Jung-Ha
中科院分区：
文献类型：
--
作者：
Kim, Jin-Ah;Park, Jin-Yong;Lee, Jung-Ha
Ca2+ influx through T-type Ca2+ channels is crucial for important physiological activities such as hormone secretion and neuronal excitability. However, it is not clear whether these channels are regulated by cAMP-dependent protein kinase A (PKA). In the present study, we examined whether PKA modulates Ca(v)3.2T-type channels reconstituted in Xenopus oocytes. Application of 10 mu M forskolin, an adenylyl cyclase stimulant, increased Ca(v)3.2 channel activity by 40 +/- 4% over 30 min and negatively shifted the steady-state inactivation curve (V-50 = -61.4 +/- 0.2 versus -65.5 +/- 0.1 mV). Forskolin did not affect other biophysical properties of Cav3.2 channels, including activation curve, current kinetics, and recovery from inactivation. Similar stimulation was achieved by applying 200 mu M 8-bromo-cAMP, a membrane-permeable cAMP analog. The augmentation of Cav3.2 channel activity by forskolin was strongly inhibited by preincubation with 20 mu M N-[2-(4-bromocinnamylamino) ethyl]-5-isoquinoline (H89), and reversed by subsequent application of 500 nM protein kinase A inhibitor peptide. The stimulation of Ca(v)3.2 channel activity by PKA was mimicked by serotonin when 5HT7 receptor was coexpressed with Ca(v)3.2 in Xenopus oocytes. Finally, using chimeric channels constructed by replacing individual cytoplasmic loops of Cav3.2 with those of the Na(v)1.4 channel, which is insensitive to PKA, we localized a region required for the PKA-mediated augmentation to the II-III loop of the Ca(v)3.2.
