Functional analysis of voltage-dependent calcium channel β subunit
Functional analysis of voltage-dependent calcium channel β subunit
批准号:
15590183
负责人:
MURAKAMI Manabu
金额:
$1.98万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2005
中文摘要
1)电压依赖性钙通道的功能作为阳离子通道家族的一员,我们研究了电压依赖性钙通道的功能。分析了电压依赖性钙通道在伤害性神经传递中的作用(Murakami等人,Neuroscience letters,2004,Murakami等人,Brain Res.,2004年)。证明了β3亚基通过增加IP3产生对胰岛素分泌的重要性(Berggren等人,2004年)。评价了全氟辛烷磺酸(PFOS)和全氟辛酸(PFOA)对L型钙通道的抑制作用(Harada等人,2005年)。我们阐明了血栓素A2和前列腺素F2a参与炎性心动过速(Takayama等人,2)鼠PKD2L1(TRPP2L1)的鉴定我们克隆了鼠PKD2L1基因,它是TRP通道家族的成员。PKD2L1通过与PKD1相互作用在质膜上形成功能性阳离子通道(Murakami等人,J. Biol. Chem.,3)TRPC的功能分析使用过表达转基因小鼠,阐明了神经元限制性沉默因子(NRSF)在TRPC 1表达中的调节作用(Ohba等,2005).研究了乌诺前列酮对人主动脉平滑肌细胞中钙池操纵的Ca^2+内流(SOCE)的调节作用(Watanabe等人,2005年)。
英文摘要
1) Functions of voltage-dependent calcium channelsAs a cation channel family member, we investigated functions of voltage-dependent calcium channels. Roles of voltage-dependent calcium channels in nociceptive neurotransmission were analyzed (Murakami et al., Neuroscience letters, 2004, Murakami et al., Brain Res., 2004). Importance of β3 subunit on insulin secretion through increase in IP3 production was proved (Berggren, et al., 2004). Inhibitory effects of perfuorooctane sulfonate (PFOS) and perfuorooctanoate (PFOA) on L-type calcium channels were evaluated (Harada et al., 2005). We clarified involvement of Thromboxane A2 and prostaglandin F2a in inflammatory tachycardia (Takayama et al., 2005).2) Identification of murine PKD2L1 (TRPP2L1)We cloned murine PKD2L1 gene, which is a member of TRP channel family. PKD2L1 forms functional cation channels on the plasma membrane by interacting with PKD1 (Murakami et al., J. Biol. Chem., 2005).3) Functional analysis of TRPCUsing overexpression transgenic mouse, regulatory role of neuron-restrictive silencing factor (NRSF) in expression of TRPC1 was clarified (Ohba et al., 2005).Regulatory effect of unoprostone on store operated Ca^<2+> entry (SOCE) in human aortic smooth muscle cells was investigated (Watanabe et al., 2005).
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Properties and functional roles of T-type Ca^<2+> channels in cardiac pacemaking.
T型Ca^2通道在心脏起搏中的特性和功能作用。
DOI:
--
发表时间:
2005
期刊:
J. Pharmacol. Sci. 99
影响因子:
--
作者:
[Ono, K., Iijima, T.]
通讯作者:
T.
Removal of Ca^<2+> channel β3 subunit enhances Ca^<2+> oscillations frequency and insulin exocytosis.
Ca^2+通道β3亚基的去除增强了Ca^2+振荡频率和胰岛素胞吐作用。
DOI:
--
发表时间:
2004
期刊:
Cell 119
影响因子:
--
作者:
[Berggren, P-O., et al.]
通讯作者:
et al.
Murakami, et al.: "Modified cardiovascular L-type channels in mice lacking the voltage-dependent Ca^<2+> channel β3 subunit"Journal of Biological Chemistry. 278. 43261-43267 (2003)
Murakami等人:“缺乏电压依赖性Ca 2+ 通道β3亚基的小鼠中修饰的心血管L型通道”生物化学杂志278. 43261-43267(2003)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Sevoflurane inhibition of the slowly activating delayed rectifiler K+ current in guineapig ventricular cells
七氟醚抑制豚鼠心室细胞缓慢激活的延迟整流钾电流
DOI:
--
发表时间:
2004
期刊:
J Pharmacol Sci 95
影响因子:
--
作者:
[Shibata, S., Ono, K., Iijima, T.]
通讯作者:
T.
Involvement of voltage-dependent Ca channel β3 subunit in the autonomic control of heart rate variability
电压依赖性 Ca 通道 β3 亚基参与心率变异性自主控制
DOI:
--
发表时间:
2006
期刊:
Pharmacology 76
影响因子:
--
作者:
[Wu, T.W., et. al.]
通讯作者:
et. al.
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