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国家自然科学基金(30670761)

作品数:3 被引量:4H指数:2
相关作者:刘彦郝丽英赵金生韩冬云封瑞更多>>
相关机构:中国医科大学沈阳药科大学更多>>
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电压门控钙通道钙依赖性易化和失活的分子机制被引量:2
2009年
电压门控钙通道受钙依赖性易化和失活两种相互对立的反馈机制调节。不同浓度的钙离子,通过作为钙感受器的钙调蛋白的介导,主要与钙通道α1亚基羧基端的多个不连续片段发生复杂的相互作用,分别引发钙依赖性易化和失活。钙/钙调蛋白依赖性蛋白激酶Ⅱ及其它钙结合蛋白等也参与此调节过程。新近研究表明,钙通道的钙依赖性调节机制失衡与心律失常等的发病机制密切相关。
刘彦郝丽英
关键词:钙通道钙调蛋白
The roles and relations of calpastatin,calmodulin and an undefined cytoplasmic factor in the regulation of cardiac L-type Ca2+ channels
Objective To explore the mechanism that cytoplasmic factors could recover L-type Ca channel activity after"run...
tsuko MinobeMasaki Kameyama
关键词:CALPASTATINCALMODULINREGULATION
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Calmodulin-and Ca2+-dependent facilitation and inactivation of the CaV1.2 Ca2+ channels in guinea-pig ventricular myocytes
L-type Ca2+channel(Cav1.2)shows clear Ca2+-dependent facilitation(CDF)and inactivation(CDI).Here we have exami...
Masaki Kameyama
关键词:CALMODULIN
豚鼠钙调蛋白1基因的克隆及序列分析被引量:2
2009年
目的克隆豚鼠钙调蛋白1(CaM1)基因,对所克隆基因进行生物信息学分析。方法从豚鼠心室肌组织提取总RNA,应用RT-PCR方法扩增CaM1基因编码区447bp的cDNA片段,插入克隆载体构建重组质粒后基因测序及序列分析。结果克隆出的基因片段编码CaM1全部149个氨基酸,核苷酸序列与多种哺乳动物相应基因的同源性大于90%。获得了该序列的限制性内切酶酶切位点等信息。结论成功获得了豚鼠CaM1基因编码区序列,为进一步重组表达CaM及其功能研究奠定基础。
刘彦封瑞胡慧媛韩冬云赵金生郝丽英
关键词:钙调蛋白RT-PCR基因克隆
Concentration-and calcium-dependent effects of calmodulin and its mutants on L-type Ca2+channel in guinea pig ventricular myocytes
Background:Voltage-gated L-type Ca channel has been suggested to be involved in many essential processes by th...
Kazuto YazawaEtsuko MinobeMasaki Kameyama
关键词:CALMODULIN
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The roles and relations of calpastatin,calmodulin and an undefined cytoplasmic factor in the regulation of cardiac L-type Ca^(2+) channels
2008年
Objective To explore the mechanism that cytoplasmic factors could recover L-type Ca2+ channel activity after "run-down".The factors include ATP,calpastatin and H fraction(a high molecular fraction of bovine cardiac cytoplasm).Methods Single Ca2+ channel activities were recorded with patch clamp technique in guinea-pig cardiac myocytes.Run-down was induced by the inside-out patch formation.Calpastatin(CS),calmodulin(CaM)and three GST-fusion fragment peptides derived from the C-terminal tail of guinea-pig Cav1.2,CT-1(amino acids number 1509-1791),CT-2(1777-2003)and CT-3(1944-2169)were produced as GST fusion proteins.Results(1)CaM + ATP or CS + ATP restored the channels after run-down;however,the CaM or CS's effects became smaller with the longer run-down time.(2)After run down,CaM-dependent protein kinase(CaMKII)produced Ca2+ channel activity to only 2-10% of the basal activity,however,in the presence of CaMKII,the time-dependent nature of the CaM effect was abolished.(3)In pull-down assay,CT-1 treated with CaMKII showed a higher affinity for CaM than that treated with phosphatase.(4)CaMKII was detected in the H fraction of bovine cardiac cytoplasm.Conclusions The results show that CS,CaM and CaMKII are all involved in the maintenance of the basal activity of L-type Ca2+ channels,and that there might be cross talks among the four factors(CS,CaM,CaMKII and the undefined cytoplasmic factor).
tsuko MinobeMasaki Kameyama
关键词:CALPASTATINCALMODULINREGULATION
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