国际麻醉学与复苏杂志
國際痳醉學與複囌雜誌
국제마취학여복소잡지
INTERNATIONAL JOURNAL OF ANESTHESIOLOGY AND RESUSCITATION
2015年
5期
471-474
,共4页
连接蛋白43%缝隙接合部%细胞膜%心律失常,心性
連接蛋白43%縫隙接閤部%細胞膜%心律失常,心性
련접단백43%봉극접합부%세포막%심률실상,심성
Connexin43%Gap junctions%Cell membrane%Arrhythmias,cardiac
背景 缝隙连接蛋白43(connexin43,Cx43)是心肌缝隙连接的主要结构,多种心脏病理过程(如缺血/再灌注等)均可使Cx43重分布至侧膜而发生侧膜化.这种侧膜化使缝隙连接脱耦连,导致折返性心律失常,严重影响心脏的功能.目的 旨在从Cx43转运及定位过程来阐述心肌Cx43侧膜化的分子机制.内容 Cx43侧膜化与闰盘处N钙黏蛋白、桥粒、紧密连接蛋白-1(zonulaoccludens-1,ZO-1)等连接蛋白(connexins,Cxs)的解耦连,以及细胞骨架蛋白介导的Cx43重定向转运密切相关;此外,Cx43的磷酸化、乙酰化也参与了侧膜化的过程.从Cxs、细胞骨架蛋白、磷酸化、乙酰化4个方面就Cx43侧膜化的分子机制展开具体讨论.趋向 为进一步研究Cx43侧膜化机制及临床治疗折返性心律失常提供相关思路及分子基础.
揹景 縫隙連接蛋白43(connexin43,Cx43)是心肌縫隙連接的主要結構,多種心髒病理過程(如缺血/再灌註等)均可使Cx43重分佈至側膜而髮生側膜化.這種側膜化使縫隙連接脫耦連,導緻摺返性心律失常,嚴重影響心髒的功能.目的 旨在從Cx43轉運及定位過程來闡述心肌Cx43側膜化的分子機製.內容 Cx43側膜化與閏盤處N鈣黏蛋白、橋粒、緊密連接蛋白-1(zonulaoccludens-1,ZO-1)等連接蛋白(connexins,Cxs)的解耦連,以及細胞骨架蛋白介導的Cx43重定嚮轉運密切相關;此外,Cx43的燐痠化、乙酰化也參與瞭側膜化的過程.從Cxs、細胞骨架蛋白、燐痠化、乙酰化4箇方麵就Cx43側膜化的分子機製展開具體討論.趨嚮 為進一步研究Cx43側膜化機製及臨床治療摺返性心律失常提供相關思路及分子基礎.
배경 봉극련접단백43(connexin43,Cx43)시심기봉극련접적주요결구,다충심장병리과정(여결혈/재관주등)균가사Cx43중분포지측막이발생측막화.저충측막화사봉극련접탈우련,도치절반성심률실상,엄중영향심장적공능.목적 지재종Cx43전운급정위과정래천술심기Cx43측막화적분자궤제.내용 Cx43측막화여윤반처N개점단백、교립、긴밀련접단백-1(zonulaoccludens-1,ZO-1)등련접단백(connexins,Cxs)적해우련,이급세포골가단백개도적Cx43중정향전운밀절상관;차외,Cx43적린산화、을선화야삼여료측막화적과정.종Cxs、세포골가단백、린산화、을선화4개방면취Cx43측막화적분자궤제전개구체토론.추향 위진일보연구Cx43측막화궤제급림상치료절반성심률실상제공상관사로급분자기출.
Background Connexin43(Cx43) is the major protein of gap junction in the heart.A series of cardiac pathologic processes,such as heart failure and arrhythmias,facilitate Cx43 redistribution to the lateral membrane of the cardiomyocytes from the intercalated disc.The occurrence of gap junctions uncoupling after Cx43 lateralization can lead to reentrant arrhythmias and cardiac dysfunction.Objective To elaborate the molecular mechanisms of myocardial Cx43 lateralization through the process of Cx43 transportation and location.Content The lateralization of Cx43 was proposed to be closely associated with the loss of coupling with connexins (Cxs),i.e.,N-cadherin,desmosomes,Zonula Occludens-1 (ZO-1),and cytoskeletal proteins-mediated forward trafficking of Cx43.Moreover,phosphorylation or acetylation of Cx43 was also involved in its lateralization.This review focusess on the Cxs,cytoskeletal proteins,phosphorylation,and acetylation of Cx43 to show the probable molecular mechanisms of Cx43 lateralization.Trend To provide new ideas and molecular mechanisms for further research into the mechanisms of Cx43 lateralization and the therapy of reentrant arrhythmias.