• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

连接蛋白43在发育中的大鼠心脏中的表达。

Expression of connexin43 in the developing rat heart.

作者信息

Fishman G I, Hertzberg E L, Spray D C, Leinwand L A

机构信息

Albert Einstein College of Medicine, Department of Medicine, Bronx, N.Y. 10461.

出版信息

Circ Res. 1991 Mar;68(3):782-7. doi: 10.1161/01.res.68.3.782.

DOI:10.1161/01.res.68.3.782
PMID:1660362
Abstract

Connexin43 is the predominant gap junction protein expressed in the heart. To determine the relation between cardiac maturation and gap junction gene expression, the developmental profiles of connexin43 mRNA and protein were examined in the rat heart. Connexin43 mRNA levels accumulate progressively (eightfold) during embryonic and early neonatal stages, accompanied by a parallel, but temporally delayed, accumulation of connexin43 protein (15-fold). As the heart matures further, both mRNA and protein levels subsequently decline, to about 50% and 30% of their maximum levels, respectively. These observations suggest that increases in intercellular coupling that characterize cardiac development do not depend solely on modulation of connexin43 gene expression, but rather are likely to involve organization of gap junction channels into the intercalated disc.

摘要

连接蛋白43是心脏中表达的主要间隙连接蛋白。为了确定心脏成熟与间隙连接基因表达之间的关系,研究了大鼠心脏中连接蛋白43 mRNA和蛋白质的发育情况。在胚胎期和新生儿早期,连接蛋白43 mRNA水平逐渐积累(增加了八倍),同时连接蛋白43蛋白质也有平行但时间上延迟的积累(增加了15倍)。随着心脏进一步成熟,mRNA和蛋白质水平随后下降,分别降至其最高水平的约50%和30%。这些观察结果表明,心脏发育过程中细胞间偶联增加并非仅取决于连接蛋白43基因表达的调节,而是可能涉及间隙连接通道在闰盘中的组织。

相似文献

1
Expression of connexin43 in the developing rat heart.连接蛋白43在发育中的大鼠心脏中的表达。
Circ Res. 1991 Mar;68(3):782-7. doi: 10.1161/01.res.68.3.782.
2
Spatial distribution of connexin43, the major cardiac gap junction protein, in the developing and adult rat heart.主要心脏间隙连接蛋白连接蛋白43在发育中和成年大鼠心脏中的空间分布。
Circ Res. 1991 Jun;68(6):1638-51. doi: 10.1161/01.res.68.6.1638.
3
Expression of gap junction genes during postnatal neural development.
Dev Genet. 1991;12(4):308-17. doi: 10.1002/dvg.1020120408.
4
Distribution of mRNAs coding for liver and heart gap junction proteins in the rat central nervous system.大鼠中枢神经系统中编码肝脏和心脏间隙连接蛋白的mRNA分布。
J Comp Neurol. 1991 Mar 1;305(1):96-118. doi: 10.1002/cne.903050110.
5
Connexin expression in the developing avian cardiovascular system.
Circ Res. 1993 Jul;73(1):71-8. doi: 10.1161/01.res.73.1.71.
6
Expression of gap junctions in cultured rat L6 cells during myogenesis.大鼠L6细胞在成肌过程中缝隙连接的表达。
Dev Biol. 1993 Feb;155(2):351-60. doi: 10.1006/dbio.1993.1034.
7
Antisera directed against connexin43 peptides react with a 43-kD protein localized to gap junctions in myocardium and other tissues.针对连接蛋白43肽段的抗血清与一种定位于心肌和其他组织缝隙连接的43-kD蛋白发生反应。
J Cell Biol. 1989 Feb;108(2):595-605. doi: 10.1083/jcb.108.2.595.
8
Zygotic expression of the connexin43 gene supplies subunits for gap junction assembly during mouse preimplantation development.连接蛋白43基因的合子表达在小鼠植入前发育过程中为间隙连接组装提供亚基。
Mol Reprod Dev. 1991 Sep;30(1):18-26. doi: 10.1002/mrd.1080300103.
9
Regional differences in connexin32 and connexin43 messenger RNAs in rat brain.大鼠脑中连接蛋白32和连接蛋白43信使核糖核酸的区域差异。
Neurosci Lett. 1990 Apr 6;111(3):297-302. doi: 10.1016/0304-3940(90)90278-h.
10
Immunolabelling patterns of gap junction connexins in the developing and mature rat heart.发育中和成熟大鼠心脏中缝隙连接连接蛋白的免疫标记模式。
Anat Embryol (Berl). 1992;185(4):363-78. doi: 10.1007/BF00188548.

引用本文的文献

1
Recent Advances in Maturation of Pluripotent Stem Cell-Derived Cardiomyocytes Promoted by Mechanical Stretch.机械牵张促进多能干细胞源性心肌细胞成熟的最新进展。
Med Sci Monit. 2021 Aug 12;27:e931063. doi: 10.12659/MSM.931063.
2
Microenvironmental determinants of organized iPSC-cardiomyocyte tissues on synthetic fibrous matrices.在合成纤维基质上,组织化 iPSC 心肌细胞的微环境决定因素。
Biomater Sci. 2021 Jan 5;9(1):93-107. doi: 10.1039/d0bm01247e.
3
Cardiac foetal reprogramming: a tool to exploit novel treatment targets for the failing heart.
心脏胎儿重编程:开发衰竭心脏新型治疗靶点的工具。
J Intern Med. 2020 Nov;288(5):491-506. doi: 10.1111/joim.13094. Epub 2020 Jun 17.
4
Pharmacological and molecular characterization of functional P2 receptors in rat embryonic cardiomyocytes.大鼠胚胎心肌细胞中功能性P2受体的药理学和分子特征
Purinergic Signal. 2015 Mar;11(1):127-38. doi: 10.1007/s11302-014-9441-4. Epub 2014 Dec 16.
5
The Renin-Angiotensin system mediates the effects of stretch on conduction velocity, connexin43 expression, and redistribution in intact ventricle.肾素-血管紧张素系统介导牵张对完整心室传导速度、连接蛋白 43 表达和重分布的影响。
J Cardiovasc Electrophysiol. 2010 Nov;21(11):1276-83. doi: 10.1111/j.1540-8167.2010.01802.x.
6
Connexin40 imparts conduction heterogeneity to atrial tissue.连接蛋白40赋予心房组织传导异质性。
Circ Res. 2008 Oct 24;103(9):1001-8. doi: 10.1161/CIRCRESAHA.107.168997. Epub 2008 Jul 3.
7
Zonula occludens-1 alters connexin43 gap junction size and organization by influencing channel accretion.紧密连接蛋白1通过影响通道积累来改变连接蛋白43间隙连接的大小和组织。
Mol Biol Cell. 2005 Dec;16(12):5686-98. doi: 10.1091/mbc.e05-08-0737. Epub 2005 Sep 29.
8
Redefining the structure of the mouse connexin43 gene: selective promoter usage and alternative splicing mechanisms yield transcripts with different translational efficiencies.重新定义小鼠连接蛋白43基因的结构:选择性启动子使用和可变剪接机制产生具有不同翻译效率的转录本。
Nucleic Acids Res. 2004 Aug 24;32(15):4550-62. doi: 10.1093/nar/gkh792. Print 2004.
9
Evidence for localization of the myotonic dystrophy protein kinase to the terminal cisternae of the sarcoplasmic reticulum.强直性肌营养不良蛋白激酶定位于肌浆网终末池的证据。
J Muscle Res Cell Motil. 1997 Aug;18(4):429-40. doi: 10.1023/a:1018694730773.
10
Characterization and functional studies on rat liver fat-storing cell line and freshly isolated hepatocyte coculture system.大鼠肝贮脂细胞系与新鲜分离肝细胞共培养体系的特性鉴定及功能研究
Am J Pathol. 1995 Jun;146(6):1508-20.