• 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

Rearrangement of intercellular junctions and cytoskeletal proteins during rabbit myocardium development.

作者信息

van der Loop F T, Schaart G, Langmann H, Ramaekers F C, Viebahn C

机构信息

Department of Molecular Cell Biology & Genetics, Cardiovascular Research Institute Maastricht, University of Limburg, The Netherlands.

出版信息

Eur J Cell Biol. 1995 Sep;68(1):62-9.

PMID:8549591
Abstract

A direct and close association between desmosomes and intermediate-sized filaments of the keratin type exists in embryonic and in adult epithelial tissues. Cardiomyocytes are interconnected by spot-desmosomes, which are found in the intercalated disks and can be immunocytochemically detected by antibodies to desmoplakins. In this study, at the light microscopical level, we describe an interaction of keratin filaments with desmoplakins during rabbit myocardiogenesis. In the early stages (0-1 somites), desmoplakins are more abundant in the heart anlagen than in the adjacent intra- and extraembryonic mesoderm. During development of the myocardium, desmoplakin expression gradually rearranges from an apicolateral into an intercalated disk localization in later states. Keratin expression in the developing myocardium of the rabbit heart decreases with the age of the embryo. Keratin filaments are gradually lost via dot-like aggregates which colocalize with desmoplakin-positive clusters. Our results suggest a role for keratins in the developmental rearrangement of desmoplakins into the intercalated disks. A direct relation of desmin and titin reorganization to desmoplakin rearrangement, which was examined because of the dominant role of these proteins in cardiogenesis, was not found.

摘要

相似文献

1
Rearrangement of intercellular junctions and cytoskeletal proteins during rabbit myocardium development.
Eur J Cell Biol. 1995 Sep;68(1):62-9.
2
N-cadherin-catenin interaction: necessary component of cardiac cell compartmentalization during early vertebrate heart development.N-钙黏蛋白-连环蛋白相互作用:脊椎动物早期心脏发育过程中心肌细胞区室化的必要组成部分。
Dev Biol. 1997 May 15;185(2):148-64. doi: 10.1006/dbio.1997.8570.
3
Regulated expression of human filaggrin in keratinocytes results in cytoskeletal disruption, loss of cell-cell adhesion, and cell cycle arrest.人丝聚合蛋白在角质形成细胞中的调控表达导致细胞骨架破坏、细胞间黏附丧失和细胞周期停滞。
Exp Cell Res. 2001 Nov 1;270(2):199-213. doi: 10.1006/excr.2001.5348.
4
Keratin 8 modulation of desmoplakin deposition at desmosomes in hepatocytes.角蛋白8对肝细胞桥粒处桥粒斑蛋白沉积的调节作用。
Exp Cell Res. 2006 Dec 10;312(20):4108-19. doi: 10.1016/j.yexcr.2006.09.031. Epub 2006 Oct 28.
5
Changes in the expression of intermediate filaments and desmoplakins during development of human notochord.
Differentiation. 1995 Jul;59(1):43-9. doi: 10.1046/j.1432-0436.1995.5910043.x.
6
Characterization of cardiotin, a structural component in the myocard.心肌结构成分心肌素的特性研究
Eur J Cell Biol. 1993 Oct;62(1):34-48.
7
Temporal and spatial variations in structural protein expression during the progression from stunned to hibernating myocardium.从顿抑心肌进展为冬眠心肌过程中结构蛋白表达的时空变化。
Circulation. 2004 Nov 23;110(21):3313-21. doi: 10.1161/01.CIR.0000147826.13480.99. Epub 2004 Nov 15.
8
Desmoplakin is required early in development for assembly of desmosomes and cytoskeletal linkage.桥粒斑蛋白在发育早期对于桥粒的组装和细胞骨架连接是必需的。
J Cell Biol. 1998 Dec 28;143(7):2009-22. doi: 10.1083/jcb.143.7.2009.
9
Structural and molecular pathology of the heart in Carvajal syndrome.卡瓦哈尔综合征中心脏的结构与分子病理学
Cardiovasc Pathol. 2004 Jan-Feb;13(1):26-32. doi: 10.1016/S1054-8807(03)00107-8.
10
Transient coexpression of desmin and cytokeratins 8 and 18 in developing myocardial cells of some vertebrate species.
Differentiation. 1988 Sep;38(3):177-93. doi: 10.1111/j.1432-0436.1988.tb00212.x.

引用本文的文献

1
Microtubule-Actin Crosslinking Factor 1 and Plakins as Therapeutic Drug Targets.微管-肌动蛋白交联因子 1 和斑联蛋白作为治疗药物靶点。
Int J Mol Sci. 2018 Jan 26;19(2):368. doi: 10.3390/ijms19020368.
2
Polo-like Kinase 1 Regulates Vimentin Phosphorylation at Ser-56 and Contraction in Smooth Muscle.Polo样激酶1调节波形蛋白Ser-56位点的磷酸化及平滑肌收缩。
J Biol Chem. 2016 Nov 4;291(45):23693-23703. doi: 10.1074/jbc.M116.749341. Epub 2016 Sep 23.
3
Vimentin dephosphorylation at ser-56 is regulated by type 1 protein phosphatase in smooth muscle.
波形蛋白在丝氨酸56处的去磷酸化由平滑肌中的1型蛋白磷酸酶调节。
Respir Res. 2016 Jul 25;17(1):91. doi: 10.1186/s12931-016-0415-7.
4
From stem cells to cardiomyocytes: the role of forces in cardiac maturation, aging, and disease.从干细胞到心肌细胞:力在心脏成熟、衰老和疾病中的作用。
Prog Mol Biol Transl Sci. 2014;126:219-42. doi: 10.1016/B978-0-12-394624-9.00009-9.
5
Requirement of plakophilin 2 for heart morphogenesis and cardiac junction formation.心脏形态发生和心脏连接形成对桥粒芯蛋白2的需求。
J Cell Biol. 2004 Oct 11;167(1):149-60. doi: 10.1083/jcb.200402096.
6
Dedifferentiation of atrial cardiomyocytes as a result of chronic atrial fibrillation.慢性心房颤动导致心房心肌细胞去分化。
Am J Pathol. 1997 Oct;151(4):985-97.