Cell Communication and Adhesion最新文献

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Desmosomal cadherins and signaling: lessons from autoimmune disease. 桥粒体钙粘蛋白和信号:来自自身免疫性疾病的教训。
Cell Communication and Adhesion Pub Date : 2014-02-01 DOI: 10.3109/15419061.2013.877000
Volker Spindler, Jens Waschke
{"title":"Desmosomal cadherins and signaling: lessons from autoimmune disease.","authors":"Volker Spindler,&nbsp;Jens Waschke","doi":"10.3109/15419061.2013.877000","DOIUrl":"https://doi.org/10.3109/15419061.2013.877000","url":null,"abstract":"<p><p>Autoantibodies from patients suffering from the autoimmune blistering skin disease pemphigus can be applied as tools to study desmosomal adhesion. These autoantibodies targeting the desmosomal cadherins desmoglein (Dsg) 1 and Dsg3 cause disruption of desmosomes and loss of intercellular cohesion. Although pemphigus autoantibodies were initially proposed to sterically hinder desmosomes, many groups have shown that they activate signaling pathways which cause disruption of desmosomes and loss of intercellular cohesion by uncoupling the desmosomal plaque from the intermediate filament cytoskeleton and/or by interfering with desmosome turnover. These studies demonstrate that desmogleins serve as receptor molecules to transmit outside-in signaling and demonstrate that desmosomal cadherins have functions in addition to their adhesive properties. Two central molecules regulating cytoskeletal anchorage and desmosome turnover are p38MAPK and PKC. As cytoskeletal uncoupling in turn enhances Dsg3 depletion from desmosomes, both mechanisms reinforce one another in a vicious cycle that compromise the integrity and number of desmosomes.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"21 1","pages":"77-84"},"PeriodicalIF":0.0,"publicationDate":"2014-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.877000","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32058280","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 41
Plakophilins in desmosomal adhesion and signaling. 亲血小板蛋白在桥粒黏附和信号传导中的作用。
Cell Communication and Adhesion Pub Date : 2014-02-01 DOI: 10.3109/15419061.2013.876017
Mechthild Hatzfeld, Annika Wolf, René Keil
{"title":"Plakophilins in desmosomal adhesion and signaling.","authors":"Mechthild Hatzfeld,&nbsp;Annika Wolf,&nbsp;René Keil","doi":"10.3109/15419061.2013.876017","DOIUrl":"https://doi.org/10.3109/15419061.2013.876017","url":null,"abstract":"<p><p>The regulation of adhesion and growth is important for epithelial function and dysfunction. β-catenin (armadillo in Drosophila) is the prototype of a multifunctional molecule that regulates cell adhesion via adherens junctions and cell signaling via LEF/TCF transcription factors. Desmosomal armadillo proteins comprise plakoglobin and the plakophilins 1, 2, and 3. These proteins are essential for building up the desmosome and linking the desmosomal cadherins to keratin filaments. High expression of plakophilins in desmosomes correlates with strong intercellular cohesion and is essential for tissue integrity under mechanical stress. However, like β-catenin, these proteins have diverse non-desmosomal functions, for example, in regulating actin organization, protein synthesis, and growth control. In line with these functions, their de-regulated expression with up- as well as down-regulation has been connected to cancer and metastasis. Now, recent evidence sheds light on the post-translational regulation and provides an explanation for how de-regulation of plakophilins can contribute to cancer.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"21 1","pages":"25-42"},"PeriodicalIF":0.0,"publicationDate":"2014-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.876017","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32060467","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 47
Desmosomal adhesion in vivo. 体内桥粒黏附。
Cell Communication and Adhesion Pub Date : 2014-02-01 DOI: 10.3109/15419061.2013.876018
Mohamed Berika, David Garrod
{"title":"Desmosomal adhesion in vivo.","authors":"Mohamed Berika,&nbsp;David Garrod","doi":"10.3109/15419061.2013.876018","DOIUrl":"https://doi.org/10.3109/15419061.2013.876018","url":null,"abstract":"<p><p>Desmosomes are intercellular junctions that provide strong adhesion or hyper-adhesion in tissues. Here, we discuss the molecular and structural basis of this with particular reference to the desmosomal cadherins (DCs), their isoforms and evolution. We also assess the role of DCs as regulators of epithelial differentiation. New data on the role of desmosomes in development and human disease, especially wound healing and pemphigus, are briefly discussed, and the importance of regulation of the adhesiveness of desmosomes in tissue dynamics is considered.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"21 1","pages":"65-75"},"PeriodicalIF":0.0,"publicationDate":"2014-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.876018","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32058277","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 28
Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin 43 localization. 到插入椎间盘的贩运高速公路:解锁连接蛋白43定位特异性的新见解。
Cell Communication and Adhesion Pub Date : 2014-02-01 DOI: 10.3109/15419061.2013.876014
Shan-Shan Zhang, Robin M Shaw
{"title":"Trafficking highways to the intercalated disc: new insights unlocking the specificity of connexin 43 localization.","authors":"Shan-Shan Zhang,&nbsp;Robin M Shaw","doi":"10.3109/15419061.2013.876014","DOIUrl":"https://doi.org/10.3109/15419061.2013.876014","url":null,"abstract":"<p><p>With each heartbeat, billions of cardiomyocytes work in concert to propagate the electrical excitation needed to effectively circulate blood. Regulated expression and timely delivery of connexin proteins to form gap junctions at the specialized cell-cell contact region, known as the intercalated disc, is essential to ventricular cardiomyocyte coupling. We focus this review on several regulatory mechanisms that have been recently found to govern the lifecycle of connexin 43 (Cx43), the short-lived and most abundantly expressed connexin in cardiac ventricular muscle. The Cx43 lifecycle begins with gene expression, followed by oligomerization into hexameric channels, and then cytoskeletal-based transport toward the disc region. Once delivered, hemichannels interact with resident disc proteins and are organized to effect intercellular coupling. We highlight recent studies exploring regulation of Cx43 localization to the intercalated disc, with emphasis on alternatively translated Cx43 isoforms and cytoskeletal transport machinery that together regulate Cx43 gap junction coupling between cardiomyocytes.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"21 1","pages":"43-54"},"PeriodicalIF":0.0,"publicationDate":"2014-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.876014","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"32058279","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 20
Patterns in space: coordinating adhesion and actomyosin contractility at E-cadherin junctions. 空间模式:在e -钙粘蛋白连接处协调粘附和肌动球蛋白收缩。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-08 DOI: 10.3109/15419061.2013.856889
Selwin Kaixiang Wu, Alpha S Yap
{"title":"Patterns in space: coordinating adhesion and actomyosin contractility at E-cadherin junctions.","authors":"Selwin Kaixiang Wu,&nbsp;Alpha S Yap","doi":"10.3109/15419061.2013.856889","DOIUrl":"https://doi.org/10.3109/15419061.2013.856889","url":null,"abstract":"<p><p>Cadherin adhesion receptors are fundamental determinants of tissue organization in health and disease. Increasingly, we have come to appreciate that classical cadherins exert their biological actions through active cooperation with the contractile actin cytoskeleton. Rather than being passive resistors of detachment forces, cadherins can regulate the assembly and mechanics of the contractile apparatus itself. Moreover, coordinate spatial patterning of adhesion and contractility is emerging as a determinant of morphogenesis. Here we review recent developments in cadherins and actin cytoskeleton cooperativity, by focusing on E-cadherin adhesive patterning in the epithelia. Next, we discuss the underlying principles of cellular rearrangement during Drosophila germband extension and epithelial cell extrusion, as models of how planar and apical-lateral patterns of contractility organize tissue architecture.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"201-12"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.856889","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31846225","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 34
A century of cell adhesion: from the blastomere to the clinic part 1: conceptual and experimental foundations and the pre-molecular era. 一个世纪的细胞粘附:从卵裂球到临床第一部分:概念和实验基础和前分子时代。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-19 DOI: 10.3109/15419061.2013.858713
Gerald B Grunwald
{"title":"A century of cell adhesion: from the blastomere to the clinic part 1: conceptual and experimental foundations and the pre-molecular era.","authors":"Gerald B Grunwald","doi":"10.3109/15419061.2013.858713","DOIUrl":"https://doi.org/10.3109/15419061.2013.858713","url":null,"abstract":"<p><p>The historical roots of cell adhesion research stretch back over a hundred years, commencing with fundamental questions from the advent of experimental embryology in the late nineteenth century. The transition of embryology from a descriptive to an experimentally driven and mechanistic branch of the biological sciences included investigations focused on the interactions of the first cells of the newly developing embryo, the blastomeres, and followed the movement, interactions and fate of these cells as the tissues and organs of the growing embryo took form. Of special interest to early investigators were cell-cell contacts, which were obviously dynamic but of an obscure nature. This historical review, the first of a series, explores the early years of the cell adhesion field, including the work of Roux, Wilson, Galtsoff, Just and Holtfreter, and discusses the classical experiments, observations and conceptual developments that formed the cornerstone of cell adhesion research during its premolecular era.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"127-38"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.858713","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31876059","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Structural and functional diversity of desmosomes. 桥粒的结构和功能多样性。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-08 DOI: 10.3109/15419061.2013.855204
Robert M Harmon, Kathleen J Green
{"title":"Structural and functional diversity of desmosomes.","authors":"Robert M Harmon,&nbsp;Kathleen J Green","doi":"10.3109/15419061.2013.855204","DOIUrl":"https://doi.org/10.3109/15419061.2013.855204","url":null,"abstract":"<p><p>Desmosomes anchor intermediate filaments at sites of cell contact established by the interaction of cadherins extending from opposing cells. The incorporation of cadherins, catenin adaptors, and cytoskeletal elements resembles the closely related adherens junction. However, the recruitment of intermediate filaments distinguishes desmosomes and imparts a unique function. By linking the load-bearing intermediate filaments of neighboring cells, desmosomes create mechanically contiguous cell sheets and, in so doing, confer structural integrity to the tissues they populate. This trait and a well-established role in human disease have long captured the attention of cell biologists, as evidenced by a publication record dating back to the mid-1860s. Likewise, emerging data implicating the desmosome in signaling events pertinent to organismal development, carcinogenesis, and genetic disorders will secure a prominent role for desmosomes in future biological and biomedical investigations.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"171-87"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.855204","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31846224","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 42
Signaling and mechanical roles of E-cadherin. e -钙粘蛋白的信号传导和机械作用。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-08 DOI: 10.3109/15419061.2013.854778
Tanay Bhatt, Abrar Rizvi, Surya Prakash Rao Batta, Sunny Kataria, Colin Jamora
{"title":"Signaling and mechanical roles of E-cadherin.","authors":"Tanay Bhatt,&nbsp;Abrar Rizvi,&nbsp;Surya Prakash Rao Batta,&nbsp;Sunny Kataria,&nbsp;Colin Jamora","doi":"10.3109/15419061.2013.854778","DOIUrl":"https://doi.org/10.3109/15419061.2013.854778","url":null,"abstract":"<p><p>The epithelium comprises an important tissue that lines the internal and external surfaces of metazoan organs. In order to organize sheets of epithelial cells into three-dimensional tissues, it requires the coordination of basic cellular processes such as polarity, adhesion, growth, and differentiation. Moreover, as a primary barrier to the external environment, epithelial tissues are often subjected to physical forces and damage. This critical barrier function dictates that these fundamental cellular processes are continually operational in order to maintain tissue homeostasis in the face of almost constant trauma and stress. A protein that is largely responsible for the organization and maintenance of epithelial tissues is the transmembrane protein, E-cadherin, found at the surface of epithelial cells. Though originally investigated for its essential role in mediating intercellular cohesion, its impact on a wide array of physiological processes underscores its fundamental contributions to tissue development and its perturbation in a variety of common diseases.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"189-99"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.854778","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31846226","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 58
Leaders in cell adhesion: an interview with Richard Hynes, pioneer of cell-matrix interactions. Interview by Pamela Cowin. 细胞粘附的领导者:采访细胞-基质相互作用的先驱理查德·海因斯。帕梅拉·考文采访。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-25 DOI: 10.3109/15419061.2013.857662
Richard Hynes
{"title":"Leaders in cell adhesion: an interview with Richard Hynes, pioneer of cell-matrix interactions. Interview by Pamela Cowin.","authors":"Richard Hynes","doi":"10.3109/15419061.2013.857662","DOIUrl":"https://doi.org/10.3109/15419061.2013.857662","url":null,"abstract":"<p><p>On a recent visit Richard O Hynes, FRS, HHMI, Daniel K. Ludwig Professor for Cancer Research at the Koch Institute for Integrative Cancer Research, MIT, graciously agreed to be interviewed in person for the first in Cell Communication and Adhesion's series on \"Leaders in Cell Adhesion\". In this interview we discussed three things: 1) the early role of family, mentors, and luck on his career path; 2) his major discoveries of fibronectin, integrins and the evolution of extracellular matrix proteins; and 3) his role in, and thoughts on, current science policy. This interview reveals his characteristic calmness and infectious optimism, his spontaneous and down to earth sense of humor, and his great ability to place scientific questions in perspective. The interview, carried out on April 30(th) 2013 is reported here verbatim with only minor editing for clarity.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"139-46"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.857662","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31900739","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Highlighting young investigators: guest editor Ramanuj DasGupta. Ram DasGupta: pushing the boundaries of β-catenin signaling and drug development. 特邀编辑拉马努杰·达斯古普塔(Ramanuj DasGupta)。Ram DasGupta:推动β-连环蛋白信号和药物开发的边界。
Cell Communication and Adhesion Pub Date : 2013-12-01 Epub Date: 2013-11-25 DOI: 10.3109/15419061.2013.858134
Pamela Cowin
{"title":"Highlighting young investigators: guest editor Ramanuj DasGupta. Ram DasGupta: pushing the boundaries of β-catenin signaling and drug development.","authors":"Pamela Cowin","doi":"10.3109/15419061.2013.858134","DOIUrl":"https://doi.org/10.3109/15419061.2013.858134","url":null,"abstract":"<p><p>From generating the TOP-GAL mouse to pioneering high-throughput RNAi, and small molecule chemical genetic screens in Drosophila and mammalian cells, Ram DasGupta has consistently developed innovative technological tools of immense value to the fields in which he has chosen to work.</p>","PeriodicalId":55269,"journal":{"name":"Cell Communication and Adhesion","volume":"20 6","pages":"151-3"},"PeriodicalIF":0.0,"publicationDate":"2013-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.3109/15419061.2013.858134","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"31900738","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
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