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      Cytoskeleton in motion: the dynamics of keratin intermediate filaments in epithelia

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          Abstract

          Epithelia are exposed to multiple forms of stress. Keratin intermediate filaments are abundant in epithelia and form cytoskeletal networks that contribute to cell type–specific functions, such as adhesion, migration, and metabolism. A perpetual keratin filament turnover cycle supports these functions. This multistep process keeps the cytoskeleton in motion, facilitating rapid and protein biosynthesis–independent network remodeling while maintaining an intact network. The current challenge is to unravel the molecular mechanisms underlying the regulation of the keratin cycle in relation to actin and microtubule networks and in the context of epithelial tissue function.

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          Most cited references144

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          Transmembrane crosstalk between the extracellular matrix--cytoskeleton crosstalk.

          Integrin-mediated cell adhesions provide dynamic, bidirectional links between the extracellular matrix and the cytoskeleton. Besides having central roles in cell migration and morphogenesis, focal adhesions and related structures convey information across the cell membrane, to regulate extracellular-matrix assembly, cell proliferation, differentiation, and death. This review describes integrin functions, mechanosensors, molecular switches and signal-transduction pathways activated and integrated by adhesion, with a unifying theme being the importance of local physical forces.
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            Dynamic instability of microtubule growth.

            We report here that microtubules in vitro coexist in growing and shrinking populations which interconvert rather infrequently. This dynamic instability is a general property of microtubules and may be fundamental in explaining cellular microtubule organization.
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              Tracking the ends: a dynamic protein network controls the fate of microtubule tips.

              Microtubule plus-end tracking proteins (+TIPs) are a diverse group of evolutionarily conserved cellular factors that accumulate at the ends of growing microtubules. They form dynamic networks through the interaction of a limited set of protein modules, repeat sequences and linear motifs that bind to each other with moderate affinities. +TIPs regulate different aspects of cell architecture by controlling microtubule dynamics, microtubule interactions with cellular structures and signalling factors, and the forces that are exerted on microtubule networks.
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                Author and article information

                Journal
                J Cell Biol
                J. Cell Biol
                jcb
                The Journal of Cell Biology
                The Rockefeller University Press
                0021-9525
                1540-8140
                5 September 2011
                : 194
                : 5
                : 669-678
                Affiliations
                [1 ]Institute of Molecular and Cellular Anatomy, RWTH Aachen University, 52057 Aachen, Germany
                [2 ]Department of Internal Medicine I, University of Ulm, 89081 Ulm, Germany
                [3 ]Division of Cell and Developmental Biology, Translational Centre for Regenerative Medicine Leipzig and Institute of Biology, University of Leipzig, 04103 Leipzig, Germany
                Author notes
                Correspondence to Rudolf Leube: rleube@ 123456ukaachen.de
                Article
                201008095
                10.1083/jcb.201008095
                3171125
                21893596
                691a0a7f-7435-4158-b491-9a98b3151e8b
                © 2011 Windoffer et al.

                This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).

                History
                : 16 August 2010
                : 15 June 2011
                Categories
                Reviews
                Review

                Cell biology
                Cell biology

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