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      Biological functions of iduronic acid in chondroitin/dermatan sulfate

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          Abstract

          The presence of iduronic acid in chondroitin/dermatan sulfate changes the properties of the polysaccharides because it generates a more flexible chain with increased binding potentials. Iduronic acid in chondroitin/dermatan sulfate influences multiple cellular properties, such as migration, proliferation, differentiation, angiogenesis and the regulation of cytokine/growth factor activities. Under pathological conditions such as wound healing, inflammation and cancer, iduronic acid has diverse regulatory functions. Iduronic acid is formed by two epimerases (i.e. dermatan sulfate epimerase 1 and 2) that have different tissue distribution and properties. The role of iduronic acid in chondroitin/dermatan sulfate is highlighted by the vast changes in connective tissue features in patients with a new type of Ehler–Danlos syndrome: adducted thumb-clubfoot syndrome. Future research aims to understand the roles of the two epimerases and their interplay with the sulfotransferases involved in chondroitin sulfate/dermatan sulfate biosynthesis. Furthermore, a better definition of chondroitin/dermatan sulfate functions using different knockout models is needed. In this review, we focus on the two enzymes responsible for iduronic acid formation, as well as the role of iduronic acid in health and disease.

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          Most cited references136

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          Negative regulation of transforming growth factor-beta by the proteoglycan decorin.

          Decorin is a small chondroitin-dermatan sulphate proteoglycan consisting of a core protein and a single glycosaminoglycan chain. Eighty per cent of the core protein consists of 10 repeats of a leucin-rich sequence of 24 amino acids. Similar repeats have been found in two other proteoglycans, biglycan and fibromodulin, and in several other proteins including Drosophila morphogenetic proteins. Expression of high levels of decorin in Chinese hamster ovary cells has a dramatic effect on their morphology and growth properties. We now report that this effect is due at least in part to the ability of decorin to bind transforming growth factor-beta, an autocrine factor that stimulates the growth of Chinese hamster ovary cells. As transforming growth factor-beta induces synthesis of decorin in many cell types, our results suggest that decorin may be a component of a feedback system regulating cell growth.
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            Molecular functions of syndecan-1 in disease.

            Syndecan-1 is a cell surface heparan sulfate proteoglycan that binds to many mediators of disease pathogenesis. Through these molecular interactions, syndecan-1 can modulate leukocyte recruitment, cancer cell proliferation and invasion, angiogenesis, microbial attachment and entry, host defense mechanisms, and matrix remodeling. The significance of syndecan-1 interactions in disease is underscored by the striking pathological phenotypes seen in the syndecan-1 null mice when they are challenged with disease-instigating agents or conditions. This review discusses the key molecular functions of syndecan-1 in modulating the onset, progression, and resolution of inflammatory diseases, cancer, and infection. Copyright © 2011 International Society of Matrix Biology. Published by Elsevier B.V. All rights reserved.
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              Versican: a versatile extracellular matrix proteoglycan in cell biology.

              Versican is a large extracellular matrix proteoglycan that is present in a variety of tissues. Successful cloning of the gene in man, mouse, cow and chicken has revealed the existence of at least four splice variants of versican, which differ in the size of the core protein and the number of glycosaminoglycan chains. The highly interactive nature of versican provides a basis for its importance as a structural molecule, creating loose and hydrated matrices during key events in development and disease; and by interacting either directly with cells or indirectly with molecules that associate with cells to, in part, regulate cell adhesion and survival, cell proliferation, cell migration and extracellular matrix assembly. Several studies within the past two years have confirmed a significant role for versican in regulating cell phenotype.
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                Author and article information

                Journal
                FEBS J
                FEBS J
                febs
                The Febs Journal
                Blackwell Publishing Ltd
                1742-464X
                1742-4658
                May 2013
                28 March 2013
                : 280
                : 10
                : 2431-2446
                Affiliations
                Department of Experimental Medical Science, BMC, Lund University Sweden
                Author notes
                A. Malmström, Department of Experimental Medical Science, BMC 12, Lund University, 221 84 Lund, Sweden Fax: +46 462113417 Tel: +46 46 2228574 E-mail: anders.malmstrom@ 123456med.lu.se
                [*]

                Present address Department of Surgical and Morphological Science, University of Insubria, Varese, Italy

                Article
                10.1111/febs.12214
                3717172
                23441919
                de728a9d-d9c0-4a4b-9ad9-16b9849448c7
                Copyright © 2013 Federation of European Biochemical Societies

                Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.

                History
                : 22 December 2012
                : 17 February 2013
                : 18 February 2013
                Categories
                Special Issue

                Molecular biology
                cancer,dermatan sulfate epimerase,dse,dsel,iduronic acid,inflammation,proteoglycans
                Molecular biology
                cancer, dermatan sulfate epimerase, dse, dsel, iduronic acid, inflammation, proteoglycans

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