The extracellular matrix of the dermis: flexible structures with dynamic functions
: The current understanding of the role of extracellular matrix proteins is mainly based on their structural properties and their assembly into complex networks. The multiplicity of interactions between cells, cytokines and growth factors within the networks determines functional units dictating th...
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Veröffentlicht in: | Experimental dermatology 2011-08, Vol.20 (8), p.689-695 |
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description | : The current understanding of the role of extracellular matrix proteins is mainly based on their structural properties and their assembly into complex networks. The multiplicity of interactions between cells, cytokines and growth factors within the networks determines functional units dictating the biophysical properties of tissues. This review focuses on the understanding how alterations in the genes, modifying enzymes or biological functions of extracellular matrix molecules, lead to inborn or acquired skin disorders. Analysis of the disease mechanisms provides the basis for the emerging concept that not solely structural defects of single extracellular matrix proteins are at fault, but rather that the functional unit as a whole is not working properly, causing similar clinical symptoms although the causative genes are entirely different. The understanding of these disease‐causing pathways has already led to surprising new therapeutic developments applied to rare inborn disorders. They now permit to design new concepts for the treatment of more common diseases associated with the accumulation of connective tissue and alterations of the biomechanical properties of the extracellular matrix. |
doi_str_mv | 10.1111/j.1600-0625.2011.01313.x |
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The multiplicity of interactions between cells, cytokines and growth factors within the networks determines functional units dictating the biophysical properties of tissues. This review focuses on the understanding how alterations in the genes, modifying enzymes or biological functions of extracellular matrix molecules, lead to inborn or acquired skin disorders. Analysis of the disease mechanisms provides the basis for the emerging concept that not solely structural defects of single extracellular matrix proteins are at fault, but rather that the functional unit as a whole is not working properly, causing similar clinical symptoms although the causative genes are entirely different. The understanding of these disease‐causing pathways has already led to surprising new therapeutic developments applied to rare inborn disorders. They now permit to design new concepts for the treatment of more common diseases associated with the accumulation of connective tissue and alterations of the biomechanical properties of the extracellular matrix.</description><subject>Biological and medical sciences</subject><subject>Bullous diseases of the skin</subject><subject>collagen</subject><subject>Collagen - physiology</subject><subject>Dermatology</subject><subject>Dermis - physiology</subject><subject>Ehlers-Danlos syndromes</subject><subject>Extracellular Matrix - physiology</subject><subject>Extracellular Matrix Proteins - physiology</subject><subject>fibrillin</subject><subject>fibrillogenesis</subject><subject>Humans</subject><subject>integrins</subject><subject>laminin</subject><subject>Marfan syndrome</subject><subject>Medical sciences</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Signal Transduction - physiology</subject><subject>skin blistering diseases</subject><subject>Skin Diseases - physiopathology</subject><subject>TGF-β</subject><issn>0906-6705</issn><issn>1600-0625</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkV9v0zAUxS0EYmXwFZBfEE_JruvGdpB4QGWMwcQ_FdE3y3GvNZck3WxHS789Di3FL7Z0fse69xxCKIOS5XOxLZkAKEDMq3IOjJXAOOPl-IjMTsJjMoMaRCEkVGfkWYxbACa5rJ6SszkTrKoYm5Efq1ukOKZgLLbt0JpAO5OCH-nO0ZS1DYbOxzfUtTj6pkUaUxhsGgJG-uDTLd3se9N5S93Q2-R3fXxOnjjTRnxxvM_Jzw-Xq-XH4ubr1fXy3U1hF1zyoqrB1a5qDDc1V7iohFKc1VY0NQqrYCOl4garvFpjDGAjHBfGoXJWsEYCPyevD__ehd39gDHpPOi0helxN0StpFALqRjL5MsjOTQdbvRd8J0Je_0vhgy8OgImWtO6YHrr438uDwwSRObeHrgH3-L-pDPQUy16q6f09ZS-nmrRf2vRo75cv59e2V8c_D4mHE9-E35rMVWjf3250t--L9Wn9ee1XvE_9iePpA</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Krieg, Thomas</creator><creator>Aumailley, Monique</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201108</creationdate><title>The extracellular matrix of the dermis: flexible structures with dynamic functions</title><author>Krieg, Thomas ; Aumailley, Monique</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4373-590f9f5ba3a938e45688319c6b9e6c80d7783ae5013baa0eb6f36afe8fc61b703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Biological and medical sciences</topic><topic>Bullous diseases of the skin</topic><topic>collagen</topic><topic>Collagen - physiology</topic><topic>Dermatology</topic><topic>Dermis - physiology</topic><topic>Ehlers-Danlos syndromes</topic><topic>Extracellular Matrix - physiology</topic><topic>Extracellular Matrix Proteins - physiology</topic><topic>fibrillin</topic><topic>fibrillogenesis</topic><topic>Humans</topic><topic>integrins</topic><topic>laminin</topic><topic>Marfan syndrome</topic><topic>Medical sciences</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Signal Transduction - physiology</topic><topic>skin blistering diseases</topic><topic>Skin Diseases - physiopathology</topic><topic>TGF-β</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krieg, Thomas</creatorcontrib><creatorcontrib>Aumailley, Monique</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krieg, Thomas</au><au>Aumailley, Monique</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The extracellular matrix of the dermis: flexible structures with dynamic functions</atitle><jtitle>Experimental dermatology</jtitle><addtitle>Exp Dermatol</addtitle><date>2011-08</date><risdate>2011</risdate><volume>20</volume><issue>8</issue><spage>689</spage><epage>695</epage><pages>689-695</pages><issn>0906-6705</issn><eissn>1600-0625</eissn><abstract>: The current understanding of the role of extracellular matrix proteins is mainly based on their structural properties and their assembly into complex networks. The multiplicity of interactions between cells, cytokines and growth factors within the networks determines functional units dictating the biophysical properties of tissues. This review focuses on the understanding how alterations in the genes, modifying enzymes or biological functions of extracellular matrix molecules, lead to inborn or acquired skin disorders. Analysis of the disease mechanisms provides the basis for the emerging concept that not solely structural defects of single extracellular matrix proteins are at fault, but rather that the functional unit as a whole is not working properly, causing similar clinical symptoms although the causative genes are entirely different. The understanding of these disease‐causing pathways has already led to surprising new therapeutic developments applied to rare inborn disorders. 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subjects | Biological and medical sciences Bullous diseases of the skin collagen Collagen - physiology Dermatology Dermis - physiology Ehlers-Danlos syndromes Extracellular Matrix - physiology Extracellular Matrix Proteins - physiology fibrillin fibrillogenesis Humans integrins laminin Marfan syndrome Medical sciences Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Signal Transduction - physiology skin blistering diseases Skin Diseases - physiopathology TGF-β |
title | The extracellular matrix of the dermis: flexible structures with dynamic functions |
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