Increased Dermal Expression of Platelet-Derived Growth Factor Receptors in Growth-Activated Skin Wounds and Psoriasis
Platelet-derived growth factor (PDGF) is a potent mitogenic and chemotactic factor for fibroblasts and other cell types. PDGF effects are mediated by binding of PDGF to dimeric PDGF receptors possessing intrinsic tyrosine kinase activity. We examined the expression pattern of PDGF receptors in cryos...
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Veröffentlicht in: | Journal of investigative dermatology 1991-06, Vol.96 (6), p.983-986 |
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creator | Krane, Jeffrey F. Murphy, Daniel P. Gottlieb, Alice B. Carter, D Martin Hart, Charles E. Krueger, James G. |
description | Platelet-derived growth factor (PDGF) is a potent mitogenic and chemotactic factor for fibroblasts and other cell types. PDGF effects are mediated by binding of PDGF to dimeric PDGF receptors possessing intrinsic tyrosine kinase activity. We examined the expression pattern of PDGF receptors in cryostat sections of normal and growth-activated human skin using a monoclonal antibody, PR7212, specific for the β subunit of the PDGF receptor. PDGF receptors were expressed at low levels in normal skin, with only occasional staining oldermal connective tissue cells. In contrast, PDGF receptor expression was greatly elevated in the dermis of growth-activated skin from 15 chronic wounds and 10 psoriatic lesions. PDGF receptors were increased in dermal fibroblasts and in dermal blood vessels in both conditions. Immunoblot analysis confirmed the increased expression of β-subtype PDGF receptors in psoriatic lesional tissue. PDGF receptors were not detected in normal or growth-activated epidermis. Differential expression of PDGF receptors could regulate increased proliferation of vascular and connective tissue cells observed in psoriasis and chronic wounds. |
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PDGF effects are mediated by binding of PDGF to dimeric PDGF receptors possessing intrinsic tyrosine kinase activity. We examined the expression pattern of PDGF receptors in cryostat sections of normal and growth-activated human skin using a monoclonal antibody, PR7212, specific for the β subunit of the PDGF receptor. PDGF receptors were expressed at low levels in normal skin, with only occasional staining oldermal connective tissue cells. In contrast, PDGF receptor expression was greatly elevated in the dermis of growth-activated skin from 15 chronic wounds and 10 psoriatic lesions. PDGF receptors were increased in dermal fibroblasts and in dermal blood vessels in both conditions. Immunoblot analysis confirmed the increased expression of β-subtype PDGF receptors in psoriatic lesional tissue. PDGF receptors were not detected in normal or growth-activated epidermis. Differential expression of PDGF receptors could regulate increased proliferation of vascular and connective tissue cells observed in psoriasis and chronic wounds.</description><identifier>ISSN: 0022-202X</identifier><identifier>EISSN: 1523-1747</identifier><identifier>DOI: 10.1111/1523-1747.ep12476485</identifier><identifier>PMID: 1646268</identifier><identifier>CODEN: JIDEAE</identifier><language>eng</language><publisher>Danvers, MA: Elsevier Inc</publisher><subject>Antibodies, Monoclonal ; Biological and medical sciences ; Blood vessels ; Blotting, Western ; Cell proliferation ; Chemotactic factors ; Connective tissues ; Dermatology ; Dermis ; Epidermis ; Fibroblasts ; Humans ; Immunohistochemistry ; Medical sciences ; Monoclonal antibodies ; Platelet-Derived Growth Factor ; Platelet-derived growth factor receptors ; Protein-tyrosine kinase ; Psoriasis ; Psoriasis - metabolism ; Psoriasis. Parapsoriasis. Lichen ; Receptors, Cell Surface - metabolism ; Receptors, Platelet-Derived Growth Factor ; Skin ; Skin - injuries ; Skin - metabolism ; Wounds ; Wounds and Injuries - metabolism</subject><ispartof>Journal of investigative dermatology, 1991-06, Vol.96 (6), p.983-986</ispartof><rights>1991 The Society for Investigative Dermatology, Inc</rights><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c485t-e86cd17f184e73b7c0a11297b6928c5a8abdb6cc3d16e9ce0b8b81f1e0babefc3</citedby><cites>FETCH-LOGICAL-c485t-e86cd17f184e73b7c0a11297b6928c5a8abdb6cc3d16e9ce0b8b81f1e0babefc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5038472$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1646268$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Krane, Jeffrey F.</creatorcontrib><creatorcontrib>Murphy, Daniel P.</creatorcontrib><creatorcontrib>Gottlieb, Alice B.</creatorcontrib><creatorcontrib>Carter, D Martin</creatorcontrib><creatorcontrib>Hart, Charles E.</creatorcontrib><creatorcontrib>Krueger, James G.</creatorcontrib><title>Increased Dermal Expression of Platelet-Derived Growth Factor Receptors in Growth-Activated Skin Wounds and Psoriasis</title><title>Journal of investigative dermatology</title><addtitle>J Invest Dermatol</addtitle><description>Platelet-derived growth factor (PDGF) is a potent mitogenic and chemotactic factor for fibroblasts and other cell types. PDGF effects are mediated by binding of PDGF to dimeric PDGF receptors possessing intrinsic tyrosine kinase activity. We examined the expression pattern of PDGF receptors in cryostat sections of normal and growth-activated human skin using a monoclonal antibody, PR7212, specific for the β subunit of the PDGF receptor. PDGF receptors were expressed at low levels in normal skin, with only occasional staining oldermal connective tissue cells. In contrast, PDGF receptor expression was greatly elevated in the dermis of growth-activated skin from 15 chronic wounds and 10 psoriatic lesions. PDGF receptors were increased in dermal fibroblasts and in dermal blood vessels in both conditions. Immunoblot analysis confirmed the increased expression of β-subtype PDGF receptors in psoriatic lesional tissue. PDGF receptors were not detected in normal or growth-activated epidermis. Differential expression of PDGF receptors could regulate increased proliferation of vascular and connective tissue cells observed in psoriasis and chronic wounds.</description><subject>Antibodies, Monoclonal</subject><subject>Biological and medical sciences</subject><subject>Blood vessels</subject><subject>Blotting, Western</subject><subject>Cell proliferation</subject><subject>Chemotactic factors</subject><subject>Connective tissues</subject><subject>Dermatology</subject><subject>Dermis</subject><subject>Epidermis</subject><subject>Fibroblasts</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Medical sciences</subject><subject>Monoclonal antibodies</subject><subject>Platelet-Derived Growth Factor</subject><subject>Platelet-derived growth factor receptors</subject><subject>Protein-tyrosine kinase</subject><subject>Psoriasis</subject><subject>Psoriasis - metabolism</subject><subject>Psoriasis. Parapsoriasis. Lichen</subject><subject>Receptors, Cell Surface - metabolism</subject><subject>Receptors, Platelet-Derived Growth Factor</subject><subject>Skin</subject><subject>Skin - injuries</subject><subject>Skin - metabolism</subject><subject>Wounds</subject><subject>Wounds and Injuries - metabolism</subject><issn>0022-202X</issn><issn>1523-1747</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi0EKkvhH4DkA0JcUmzHcbwXpKq0pVIlKj4EN8sZT4QhG6eeZIF_j1e7am_1ZUbzPq-_XsZeSnEiy3onG1VXstXtCU5S6dZo2zxiq7vxY7YSQqlKCfXjKXtG9EsIaXRjj9hRqUYZu2LL1QgZPWHgHzBv_MDP_04ZiWIaeer5zeBnHHCuihq3hbrM6c_8k194mFPmnxFwKg3xOB6k6hTmuC2uwL_8LtPvaRkDcT8GfkMpR0-RnrMnvR8IXxzqMft2cf717GN1_eny6uz0uoLylrlCayDItpdWY1t3LQgvpVq3nVkrC423vgudAaiDNLgGFJ3trOxlaXyHPdTH7M1-3ymn2wVpdptIgMPgR0wLOSuM0NqaAr59EJTKNsLW0qwLqvco5ESUsXdTjhuf_zkp3C4Yt0vA7RJw98EU26vDCUu3wXBv2idR9NcH3RP4oc9-hEh3WCNqq1tVsPd7DMu3bSNmRxBxBAwxI8wupPjwPf4D9ZCr7Q</recordid><startdate>19910601</startdate><enddate>19910601</enddate><creator>Krane, Jeffrey F.</creator><creator>Murphy, Daniel P.</creator><creator>Gottlieb, Alice B.</creator><creator>Carter, D Martin</creator><creator>Hart, Charles E.</creator><creator>Krueger, James G.</creator><general>Elsevier Inc</general><general>Nature Publishing</general><scope>6I.</scope><scope>AAFTH</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>19910601</creationdate><title>Increased Dermal Expression of Platelet-Derived Growth Factor Receptors in Growth-Activated Skin Wounds and Psoriasis</title><author>Krane, Jeffrey F. ; Murphy, Daniel P. ; Gottlieb, Alice B. ; Carter, D Martin ; Hart, Charles E. ; Krueger, James G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c485t-e86cd17f184e73b7c0a11297b6928c5a8abdb6cc3d16e9ce0b8b81f1e0babefc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Antibodies, Monoclonal</topic><topic>Biological and medical sciences</topic><topic>Blood vessels</topic><topic>Blotting, Western</topic><topic>Cell proliferation</topic><topic>Chemotactic factors</topic><topic>Connective tissues</topic><topic>Dermatology</topic><topic>Dermis</topic><topic>Epidermis</topic><topic>Fibroblasts</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Medical sciences</topic><topic>Monoclonal antibodies</topic><topic>Platelet-Derived Growth Factor</topic><topic>Platelet-derived growth factor receptors</topic><topic>Protein-tyrosine kinase</topic><topic>Psoriasis</topic><topic>Psoriasis - metabolism</topic><topic>Psoriasis. Parapsoriasis. Lichen</topic><topic>Receptors, Cell Surface - metabolism</topic><topic>Receptors, Platelet-Derived Growth Factor</topic><topic>Skin</topic><topic>Skin - injuries</topic><topic>Skin - metabolism</topic><topic>Wounds</topic><topic>Wounds and Injuries - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krane, Jeffrey F.</creatorcontrib><creatorcontrib>Murphy, Daniel P.</creatorcontrib><creatorcontrib>Gottlieb, Alice B.</creatorcontrib><creatorcontrib>Carter, D Martin</creatorcontrib><creatorcontrib>Hart, Charles E.</creatorcontrib><creatorcontrib>Krueger, James G.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of investigative dermatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krane, Jeffrey F.</au><au>Murphy, Daniel P.</au><au>Gottlieb, Alice B.</au><au>Carter, D Martin</au><au>Hart, Charles E.</au><au>Krueger, James G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Increased Dermal Expression of Platelet-Derived Growth Factor Receptors in Growth-Activated Skin Wounds and Psoriasis</atitle><jtitle>Journal of investigative dermatology</jtitle><addtitle>J Invest Dermatol</addtitle><date>1991-06-01</date><risdate>1991</risdate><volume>96</volume><issue>6</issue><spage>983</spage><epage>986</epage><pages>983-986</pages><issn>0022-202X</issn><eissn>1523-1747</eissn><coden>JIDEAE</coden><abstract>Platelet-derived growth factor (PDGF) is a potent mitogenic and chemotactic factor for fibroblasts and other cell types. PDGF effects are mediated by binding of PDGF to dimeric PDGF receptors possessing intrinsic tyrosine kinase activity. We examined the expression pattern of PDGF receptors in cryostat sections of normal and growth-activated human skin using a monoclonal antibody, PR7212, specific for the β subunit of the PDGF receptor. PDGF receptors were expressed at low levels in normal skin, with only occasional staining oldermal connective tissue cells. In contrast, PDGF receptor expression was greatly elevated in the dermis of growth-activated skin from 15 chronic wounds and 10 psoriatic lesions. PDGF receptors were increased in dermal fibroblasts and in dermal blood vessels in both conditions. Immunoblot analysis confirmed the increased expression of β-subtype PDGF receptors in psoriatic lesional tissue. PDGF receptors were not detected in normal or growth-activated epidermis. Differential expression of PDGF receptors could regulate increased proliferation of vascular and connective tissue cells observed in psoriasis and chronic wounds.</abstract><cop>Danvers, MA</cop><pub>Elsevier Inc</pub><pmid>1646268</pmid><doi>10.1111/1523-1747.ep12476485</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies, Monoclonal Biological and medical sciences Blood vessels Blotting, Western Cell proliferation Chemotactic factors Connective tissues Dermatology Dermis Epidermis Fibroblasts Humans Immunohistochemistry Medical sciences Monoclonal antibodies Platelet-Derived Growth Factor Platelet-derived growth factor receptors Protein-tyrosine kinase Psoriasis Psoriasis - metabolism Psoriasis. Parapsoriasis. Lichen Receptors, Cell Surface - metabolism Receptors, Platelet-Derived Growth Factor Skin Skin - injuries Skin - metabolism Wounds Wounds and Injuries - metabolism |
title | Increased Dermal Expression of Platelet-Derived Growth Factor Receptors in Growth-Activated Skin Wounds and Psoriasis |
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