Potential cellular and molecular causes of hypertrophic scar formation
Abstract A scar is an expected result of wound healing. However, in some individuals, and particularly in burn victims, the wound healing processes may lead to a fibrotic hypertrophic scar, which is raised, red, inflexible and responsible serious functional and cosmetic problems. It seems that a wid...
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Veröffentlicht in: | Burns 2009-02, Vol.35 (1), p.15-29 |
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description | Abstract A scar is an expected result of wound healing. However, in some individuals, and particularly in burn victims, the wound healing processes may lead to a fibrotic hypertrophic scar, which is raised, red, inflexible and responsible serious functional and cosmetic problems. It seems that a wide array of subsequent processes are involved in hypertrophic scar formation, like an affected haemostasis, exaggerated inflammation, prolonged reepithelialization, overabundant extracellular matrix production, augmented neovascularization, atypical extracellular matrix remodeling and reduced apoptosis. Platelets, macrophages, T-lymphocytes, mast cells, Langerhans cells and keratinocytes are directly and indirectly involved in the activation of fibroblasts, which in turn produce excess extracellular matrix. Following the chronology of normal wound healing, we unravel, clarify and reorganize the complex molecular and cellular key processes that may be responsible for hypertrophic scars. It remains unclear whether these processes are a cause or a consequence of unusual scar tissue formation, but raising evidence exists that immunological responses early following wounding play an important role. Therefore, when developing preventive treatment modalities, one should aim to put the early affected wound healing processes back on track as quickly as possible. |
doi_str_mv | 10.1016/j.burns.2008.06.020 |
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However, in some individuals, and particularly in burn victims, the wound healing processes may lead to a fibrotic hypertrophic scar, which is raised, red, inflexible and responsible serious functional and cosmetic problems. It seems that a wide array of subsequent processes are involved in hypertrophic scar formation, like an affected haemostasis, exaggerated inflammation, prolonged reepithelialization, overabundant extracellular matrix production, augmented neovascularization, atypical extracellular matrix remodeling and reduced apoptosis. Platelets, macrophages, T-lymphocytes, mast cells, Langerhans cells and keratinocytes are directly and indirectly involved in the activation of fibroblasts, which in turn produce excess extracellular matrix. Following the chronology of normal wound healing, we unravel, clarify and reorganize the complex molecular and cellular key processes that may be responsible for hypertrophic scars. It remains unclear whether these processes are a cause or a consequence of unusual scar tissue formation, but raising evidence exists that immunological responses early following wounding play an important role. Therefore, when developing preventive treatment modalities, one should aim to put the early affected wound healing processes back on track as quickly as possible.</description><identifier>ISSN: 0305-4179</identifier><identifier>EISSN: 1879-1409</identifier><identifier>DOI: 10.1016/j.burns.2008.06.020</identifier><identifier>PMID: 18952381</identifier><identifier>CODEN: BURND8</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Apoptosis ; Biological and medical sciences ; Burns ; Burns - complications ; Burns - pathology ; Burns - physiopathology ; Cicatrix, Hypertrophic - etiology ; Cicatrix, Hypertrophic - pathology ; Critical Care ; Esthetics ; Extracellular Matrix - pathology ; Female ; Fibrosis ; Humans ; Hypertrophic scar ; Male ; Medical sciences ; Skin ; Skin - pathology ; Skin - physiopathology ; Traumas. Diseases due to physical agents ; Wound healing ; Wound Healing - physiology</subject><ispartof>Burns, 2009-02, Vol.35 (1), p.15-29</ispartof><rights>Elsevier Ltd and ISBI</rights><rights>2008 Elsevier Ltd and ISBI</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-f1dbf63ec7afac5c4260c8bf5d80c70d1119791d2af01b6fe55b221c36c8c7363</citedby><cites>FETCH-LOGICAL-c442t-f1dbf63ec7afac5c4260c8bf5d80c70d1119791d2af01b6fe55b221c36c8c7363</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.burns.2008.06.020$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21096486$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18952381$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van der Veer, Willem M</creatorcontrib><creatorcontrib>Bloemen, Monica C.T</creatorcontrib><creatorcontrib>Ulrich, Magda M.W</creatorcontrib><creatorcontrib>Molema, Grietje</creatorcontrib><creatorcontrib>van Zuijlen, Paul P</creatorcontrib><creatorcontrib>Middelkoop, Esther</creatorcontrib><creatorcontrib>Niessen, Frank B</creatorcontrib><title>Potential cellular and molecular causes of hypertrophic scar formation</title><title>Burns</title><addtitle>Burns</addtitle><description>Abstract A scar is an expected result of wound healing. However, in some individuals, and particularly in burn victims, the wound healing processes may lead to a fibrotic hypertrophic scar, which is raised, red, inflexible and responsible serious functional and cosmetic problems. It seems that a wide array of subsequent processes are involved in hypertrophic scar formation, like an affected haemostasis, exaggerated inflammation, prolonged reepithelialization, overabundant extracellular matrix production, augmented neovascularization, atypical extracellular matrix remodeling and reduced apoptosis. Platelets, macrophages, T-lymphocytes, mast cells, Langerhans cells and keratinocytes are directly and indirectly involved in the activation of fibroblasts, which in turn produce excess extracellular matrix. Following the chronology of normal wound healing, we unravel, clarify and reorganize the complex molecular and cellular key processes that may be responsible for hypertrophic scars. It remains unclear whether these processes are a cause or a consequence of unusual scar tissue formation, but raising evidence exists that immunological responses early following wounding play an important role. Therefore, when developing preventive treatment modalities, one should aim to put the early affected wound healing processes back on track as quickly as possible.</description><subject>Apoptosis</subject><subject>Biological and medical sciences</subject><subject>Burns</subject><subject>Burns - complications</subject><subject>Burns - pathology</subject><subject>Burns - physiopathology</subject><subject>Cicatrix, Hypertrophic - etiology</subject><subject>Cicatrix, Hypertrophic - pathology</subject><subject>Critical Care</subject><subject>Esthetics</subject><subject>Extracellular Matrix - pathology</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Humans</subject><subject>Hypertrophic scar</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Skin</subject><subject>Skin - pathology</subject><subject>Skin - physiopathology</subject><subject>Traumas. Diseases due to physical agents</subject><subject>Wound healing</subject><subject>Wound Healing - physiology</subject><issn>0305-4179</issn><issn>1879-1409</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1r3DAQhkVpaTZJf0Gg-NLe7I5kW5YPLZSQj0KghaZnIY9HRBvb2kp2Yf995ezSQC_RRQg978zwDGMXHAoOXH7aFt0SplgIAFWALEDAK7bhqmlzXkH7mm2ghDqveNOesNMYt5BOreAtO-GqrUWp-IZd__AzTbMzQ4Y0DMtgQmamPhv9QPj0QrNEipm32cN-R2EOfvfgMIuY_qwPo5mdn87ZG2uGSO-O9xn7dX11f3mb332_-Xb59S7HqhJzbnnfWVkSNsYarLESElB1tu4VYAM957xtWt4LY4F30lJdd0JwLCUqbEpZnrGPh7q74H8vFGc9urgObibyS9RSKlAc2gSWBxCDjzGQ1bvgRhP2moNe9emtftKnV30apE76Uur9sfzSjdQ_Z46-EvDhCJgkYLDBTOjiP06k1rJS65yfDxwlGX8cBR3R0YTUu0A46967Fwb58l8eBze51PKR9hS3PiWSZ811FBr0z3XT66JBAYi6qsq_ytKklA</recordid><startdate>20090201</startdate><enddate>20090201</enddate><creator>van der Veer, Willem M</creator><creator>Bloemen, Monica C.T</creator><creator>Ulrich, Magda M.W</creator><creator>Molema, Grietje</creator><creator>van Zuijlen, Paul P</creator><creator>Middelkoop, Esther</creator><creator>Niessen, Frank B</creator><general>Elsevier Ltd</general><general>Elsevier</general><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>7X8</scope></search><sort><creationdate>20090201</creationdate><title>Potential cellular and molecular causes of hypertrophic scar formation</title><author>van der Veer, Willem M ; Bloemen, Monica C.T ; Ulrich, Magda M.W ; Molema, Grietje ; van Zuijlen, Paul P ; Middelkoop, Esther ; Niessen, Frank B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-f1dbf63ec7afac5c4260c8bf5d80c70d1119791d2af01b6fe55b221c36c8c7363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Apoptosis</topic><topic>Biological and medical sciences</topic><topic>Burns</topic><topic>Burns - complications</topic><topic>Burns - pathology</topic><topic>Burns - physiopathology</topic><topic>Cicatrix, Hypertrophic - etiology</topic><topic>Cicatrix, Hypertrophic - pathology</topic><topic>Critical Care</topic><topic>Esthetics</topic><topic>Extracellular Matrix - pathology</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Humans</topic><topic>Hypertrophic scar</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Skin</topic><topic>Skin - pathology</topic><topic>Skin - physiopathology</topic><topic>Traumas. Diseases due to physical agents</topic><topic>Wound healing</topic><topic>Wound Healing - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van der Veer, Willem M</creatorcontrib><creatorcontrib>Bloemen, Monica C.T</creatorcontrib><creatorcontrib>Ulrich, Magda M.W</creatorcontrib><creatorcontrib>Molema, Grietje</creatorcontrib><creatorcontrib>van Zuijlen, Paul P</creatorcontrib><creatorcontrib>Middelkoop, Esther</creatorcontrib><creatorcontrib>Niessen, Frank B</creatorcontrib><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>MEDLINE - Academic</collection><jtitle>Burns</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van der Veer, Willem M</au><au>Bloemen, Monica C.T</au><au>Ulrich, Magda M.W</au><au>Molema, Grietje</au><au>van Zuijlen, Paul P</au><au>Middelkoop, Esther</au><au>Niessen, Frank B</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potential cellular and molecular causes of hypertrophic scar formation</atitle><jtitle>Burns</jtitle><addtitle>Burns</addtitle><date>2009-02-01</date><risdate>2009</risdate><volume>35</volume><issue>1</issue><spage>15</spage><epage>29</epage><pages>15-29</pages><issn>0305-4179</issn><eissn>1879-1409</eissn><coden>BURND8</coden><abstract>Abstract A scar is an expected result of wound healing. However, in some individuals, and particularly in burn victims, the wound healing processes may lead to a fibrotic hypertrophic scar, which is raised, red, inflexible and responsible serious functional and cosmetic problems. It seems that a wide array of subsequent processes are involved in hypertrophic scar formation, like an affected haemostasis, exaggerated inflammation, prolonged reepithelialization, overabundant extracellular matrix production, augmented neovascularization, atypical extracellular matrix remodeling and reduced apoptosis. Platelets, macrophages, T-lymphocytes, mast cells, Langerhans cells and keratinocytes are directly and indirectly involved in the activation of fibroblasts, which in turn produce excess extracellular matrix. Following the chronology of normal wound healing, we unravel, clarify and reorganize the complex molecular and cellular key processes that may be responsible for hypertrophic scars. It remains unclear whether these processes are a cause or a consequence of unusual scar tissue formation, but raising evidence exists that immunological responses early following wounding play an important role. Therefore, when developing preventive treatment modalities, one should aim to put the early affected wound healing processes back on track as quickly as possible.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><pmid>18952381</pmid><doi>10.1016/j.burns.2008.06.020</doi><tpages>15</tpages></addata></record> |
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subjects | Apoptosis Biological and medical sciences Burns Burns - complications Burns - pathology Burns - physiopathology Cicatrix, Hypertrophic - etiology Cicatrix, Hypertrophic - pathology Critical Care Esthetics Extracellular Matrix - pathology Female Fibrosis Humans Hypertrophic scar Male Medical sciences Skin Skin - pathology Skin - physiopathology Traumas. Diseases due to physical agents Wound healing Wound Healing - physiology |
title | Potential cellular and molecular causes of hypertrophic scar formation |
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