Matrix remodeling in chronic lung diseases
Multicellular organisms synthesize and renew components of their subcellular and scaffolding proteins, collectively known as the extracellular matrix molecules (ECMs). In the lung, ECMs maintain tensile strength, elasticity, and dictate the specialized function of multiple cell lineages. These funct...
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Veröffentlicht in: | Matrix biology 2018-11, Vol.73, p.52-63 |
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description | Multicellular organisms synthesize and renew components of their subcellular and scaffolding proteins, collectively known as the extracellular matrix molecules (ECMs). In the lung, ECMs maintain tensile strength, elasticity, and dictate the specialized function of multiple cell lineages. These functions are critical in lung homeostatic processes including cellular migration and proliferation during morphogenesis or in response to repair. Alterations in lung ECMs that expose cells to new cryptic fragments, generated in response to endogenous proteinases or exogenous toxins, are associated with the development of several common respiratory diseases. How lung ECMs provide or relay vital signals to epithelial and mesenchymal cells has shed new light on development and progression of several common chronic respiratory diseases. This review will consider how ECMs regulate lung homeostasis and their reorganization under pathological conditions that can modulate the inflammatory diseases asthma, chronic obstructive pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF). Better understanding of changes in the distribution of lung ECM could provide novel therapeutic approaches to treat chronic lung diseases.
•The extracellular matrix plays key roles in lung structural integrity, and function.•Proteinases generate cryptic-matrix fragments or “matrikines” that diversify their function.•Fragments of collagen and elastin play pathogenic roles in several common chronic inflammatory lung diseases.•Novel bioengineering approaches utilize photo-crosslinkable elastin-like polypeptides (ELPs) hydrogel to seal injured lung. |
doi_str_mv | 10.1016/j.matbio.2018.03.012 |
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•The extracellular matrix plays key roles in lung structural integrity, and function.•Proteinases generate cryptic-matrix fragments or “matrikines” that diversify their function.•Fragments of collagen and elastin play pathogenic roles in several common chronic inflammatory lung diseases.•Novel bioengineering approaches utilize photo-crosslinkable elastin-like polypeptides (ELPs) hydrogel to seal injured lung.</description><identifier>ISSN: 0945-053X</identifier><identifier>EISSN: 1569-1802</identifier><identifier>DOI: 10.1016/j.matbio.2018.03.012</identifier><identifier>PMID: 29559389</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Asthma ; Cell Movement ; Cell Proliferation ; Cellular biology ; Chronic obstructive pulmonary disease ; Disease Progression ; Extracellular matrix ; Extracellular Matrix - metabolism ; Extracellular Matrix Proteins - metabolism ; Fibrosis ; Homeostasis ; Humans ; Inflammatory diseases ; Lung - metabolism ; Lung - pathology ; Lung diseases ; Lung Diseases - metabolism ; Lung Diseases - pathology ; Mesenchyme ; Molecular biology ; Morphogenesis ; Obstructive lung disease ; Respiratory diseases</subject><ispartof>Matrix biology, 2018-11, Vol.73, p.52-63</ispartof><rights>2018 International Society of Matrix Biology</rights><rights>Copyright © 2018 International Society of Matrix Biology. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Nov 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-ad4eae0af75c2408b80613f1fa17981ff1ecbf69d2fac674d4336ee9553edd6f3</citedby><cites>FETCH-LOGICAL-c491t-ad4eae0af75c2408b80613f1fa17981ff1ecbf69d2fac674d4336ee9553edd6f3</cites><orcidid>0000-0001-9729-1016</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.matbio.2018.03.012$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3548,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29559389$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gu, Bon-Hee</creatorcontrib><creatorcontrib>Madison, Matthew C.</creatorcontrib><creatorcontrib>Corry, David</creatorcontrib><creatorcontrib>Kheradmand, Farrah</creatorcontrib><title>Matrix remodeling in chronic lung diseases</title><title>Matrix biology</title><addtitle>Matrix Biol</addtitle><description>Multicellular organisms synthesize and renew components of their subcellular and scaffolding proteins, collectively known as the extracellular matrix molecules (ECMs). In the lung, ECMs maintain tensile strength, elasticity, and dictate the specialized function of multiple cell lineages. These functions are critical in lung homeostatic processes including cellular migration and proliferation during morphogenesis or in response to repair. Alterations in lung ECMs that expose cells to new cryptic fragments, generated in response to endogenous proteinases or exogenous toxins, are associated with the development of several common respiratory diseases. How lung ECMs provide or relay vital signals to epithelial and mesenchymal cells has shed new light on development and progression of several common chronic respiratory diseases. This review will consider how ECMs regulate lung homeostasis and their reorganization under pathological conditions that can modulate the inflammatory diseases asthma, chronic obstructive pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF). Better understanding of changes in the distribution of lung ECM could provide novel therapeutic approaches to treat chronic lung diseases.
•The extracellular matrix plays key roles in lung structural integrity, and function.•Proteinases generate cryptic-matrix fragments or “matrikines” that diversify their function.•Fragments of collagen and elastin play pathogenic roles in several common chronic inflammatory lung diseases.•Novel bioengineering approaches utilize photo-crosslinkable elastin-like polypeptides (ELPs) hydrogel to seal injured lung.</description><subject>Asthma</subject><subject>Cell Movement</subject><subject>Cell Proliferation</subject><subject>Cellular biology</subject><subject>Chronic obstructive pulmonary disease</subject><subject>Disease Progression</subject><subject>Extracellular matrix</subject><subject>Extracellular Matrix - metabolism</subject><subject>Extracellular Matrix Proteins - metabolism</subject><subject>Fibrosis</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Inflammatory diseases</subject><subject>Lung - metabolism</subject><subject>Lung - pathology</subject><subject>Lung diseases</subject><subject>Lung Diseases - metabolism</subject><subject>Lung Diseases - pathology</subject><subject>Mesenchyme</subject><subject>Molecular biology</subject><subject>Morphogenesis</subject><subject>Obstructive lung disease</subject><subject>Respiratory diseases</subject><issn>0945-053X</issn><issn>1569-1802</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UV1rFTEQDaLY2-o_ELngixR2ndl87OZFKMUvqPii4FvITSZtLrubmuwW_fem3Fo_HnwahjlzZs45jD1DaBFQvdq3k112MbUd4NACbwG7B2yDUukGB-gesg1oIRuQ_OsROy5lDwBC9MNjdtRpKTUf9IadfrRLjt-3mabkaYzz5TbOW3eV0xzddlxr72MhW6g8YY-CHQs9vasn7MvbN5_P3zcXn959OD-7aJzQuDTWC7IENvTSdQKG3QAKecBgsdcDhoDkdkFp3wXrVC-84FwR1Y84ea8CP2GvD7zX624i72hesh3NdY6TzT9MstH8PZnjlblMN0ahQC6hEry8I8jp20plMVMsjsbRzpTWYqphSvIehazQF_9A92nNc5VnOpSiByV6XVHigHI5lZIp3D-DYG7DMHtzCOOWezDATQ2jrj3_U8j90i_3fyulaudNpGyKizQ78jGTW4xP8f8XfgKDdZ00</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Gu, Bon-Hee</creator><creator>Madison, Matthew C.</creator><creator>Corry, David</creator><creator>Kheradmand, Farrah</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><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><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9729-1016</orcidid></search><sort><creationdate>20181101</creationdate><title>Matrix remodeling in chronic lung diseases</title><author>Gu, Bon-Hee ; Madison, Matthew C. ; Corry, David ; Kheradmand, Farrah</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-ad4eae0af75c2408b80613f1fa17981ff1ecbf69d2fac674d4336ee9553edd6f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Asthma</topic><topic>Cell Movement</topic><topic>Cell Proliferation</topic><topic>Cellular biology</topic><topic>Chronic obstructive pulmonary disease</topic><topic>Disease Progression</topic><topic>Extracellular matrix</topic><topic>Extracellular Matrix - metabolism</topic><topic>Extracellular Matrix Proteins - metabolism</topic><topic>Fibrosis</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Inflammatory diseases</topic><topic>Lung - metabolism</topic><topic>Lung - pathology</topic><topic>Lung diseases</topic><topic>Lung Diseases - metabolism</topic><topic>Lung Diseases - pathology</topic><topic>Mesenchyme</topic><topic>Molecular biology</topic><topic>Morphogenesis</topic><topic>Obstructive lung disease</topic><topic>Respiratory diseases</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Bon-Hee</creatorcontrib><creatorcontrib>Madison, Matthew C.</creatorcontrib><creatorcontrib>Corry, David</creatorcontrib><creatorcontrib>Kheradmand, Farrah</creatorcontrib><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>Matrix biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Bon-Hee</au><au>Madison, Matthew C.</au><au>Corry, David</au><au>Kheradmand, Farrah</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Matrix remodeling in chronic lung diseases</atitle><jtitle>Matrix biology</jtitle><addtitle>Matrix Biol</addtitle><date>2018-11-01</date><risdate>2018</risdate><volume>73</volume><spage>52</spage><epage>63</epage><pages>52-63</pages><issn>0945-053X</issn><eissn>1569-1802</eissn><abstract>Multicellular organisms synthesize and renew components of their subcellular and scaffolding proteins, collectively known as the extracellular matrix molecules (ECMs). In the lung, ECMs maintain tensile strength, elasticity, and dictate the specialized function of multiple cell lineages. These functions are critical in lung homeostatic processes including cellular migration and proliferation during morphogenesis or in response to repair. Alterations in lung ECMs that expose cells to new cryptic fragments, generated in response to endogenous proteinases or exogenous toxins, are associated with the development of several common respiratory diseases. How lung ECMs provide or relay vital signals to epithelial and mesenchymal cells has shed new light on development and progression of several common chronic respiratory diseases. This review will consider how ECMs regulate lung homeostasis and their reorganization under pathological conditions that can modulate the inflammatory diseases asthma, chronic obstructive pulmonary disease (COPD), and idiopathic pulmonary fibrosis (IPF). Better understanding of changes in the distribution of lung ECM could provide novel therapeutic approaches to treat chronic lung diseases.
•The extracellular matrix plays key roles in lung structural integrity, and function.•Proteinases generate cryptic-matrix fragments or “matrikines” that diversify their function.•Fragments of collagen and elastin play pathogenic roles in several common chronic inflammatory lung diseases.•Novel bioengineering approaches utilize photo-crosslinkable elastin-like polypeptides (ELPs) hydrogel to seal injured lung.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29559389</pmid><doi>10.1016/j.matbio.2018.03.012</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-9729-1016</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Asthma Cell Movement Cell Proliferation Cellular biology Chronic obstructive pulmonary disease Disease Progression Extracellular matrix Extracellular Matrix - metabolism Extracellular Matrix Proteins - metabolism Fibrosis Homeostasis Humans Inflammatory diseases Lung - metabolism Lung - pathology Lung diseases Lung Diseases - metabolism Lung Diseases - pathology Mesenchyme Molecular biology Morphogenesis Obstructive lung disease Respiratory diseases |
title | Matrix remodeling in chronic lung diseases |
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