Cell surface receptors for CCN proteins
The CCN family (CYR61; CTGF; NOV; CCN1–6; WISP1–3) of matricellular proteins in mammals is comprised of six homologous members that play important roles in development, inflammation, tissue repair, and a broad range of pathological processes including fibrosis and cancer. Despite considerable effort...
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description | The CCN family (CYR61; CTGF; NOV; CCN1–6; WISP1–3) of matricellular proteins in mammals is comprised of six homologous members that play important roles in development, inflammation, tissue repair, and a broad range of pathological processes including fibrosis and cancer. Despite considerable effort to search for a high affinity CCN-specific receptor akin to growth factor receptors, no such receptor has been found. Rather, CCNs bind several groups of multi-ligand receptors as characteristic of other matricellular proteins. The most extensively documented among CCN-binding receptors are integrins, including α
v
β
3
, α
v
β
5
, α
5
β
1
, α
6
β
1
, α
IIb
β
3
, α
M
β
2
, and α
D
β
2
, which mediate diverse CCN functions in various cell types. CCNs also bind cell surface heparan sulfate proteoglycans (HSPGs), low density liproprotein receptor-related proteins (LRPs), and the cation-independent mannose-6-phosphate (M6P) receptor, which are endocytic receptors that may also serve as co-receptors in cooperation with other cell surface receptors. CCNs have also been reported to bind FGFR-2, Notch, RANK, and TrkA, potentially altering the affinities of these receptors for their ligands. The ability of CCNs to bind a multitude of receptors in various cell types may account for the remarkable versatility of their functions, and underscore the diverse signaling pathways that mediate their activities. |
doi_str_mv | 10.1007/s12079-016-0324-z |
format | Article |
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v
β
3
, α
v
β
5
, α
5
β
1
, α
6
β
1
, α
IIb
β
3
, α
M
β
2
, and α
D
β
2
, which mediate diverse CCN functions in various cell types. CCNs also bind cell surface heparan sulfate proteoglycans (HSPGs), low density liproprotein receptor-related proteins (LRPs), and the cation-independent mannose-6-phosphate (M6P) receptor, which are endocytic receptors that may also serve as co-receptors in cooperation with other cell surface receptors. CCNs have also been reported to bind FGFR-2, Notch, RANK, and TrkA, potentially altering the affinities of these receptors for their ligands. The ability of CCNs to bind a multitude of receptors in various cell types may account for the remarkable versatility of their functions, and underscore the diverse signaling pathways that mediate their activities.</description><identifier>ISSN: 1873-9601</identifier><identifier>EISSN: 1873-961X</identifier><identifier>DOI: 10.1007/s12079-016-0324-z</identifier><identifier>PMID: 27098435</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Biomedical and Life Sciences ; Biomedicine ; Cancer ; CCN proteins ; Cell Biology ; Cell surface ; Connective tissue growth factor ; Cooperativity ; CYR61 protein ; Fibroblast growth factor receptors ; Fibrosis ; Growth factor receptors ; Heparan sulfate ; Heparan sulfate proteoglycans ; Integrins ; Life Sciences ; Mannose ; Matricellular proteins ; Proteins ; Proteoglycans ; Receptor density ; Receptors ; Review ; Signaling ; Sulfates ; TrkA protein</subject><ispartof>Journal of cell communication and signaling, 2016-06, Vol.10 (2), p.121-127</ispartof><rights>The International CCN Society 2016</rights><rights>The International CCN Society</rights><rights>Journal of Cell Communication and Signaling is a copyright of Springer, 2016.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5211-3f54e3daa37973495b7bfe6913206f3ee44e7de8d711c7299d226213b3bb0e7c3</citedby><cites>FETCH-LOGICAL-c5211-3f54e3daa37973495b7bfe6913206f3ee44e7de8d711c7299d226213b3bb0e7c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882306/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC4882306/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,41487,42556,51318,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27098435$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lau, Lester F.</creatorcontrib><title>Cell surface receptors for CCN proteins</title><title>Journal of cell communication and signaling</title><addtitle>J. Cell Commun. Signal</addtitle><addtitle>J Cell Commun Signal</addtitle><description>The CCN family (CYR61; CTGF; NOV; CCN1–6; WISP1–3) of matricellular proteins in mammals is comprised of six homologous members that play important roles in development, inflammation, tissue repair, and a broad range of pathological processes including fibrosis and cancer. Despite considerable effort to search for a high affinity CCN-specific receptor akin to growth factor receptors, no such receptor has been found. Rather, CCNs bind several groups of multi-ligand receptors as characteristic of other matricellular proteins. The most extensively documented among CCN-binding receptors are integrins, including α
v
β
3
, α
v
β
5
, α
5
β
1
, α
6
β
1
, α
IIb
β
3
, α
M
β
2
, and α
D
β
2
, which mediate diverse CCN functions in various cell types. CCNs also bind cell surface heparan sulfate proteoglycans (HSPGs), low density liproprotein receptor-related proteins (LRPs), and the cation-independent mannose-6-phosphate (M6P) receptor, which are endocytic receptors that may also serve as co-receptors in cooperation with other cell surface receptors. CCNs have also been reported to bind FGFR-2, Notch, RANK, and TrkA, potentially altering the affinities of these receptors for their ligands. The ability of CCNs to bind a multitude of receptors in various cell types may account for the remarkable versatility of their functions, and underscore the diverse signaling pathways that mediate their activities.</description><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Cancer</subject><subject>CCN proteins</subject><subject>Cell Biology</subject><subject>Cell surface</subject><subject>Connective tissue growth factor</subject><subject>Cooperativity</subject><subject>CYR61 protein</subject><subject>Fibroblast growth factor receptors</subject><subject>Fibrosis</subject><subject>Growth factor receptors</subject><subject>Heparan sulfate</subject><subject>Heparan sulfate proteoglycans</subject><subject>Integrins</subject><subject>Life Sciences</subject><subject>Mannose</subject><subject>Matricellular proteins</subject><subject>Proteins</subject><subject>Proteoglycans</subject><subject>Receptor density</subject><subject>Receptors</subject><subject>Review</subject><subject>Signaling</subject><subject>Sulfates</subject><subject>TrkA protein</subject><issn>1873-9601</issn><issn>1873-961X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqFUU1LxDAUDKL4sfoDvEjBg16qeUmbNB4ELa4KogcVvIV-vK6VbrMmW0V_vVm6Lqsgnl4emRlm3hCyC_QIKJXHDhiVKqQgQspZFH6ukE1IJA-VgKfVxZvCBtly7oXSWMYM1skGk1QlEY83yUGKTRO4zlZZgYHFAidTY11QGRuk6W0wsWaKdeu2yVqVNQ535nNAHocXD-lVeHN3eZ2e3YSFV4aQV3GEvMwyLpXkkYpzmVcoFHBGRcURowhliUkpAQrJlCoZEwx4zvOcoiz4gJz2upMuH2NZYDu1WaMnth5n9kObrNY_f9r6WY_Mm46ShHEqvMDhXMCa1w7dVI9rV_iQWYumcxqkYlyCEjPo_i_oi-ls6-NpUFHMYxD-SAMCPaqwxjmL1cIMUD2rQfc1aF-DntWgPz1nbznFgvF9dw846QHvdYMf_yvqNL3n50PqN_Bk1pOd57UjtEu-_7T0BRzfowI</recordid><startdate>201606</startdate><enddate>201606</enddate><creator>Lau, Lester F.</creator><general>Springer Netherlands</general><general>John Wiley & Sons, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FH</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201606</creationdate><title>Cell surface receptors for CCN proteins</title><author>Lau, Lester F.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5211-3f54e3daa37973495b7bfe6913206f3ee44e7de8d711c7299d226213b3bb0e7c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Cancer</topic><topic>CCN proteins</topic><topic>Cell Biology</topic><topic>Cell surface</topic><topic>Connective tissue growth factor</topic><topic>Cooperativity</topic><topic>CYR61 protein</topic><topic>Fibroblast growth factor receptors</topic><topic>Fibrosis</topic><topic>Growth factor receptors</topic><topic>Heparan sulfate</topic><topic>Heparan sulfate proteoglycans</topic><topic>Integrins</topic><topic>Life Sciences</topic><topic>Mannose</topic><topic>Matricellular proteins</topic><topic>Proteins</topic><topic>Proteoglycans</topic><topic>Receptor density</topic><topic>Receptors</topic><topic>Review</topic><topic>Signaling</topic><topic>Sulfates</topic><topic>TrkA protein</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lau, Lester F.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of cell communication and signaling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lau, Lester F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cell surface receptors for CCN proteins</atitle><jtitle>Journal of cell communication and signaling</jtitle><stitle>J. Cell Commun. Signal</stitle><addtitle>J Cell Commun Signal</addtitle><date>2016-06</date><risdate>2016</risdate><volume>10</volume><issue>2</issue><spage>121</spage><epage>127</epage><pages>121-127</pages><issn>1873-9601</issn><eissn>1873-961X</eissn><abstract>The CCN family (CYR61; CTGF; NOV; CCN1–6; WISP1–3) of matricellular proteins in mammals is comprised of six homologous members that play important roles in development, inflammation, tissue repair, and a broad range of pathological processes including fibrosis and cancer. Despite considerable effort to search for a high affinity CCN-specific receptor akin to growth factor receptors, no such receptor has been found. Rather, CCNs bind several groups of multi-ligand receptors as characteristic of other matricellular proteins. The most extensively documented among CCN-binding receptors are integrins, including α
v
β
3
, α
v
β
5
, α
5
β
1
, α
6
β
1
, α
IIb
β
3
, α
M
β
2
, and α
D
β
2
, which mediate diverse CCN functions in various cell types. CCNs also bind cell surface heparan sulfate proteoglycans (HSPGs), low density liproprotein receptor-related proteins (LRPs), and the cation-independent mannose-6-phosphate (M6P) receptor, which are endocytic receptors that may also serve as co-receptors in cooperation with other cell surface receptors. CCNs have also been reported to bind FGFR-2, Notch, RANK, and TrkA, potentially altering the affinities of these receptors for their ligands. The ability of CCNs to bind a multitude of receptors in various cell types may account for the remarkable versatility of their functions, and underscore the diverse signaling pathways that mediate their activities.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><pmid>27098435</pmid><doi>10.1007/s12079-016-0324-z</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biomedical and Life Sciences Biomedicine Cancer CCN proteins Cell Biology Cell surface Connective tissue growth factor Cooperativity CYR61 protein Fibroblast growth factor receptors Fibrosis Growth factor receptors Heparan sulfate Heparan sulfate proteoglycans Integrins Life Sciences Mannose Matricellular proteins Proteins Proteoglycans Receptor density Receptors Review Signaling Sulfates TrkA protein |
title | Cell surface receptors for CCN proteins |
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