Identification and functional characterization of two type VI collagen receptors, alpha 3 beta 1 integrin and NG2, during avian corneal stromal development

The development and maintenance of extracellular matrix architecture in the corneal stroma is associated with abundant type VI collagen deposition. This collagen has been implicated in mediating both cell-matrix and matrix-matrix interactions. Although corneal fibroblasts spread extensively on this...

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Veröffentlicht in:Investigative ophthalmology & visual science 1998-02, Vol.39 (2), p.263-275
Hauptverfasser: Doane, KJ, Howell, SJ, Birk, DE
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description The development and maintenance of extracellular matrix architecture in the corneal stroma is associated with abundant type VI collagen deposition. This collagen has been implicated in mediating both cell-matrix and matrix-matrix interactions. Although corneal fibroblasts spread extensively on this collagen, its role in corneal development has not been elucidated. To clarify the role of this collagen, two type VI collagen receptors were studied during corneal development using immunochemical techniques: alpha 3 beta 1 integrin and an integral membrane proteoglycan, NG2. At embryonic day 6, these receptors were present in a diffuse pattern on cells within the cornea and juxtacorneal regions, indicating a migratory phenotype. At embryonic day 14, when the stroma is fully differentiated, alpha 3 and NG2 were localized in a punctate pattern on a subset of corneal fibroblasts, whereas beta 1 was more ubiquitously expressed. Colocalization of NG2 and type VI collagen indicated that this collagen was present and punctate in its organization was associated with NG2-positive cells. Immunochemical analyses at embryonic days 5 and 14 revealed alpha 3 and beta 1 at 155 kDa and 120 kDa, respectively, and demonstrated that these subunits were interacting to form a heterodimer. NG2 was present with a core protein of 330 kDa and an intact proteoglycan of approximately 600 kDa, and analysis of stromal lysates indicated a chondroitin sulfate-containing proteoglycan. Matrix-receptor cross-linking demonstrated the interaction of beta 1 and NG2 in periocular mesenchyme cells and corneal fibroblasts with type VI collagen, whereas only a subset of cells expressed alpha 3, indicating the presence of another beta 1 integrin. No variations between in vivo and in vitro expression of either alpha 3 beta 1 or NG2 were observed. These data indicate that two receptors for type VI collagen, alpha 3 beta 1 and NG2, are present during corneal stromal development, with a functional interaction of these receptors with type VI collagen. These interactions may play a role in corneal cell migration, development, and maintenance of corneal architecture.
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This collagen has been implicated in mediating both cell-matrix and matrix-matrix interactions. Although corneal fibroblasts spread extensively on this collagen, its role in corneal development has not been elucidated. To clarify the role of this collagen, two type VI collagen receptors were studied during corneal development using immunochemical techniques: alpha 3 beta 1 integrin and an integral membrane proteoglycan, NG2. At embryonic day 6, these receptors were present in a diffuse pattern on cells within the cornea and juxtacorneal regions, indicating a migratory phenotype. At embryonic day 14, when the stroma is fully differentiated, alpha 3 and NG2 were localized in a punctate pattern on a subset of corneal fibroblasts, whereas beta 1 was more ubiquitously expressed. Colocalization of NG2 and type VI collagen indicated that this collagen was present and punctate in its organization was associated with NG2-positive cells. Immunochemical analyses at embryonic days 5 and 14 revealed alpha 3 and beta 1 at 155 kDa and 120 kDa, respectively, and demonstrated that these subunits were interacting to form a heterodimer. NG2 was present with a core protein of 330 kDa and an intact proteoglycan of approximately 600 kDa, and analysis of stromal lysates indicated a chondroitin sulfate-containing proteoglycan. Matrix-receptor cross-linking demonstrated the interaction of beta 1 and NG2 in periocular mesenchyme cells and corneal fibroblasts with type VI collagen, whereas only a subset of cells expressed alpha 3, indicating the presence of another beta 1 integrin. No variations between in vivo and in vitro expression of either alpha 3 beta 1 or NG2 were observed. These data indicate that two receptors for type VI collagen, alpha 3 beta 1 and NG2, are present during corneal stromal development, with a functional interaction of these receptors with type VI collagen. 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This collagen has been implicated in mediating both cell-matrix and matrix-matrix interactions. Although corneal fibroblasts spread extensively on this collagen, its role in corneal development has not been elucidated. To clarify the role of this collagen, two type VI collagen receptors were studied during corneal development using immunochemical techniques: alpha 3 beta 1 integrin and an integral membrane proteoglycan, NG2. At embryonic day 6, these receptors were present in a diffuse pattern on cells within the cornea and juxtacorneal regions, indicating a migratory phenotype. At embryonic day 14, when the stroma is fully differentiated, alpha 3 and NG2 were localized in a punctate pattern on a subset of corneal fibroblasts, whereas beta 1 was more ubiquitously expressed. Colocalization of NG2 and type VI collagen indicated that this collagen was present and punctate in its organization was associated with NG2-positive cells. Immunochemical analyses at embryonic days 5 and 14 revealed alpha 3 and beta 1 at 155 kDa and 120 kDa, respectively, and demonstrated that these subunits were interacting to form a heterodimer. NG2 was present with a core protein of 330 kDa and an intact proteoglycan of approximately 600 kDa, and analysis of stromal lysates indicated a chondroitin sulfate-containing proteoglycan. Matrix-receptor cross-linking demonstrated the interaction of beta 1 and NG2 in periocular mesenchyme cells and corneal fibroblasts with type VI collagen, whereas only a subset of cells expressed alpha 3, indicating the presence of another beta 1 integrin. No variations between in vivo and in vitro expression of either alpha 3 beta 1 or NG2 were observed. These data indicate that two receptors for type VI collagen, alpha 3 beta 1 and NG2, are present during corneal stromal development, with a functional interaction of these receptors with type VI collagen. These interactions may play a role in corneal cell migration, development, and maintenance of corneal architecture.</description><subject>Animals</subject><subject>Antigens - metabolism</subject><subject>Cell Culture Techniques</subject><subject>Cell Movement - physiology</subject><subject>Cell Polarity - physiology</subject><subject>Cell Size - physiology</subject><subject>Chick Embryo</subject><subject>Collagen - metabolism</subject><subject>Corneal Stroma - embryology</subject><subject>Corneal Stroma - metabolism</subject><subject>Extracellular Matrix - metabolism</subject><subject>Fibroblasts - metabolism</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Immunoblotting</subject><subject>Integrin alpha3beta1</subject><subject>Integrins - metabolism</subject><subject>Proteoglycans - metabolism</subject><subject>Receptors, Laminin - metabolism</subject><issn>0146-0404</issn><issn>1552-5783</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNotUE1r3DAUNKUl3ab9CQFd2lMM-lrbOpbQJgshuYRezbP0tFawJVeSY9K_kj8bld3TMMww7818qHZsv-f1vu3Ex2pHmWxqKqn8XH1J6ZlSzhinF9WFkm2rOr6r3g4GfXbWacgueALeELt6_Z_ARPQIEXTG6P6d9GBJ3gLJrwuSPweiwzTBET2JqHHJIaZrAtMyAhFkwAyEEeczHqM7RT_c8mti1kKPBF4c-JIQPZZLKccwFzT4glNY5vLV1-qThSnhtzNeVk-_fz3d3NX3j7eHm5_39dgJXvO9pKCV1qyRzDRDAcMpR2oHhK6x0iirWik6sINlIKURFBpsjELNsbXisvpxil1i-Ltiyv3sksZSzGNYU9-qRrVCsmK8OhvXYUbTL9HNEF_785hF_37SR3ccNxexT6XRVNys37ZNqJ73vBHiHXehgXg</recordid><startdate>19980201</startdate><enddate>19980201</enddate><creator>Doane, KJ</creator><creator>Howell, SJ</creator><creator>Birk, DE</creator><general>ARVO</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>19980201</creationdate><title>Identification and functional characterization of two type VI collagen receptors, alpha 3 beta 1 integrin and NG2, during avian corneal stromal development</title><author>Doane, KJ ; Howell, SJ ; Birk, DE</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-h832-2540ac9cc1641d6b164d202e0fbea86f4d9f97438afbf1a44d30a6e6d9ec2e7f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Animals</topic><topic>Antigens - metabolism</topic><topic>Cell Culture Techniques</topic><topic>Cell Movement - physiology</topic><topic>Cell Polarity - physiology</topic><topic>Cell Size - physiology</topic><topic>Chick Embryo</topic><topic>Collagen - metabolism</topic><topic>Corneal Stroma - embryology</topic><topic>Corneal Stroma - metabolism</topic><topic>Extracellular Matrix - metabolism</topic><topic>Fibroblasts - metabolism</topic><topic>Fluorescent Antibody Technique, Indirect</topic><topic>Immunoblotting</topic><topic>Integrin alpha3beta1</topic><topic>Integrins - metabolism</topic><topic>Proteoglycans - metabolism</topic><topic>Receptors, Laminin - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Doane, KJ</creatorcontrib><creatorcontrib>Howell, SJ</creatorcontrib><creatorcontrib>Birk, DE</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative ophthalmology &amp; visual science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Doane, KJ</au><au>Howell, SJ</au><au>Birk, DE</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification and functional characterization of two type VI collagen receptors, alpha 3 beta 1 integrin and NG2, during avian corneal stromal development</atitle><jtitle>Investigative ophthalmology &amp; visual science</jtitle><addtitle>Invest Ophthalmol Vis Sci</addtitle><date>1998-02-01</date><risdate>1998</risdate><volume>39</volume><issue>2</issue><spage>263</spage><epage>275</epage><pages>263-275</pages><issn>0146-0404</issn><eissn>1552-5783</eissn><abstract>The development and maintenance of extracellular matrix architecture in the corneal stroma is associated with abundant type VI collagen deposition. This collagen has been implicated in mediating both cell-matrix and matrix-matrix interactions. Although corneal fibroblasts spread extensively on this collagen, its role in corneal development has not been elucidated. To clarify the role of this collagen, two type VI collagen receptors were studied during corneal development using immunochemical techniques: alpha 3 beta 1 integrin and an integral membrane proteoglycan, NG2. At embryonic day 6, these receptors were present in a diffuse pattern on cells within the cornea and juxtacorneal regions, indicating a migratory phenotype. At embryonic day 14, when the stroma is fully differentiated, alpha 3 and NG2 were localized in a punctate pattern on a subset of corneal fibroblasts, whereas beta 1 was more ubiquitously expressed. Colocalization of NG2 and type VI collagen indicated that this collagen was present and punctate in its organization was associated with NG2-positive cells. Immunochemical analyses at embryonic days 5 and 14 revealed alpha 3 and beta 1 at 155 kDa and 120 kDa, respectively, and demonstrated that these subunits were interacting to form a heterodimer. NG2 was present with a core protein of 330 kDa and an intact proteoglycan of approximately 600 kDa, and analysis of stromal lysates indicated a chondroitin sulfate-containing proteoglycan. Matrix-receptor cross-linking demonstrated the interaction of beta 1 and NG2 in periocular mesenchyme cells and corneal fibroblasts with type VI collagen, whereas only a subset of cells expressed alpha 3, indicating the presence of another beta 1 integrin. No variations between in vivo and in vitro expression of either alpha 3 beta 1 or NG2 were observed. These data indicate that two receptors for type VI collagen, alpha 3 beta 1 and NG2, are present during corneal stromal development, with a functional interaction of these receptors with type VI collagen. These interactions may play a role in corneal cell migration, development, and maintenance of corneal architecture.</abstract><cop>United States</cop><pub>ARVO</pub><pmid>9477982</pmid><tpages>13</tpages></addata></record>
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source MEDLINE; EZB-FREE-00999 freely available EZB journals
subjects Animals
Antigens - metabolism
Cell Culture Techniques
Cell Movement - physiology
Cell Polarity - physiology
Cell Size - physiology
Chick Embryo
Collagen - metabolism
Corneal Stroma - embryology
Corneal Stroma - metabolism
Extracellular Matrix - metabolism
Fibroblasts - metabolism
Fluorescent Antibody Technique, Indirect
Immunoblotting
Integrin alpha3beta1
Integrins - metabolism
Proteoglycans - metabolism
Receptors, Laminin - metabolism
title Identification and functional characterization of two type VI collagen receptors, alpha 3 beta 1 integrin and NG2, during avian corneal stromal development
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