Trabecular cell expression of fibronectin and MMP-3 is modulated by aqueous humor growth factors
We investigated the mRNA and protein expression of fibronectin and stromelysin-1 (matrix metalloproteinase-3, MMP-3) by trabecular cells treated with growth factors present in primary and secondary aqueous humors. Serum-deprived trabecular cells were incubated for 48 hr or 7 days in medium containin...
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description | We investigated the mRNA and protein expression of fibronectin and stromelysin-1 (matrix metalloproteinase-3, MMP-3) by trabecular cells treated with growth factors present in primary and secondary aqueous humors. Serum-deprived trabecular cells were incubated for 48
hr or 7 days in medium containing either primary or secondary aqueous humor growth factors or in serum-free medium. We extracted total RNA, performed reverse transcription-polymerase chain reaction using primer pairs for fibronectin, stromelysin-1 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and quantified the products. We utilized Western blotting to detect and quantify fibronectin and stromelysin-1 protein. Compared to controls, expression of fibronectin mRNA by trabecular cells was increased by 50 and 100% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 50 and 130% after incubation in secondary aqueous humor growth factors. Stromelysin-1 mRNA expression was decreased by 25 and 50% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 80 and 85% after incubation for 48
hr or 7 days, respectively, in secondary aqueous humor growth factors. Fibronectin protein increased 3·5-fold and 6-fold after incubation for 48
hr with primary or secondary aqueous humor growth factors, respectively; after 7 days, the level increased 4- and 7-folds, respectively. Stromelysin-1 protein was not detectable by western blotting. The up-regulation of fibronectin mRNA by trabecular cells exposed to growth factors present in secondary aqueous humor augmented by the down-regulation of stromelysin-1 mRNA contributed to the accumulation of fibronectin. Our findings open the possibility that induction of stromelysin-1 gene expression in the trabecular meshwork of glaucomatous eyes could effectively reduce buildup of fibronectin in the aqueous outflow pathway to decrease outflow resistance in glaucomatous states of the eye. |
doi_str_mv | 10.1016/j.exer.2003.09.011 |
format | Article |
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hr or 7 days in medium containing either primary or secondary aqueous humor growth factors or in serum-free medium. We extracted total RNA, performed reverse transcription-polymerase chain reaction using primer pairs for fibronectin, stromelysin-1 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and quantified the products. We utilized Western blotting to detect and quantify fibronectin and stromelysin-1 protein. Compared to controls, expression of fibronectin mRNA by trabecular cells was increased by 50 and 100% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 50 and 130% after incubation in secondary aqueous humor growth factors. Stromelysin-1 mRNA expression was decreased by 25 and 50% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 80 and 85% after incubation for 48
hr or 7 days, respectively, in secondary aqueous humor growth factors. Fibronectin protein increased 3·5-fold and 6-fold after incubation for 48
hr with primary or secondary aqueous humor growth factors, respectively; after 7 days, the level increased 4- and 7-folds, respectively. Stromelysin-1 protein was not detectable by western blotting. The up-regulation of fibronectin mRNA by trabecular cells exposed to growth factors present in secondary aqueous humor augmented by the down-regulation of stromelysin-1 mRNA contributed to the accumulation of fibronectin. Our findings open the possibility that induction of stromelysin-1 gene expression in the trabecular meshwork of glaucomatous eyes could effectively reduce buildup of fibronectin in the aqueous outflow pathway to decrease outflow resistance in glaucomatous states of the eye.</description><identifier>ISSN: 0014-4835</identifier><identifier>EISSN: 1096-0007</identifier><identifier>DOI: 10.1016/j.exer.2003.09.011</identifier><identifier>PMID: 15106945</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Animals ; Aqueous Humor - chemistry ; Cells, Cultured ; Culture Media, Serum-Free ; Fibronectins - genetics ; Fibronectins - metabolism ; Gene Expression Regulation - drug effects ; gene therapy ; glaucoma ; Growth Substances - pharmacology ; Matrix Metalloproteinase 3 - genetics ; Matrix Metalloproteinase 3 - metabolism ; primary aqueous humor ; Reverse Transcriptase Polymerase Chain Reaction ; RNA, Messenger - genetics ; secondary aqueous humor ; Swine ; trabecular meshwork ; Trabecular Meshwork - drug effects ; Trabecular Meshwork - metabolism ; western blot</subject><ispartof>Experimental eye research, 2004-03, Vol.78 (3), p.653-660</ispartof><rights>2003 Elsevier Science Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c352t-624e43980e1c7c5575b4876bb5c55e9ef4eaa288120012ddd7583899304a7ca23</citedby><cites>FETCH-LOGICAL-c352t-624e43980e1c7c5575b4876bb5c55e9ef4eaa288120012ddd7583899304a7ca23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S001448350300294X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15106945$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tripathi, Brenda J.</creatorcontrib><creatorcontrib>Tripathi, Ramesh C.</creatorcontrib><creatorcontrib>Chen, Jianguang</creatorcontrib><creatorcontrib>Gotsis, Stelios</creatorcontrib><creatorcontrib>Li, Junping</creatorcontrib><title>Trabecular cell expression of fibronectin and MMP-3 is modulated by aqueous humor growth factors</title><title>Experimental eye research</title><addtitle>Exp Eye Res</addtitle><description>We investigated the mRNA and protein expression of fibronectin and stromelysin-1 (matrix metalloproteinase-3, MMP-3) by trabecular cells treated with growth factors present in primary and secondary aqueous humors. Serum-deprived trabecular cells were incubated for 48
hr or 7 days in medium containing either primary or secondary aqueous humor growth factors or in serum-free medium. We extracted total RNA, performed reverse transcription-polymerase chain reaction using primer pairs for fibronectin, stromelysin-1 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and quantified the products. We utilized Western blotting to detect and quantify fibronectin and stromelysin-1 protein. Compared to controls, expression of fibronectin mRNA by trabecular cells was increased by 50 and 100% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 50 and 130% after incubation in secondary aqueous humor growth factors. Stromelysin-1 mRNA expression was decreased by 25 and 50% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 80 and 85% after incubation for 48
hr or 7 days, respectively, in secondary aqueous humor growth factors. Fibronectin protein increased 3·5-fold and 6-fold after incubation for 48
hr with primary or secondary aqueous humor growth factors, respectively; after 7 days, the level increased 4- and 7-folds, respectively. Stromelysin-1 protein was not detectable by western blotting. The up-regulation of fibronectin mRNA by trabecular cells exposed to growth factors present in secondary aqueous humor augmented by the down-regulation of stromelysin-1 mRNA contributed to the accumulation of fibronectin. Our findings open the possibility that induction of stromelysin-1 gene expression in the trabecular meshwork of glaucomatous eyes could effectively reduce buildup of fibronectin in the aqueous outflow pathway to decrease outflow resistance in glaucomatous states of the eye.</description><subject>Animals</subject><subject>Aqueous Humor - chemistry</subject><subject>Cells, Cultured</subject><subject>Culture Media, Serum-Free</subject><subject>Fibronectins - genetics</subject><subject>Fibronectins - metabolism</subject><subject>Gene Expression Regulation - drug effects</subject><subject>gene therapy</subject><subject>glaucoma</subject><subject>Growth Substances - pharmacology</subject><subject>Matrix Metalloproteinase 3 - genetics</subject><subject>Matrix Metalloproteinase 3 - metabolism</subject><subject>primary aqueous humor</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>RNA, Messenger - genetics</subject><subject>secondary aqueous humor</subject><subject>Swine</subject><subject>trabecular meshwork</subject><subject>Trabecular Meshwork - drug effects</subject><subject>Trabecular Meshwork - metabolism</subject><subject>western blot</subject><issn>0014-4835</issn><issn>1096-0007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM1P3DAQxS1EVba0_wAH5BO3pOPYjhOJC0J8VAK1B3p2HXsCXm3ixU74-O_raFfixmk0o_ee5v0IOWFQMmD1z3WJbxjLCoCX0JbA2AFZMWjrAgDUIVkBMFGIhssj8i2ldb5yocRXcsQkg7oVckX-PUTToZ03JlKLmw3Ft23ElHwYaehp77sYRrSTH6kZHb2__1Nw6hMdgsueCR3t3ql5njHMiT7NQ4j0MYbX6Yn2xk4hpu_kS282CX_s5zH5e331cHlb3P2--XV5cVdYLqupqCuBgrcNILPKSqlkJxpVd53MC7bYCzSmahqW27LKOadkw5u25SCMsqbix-Rsl7uNIb-TJj34tDQy4_KbVqypK65UFlY7oY0hpYi93kY_mPiuGeiFq17rhateuGpodeaaTaf79Lkb0H1Y9iCz4HwnwNzxxWd7sh5Hi87HjE-74D_L_w96OolT</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Tripathi, Brenda J.</creator><creator>Tripathi, Ramesh C.</creator><creator>Chen, Jianguang</creator><creator>Gotsis, Stelios</creator><creator>Li, Junping</creator><general>Elsevier 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></search><sort><creationdate>20040301</creationdate><title>Trabecular cell expression of fibronectin and MMP-3 is modulated by aqueous humor growth factors</title><author>Tripathi, Brenda J. ; Tripathi, Ramesh C. ; Chen, Jianguang ; Gotsis, Stelios ; Li, Junping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c352t-624e43980e1c7c5575b4876bb5c55e9ef4eaa288120012ddd7583899304a7ca23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Aqueous Humor - chemistry</topic><topic>Cells, Cultured</topic><topic>Culture Media, Serum-Free</topic><topic>Fibronectins - genetics</topic><topic>Fibronectins - metabolism</topic><topic>Gene Expression Regulation - drug effects</topic><topic>gene therapy</topic><topic>glaucoma</topic><topic>Growth Substances - pharmacology</topic><topic>Matrix Metalloproteinase 3 - genetics</topic><topic>Matrix Metalloproteinase 3 - metabolism</topic><topic>primary aqueous humor</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><topic>RNA, Messenger - genetics</topic><topic>secondary aqueous humor</topic><topic>Swine</topic><topic>trabecular meshwork</topic><topic>Trabecular Meshwork - drug effects</topic><topic>Trabecular Meshwork - metabolism</topic><topic>western blot</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tripathi, Brenda J.</creatorcontrib><creatorcontrib>Tripathi, Ramesh C.</creatorcontrib><creatorcontrib>Chen, Jianguang</creatorcontrib><creatorcontrib>Gotsis, Stelios</creatorcontrib><creatorcontrib>Li, Junping</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><jtitle>Experimental eye research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tripathi, Brenda J.</au><au>Tripathi, Ramesh C.</au><au>Chen, Jianguang</au><au>Gotsis, Stelios</au><au>Li, Junping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trabecular cell expression of fibronectin and MMP-3 is modulated by aqueous humor growth factors</atitle><jtitle>Experimental eye research</jtitle><addtitle>Exp Eye Res</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>78</volume><issue>3</issue><spage>653</spage><epage>660</epage><pages>653-660</pages><issn>0014-4835</issn><eissn>1096-0007</eissn><abstract>We investigated the mRNA and protein expression of fibronectin and stromelysin-1 (matrix metalloproteinase-3, MMP-3) by trabecular cells treated with growth factors present in primary and secondary aqueous humors. Serum-deprived trabecular cells were incubated for 48
hr or 7 days in medium containing either primary or secondary aqueous humor growth factors or in serum-free medium. We extracted total RNA, performed reverse transcription-polymerase chain reaction using primer pairs for fibronectin, stromelysin-1 and glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and quantified the products. We utilized Western blotting to detect and quantify fibronectin and stromelysin-1 protein. Compared to controls, expression of fibronectin mRNA by trabecular cells was increased by 50 and 100% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 50 and 130% after incubation in secondary aqueous humor growth factors. Stromelysin-1 mRNA expression was decreased by 25 and 50% after incubation in primary aqueous humor growth factors for 48
hr or 7 days, respectively, and 80 and 85% after incubation for 48
hr or 7 days, respectively, in secondary aqueous humor growth factors. Fibronectin protein increased 3·5-fold and 6-fold after incubation for 48
hr with primary or secondary aqueous humor growth factors, respectively; after 7 days, the level increased 4- and 7-folds, respectively. Stromelysin-1 protein was not detectable by western blotting. The up-regulation of fibronectin mRNA by trabecular cells exposed to growth factors present in secondary aqueous humor augmented by the down-regulation of stromelysin-1 mRNA contributed to the accumulation of fibronectin. Our findings open the possibility that induction of stromelysin-1 gene expression in the trabecular meshwork of glaucomatous eyes could effectively reduce buildup of fibronectin in the aqueous outflow pathway to decrease outflow resistance in glaucomatous states of the eye.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>15106945</pmid><doi>10.1016/j.exer.2003.09.011</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Aqueous Humor - chemistry Cells, Cultured Culture Media, Serum-Free Fibronectins - genetics Fibronectins - metabolism Gene Expression Regulation - drug effects gene therapy glaucoma Growth Substances - pharmacology Matrix Metalloproteinase 3 - genetics Matrix Metalloproteinase 3 - metabolism primary aqueous humor Reverse Transcriptase Polymerase Chain Reaction RNA, Messenger - genetics secondary aqueous humor Swine trabecular meshwork Trabecular Meshwork - drug effects Trabecular Meshwork - metabolism western blot |
title | Trabecular cell expression of fibronectin and MMP-3 is modulated by aqueous humor growth factors |
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