Myocilin Regulates Cell Proliferation and Survival
Myocilin, a causative gene for open angle glaucoma, encodes a secreted glycoprotein with poorly understood functions. To gain insight into its functions, we produced a stably transfected HEK293 cell line expressing myocilin under an inducible promoter and compared gene expression profiles between my...
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Veröffentlicht in: | The Journal of biological chemistry 2014-04, Vol.289 (14), p.10155-10167 |
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description | Myocilin, a causative gene for open angle glaucoma, encodes a secreted glycoprotein with poorly understood functions. To gain insight into its functions, we produced a stably transfected HEK293 cell line expressing myocilin under an inducible promoter and compared gene expression profiles between myocilin-expressing and vector control cell lines by a microarray analysis. A significant fraction of differentially expressed genes in myocilin-expressing cells was associated with cell growth and cell death, suggesting that myocilin may have a role in the regulation of cell growth and survival. Increased proliferation of myocilin-expressing cells was demonstrated by the WST-1 proliferation assay, direct cell counting, and immunostaining with antibodies against Ki-67, a cellular proliferation marker. Myocilin-containing conditioned medium also increased proliferation of unmodified HEK293 cells. Myocilin-expressing cells were more resistant to serum starvation-induced apoptosis than control cells. TUNEL-positive apoptotic cells were dramatically decreased, and two apoptotic marker proteins, cleaved caspase 7 and cleaved poly(ADP-ribose) polymerase, were significantly reduced in myocilin-expressing cells as compared with control cells under apoptotic conditions. In addition, myocilin-deficient mesenchymal stem cells exhibited reduced proliferation and enhanced susceptibility to serum starvation-induced apoptosis as compared with wild-type mesenchymal stem cells. Phosphorylation of ERK1/2 and its upstream kinases, c-Raf and MEK, was increased in myocilin-expressing cells compared with control cells. Elevated phosphorylation of ERK1/2 was also observed in the trabecular meshwork of transgenic mice expressing 6-fold higher levels of myocilin when compared with their wild-type littermates. These results suggest that myocilin promotes cell proliferation and resistance to apoptosis via the ERK1/2 MAPK signaling pathway.
Background: The physiological function(s) of myocilin, a glaucoma-associated protein, is poorly understood.
Results: Myocilin enhances cell proliferation and survival together with the activation of the ERK signaling pathway. Myocilin-deficient mesenchymal stem cells demonstrate reduced proliferation and survival.
Conclusion: Myocilin participates in the regulation of cell growth and survival.
Significance: This study provides new insight into the role of myocilin in ocular and non-ocular tissues. |
doi_str_mv | 10.1074/jbc.M113.547091 |
format | Article |
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Background: The physiological function(s) of myocilin, a glaucoma-associated protein, is poorly understood.
Results: Myocilin enhances cell proliferation and survival together with the activation of the ERK signaling pathway. Myocilin-deficient mesenchymal stem cells demonstrate reduced proliferation and survival.
Conclusion: Myocilin participates in the regulation of cell growth and survival.
Significance: This study provides new insight into the role of myocilin in ocular and non-ocular tissues.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M113.547091</identifier><identifier>PMID: 24563482</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Animals ; Apoptosis ; Apoptosis - physiology ; Caspase 7 - genetics ; Caspase 7 - metabolism ; Cell Biology ; Cell Growth ; Cell Proliferation ; Cell Signaling ; Cell Survival - physiology ; Cytoskeletal Proteins - genetics ; Cytoskeletal Proteins - metabolism ; ERK ; Eye Proteins - genetics ; Eye Proteins - metabolism ; Glycoproteins - genetics ; Glycoproteins - metabolism ; HEK293 Cells ; Humans ; MAP Kinase Signaling System - physiology ; Mesenchymal Stem Cells ; Mesenchymal Stem Cells - cytology ; Mesenchymal Stem Cells - metabolism ; Mice ; Mice, Transgenic ; Mitogen-Activated Protein Kinase 1 - genetics ; Mitogen-Activated Protein Kinase 1 - metabolism ; Mitogen-Activated Protein Kinase 3 - genetics ; Mitogen-Activated Protein Kinase 3 - metabolism ; Phosphorylation - physiology</subject><ispartof>The Journal of biological chemistry, 2014-04, Vol.289 (14), p.10155-10167</ispartof><rights>2014 © 2014 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2014 by The American Society for Biochemistry and Molecular Biology, Inc. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c443t-c8ab5e902177207e1f82e16ca9e9ca6e21c3be1420318f72e79e34da63cdf5743</citedby><cites>FETCH-LOGICAL-c443t-c8ab5e902177207e1f82e16ca9e9ca6e21c3be1420318f72e79e34da63cdf5743</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/PMC3974985/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3974985/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24563482$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joe, Myung Kuk</creatorcontrib><creatorcontrib>Kwon, Heung Sun</creatorcontrib><creatorcontrib>Cojocaru, Radu</creatorcontrib><creatorcontrib>Tomarev, Stanislav I.</creatorcontrib><title>Myocilin Regulates Cell Proliferation and Survival</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Myocilin, a causative gene for open angle glaucoma, encodes a secreted glycoprotein with poorly understood functions. To gain insight into its functions, we produced a stably transfected HEK293 cell line expressing myocilin under an inducible promoter and compared gene expression profiles between myocilin-expressing and vector control cell lines by a microarray analysis. A significant fraction of differentially expressed genes in myocilin-expressing cells was associated with cell growth and cell death, suggesting that myocilin may have a role in the regulation of cell growth and survival. Increased proliferation of myocilin-expressing cells was demonstrated by the WST-1 proliferation assay, direct cell counting, and immunostaining with antibodies against Ki-67, a cellular proliferation marker. Myocilin-containing conditioned medium also increased proliferation of unmodified HEK293 cells. Myocilin-expressing cells were more resistant to serum starvation-induced apoptosis than control cells. TUNEL-positive apoptotic cells were dramatically decreased, and two apoptotic marker proteins, cleaved caspase 7 and cleaved poly(ADP-ribose) polymerase, were significantly reduced in myocilin-expressing cells as compared with control cells under apoptotic conditions. In addition, myocilin-deficient mesenchymal stem cells exhibited reduced proliferation and enhanced susceptibility to serum starvation-induced apoptosis as compared with wild-type mesenchymal stem cells. Phosphorylation of ERK1/2 and its upstream kinases, c-Raf and MEK, was increased in myocilin-expressing cells compared with control cells. Elevated phosphorylation of ERK1/2 was also observed in the trabecular meshwork of transgenic mice expressing 6-fold higher levels of myocilin when compared with their wild-type littermates. These results suggest that myocilin promotes cell proliferation and resistance to apoptosis via the ERK1/2 MAPK signaling pathway.
Background: The physiological function(s) of myocilin, a glaucoma-associated protein, is poorly understood.
Results: Myocilin enhances cell proliferation and survival together with the activation of the ERK signaling pathway. Myocilin-deficient mesenchymal stem cells demonstrate reduced proliferation and survival.
Conclusion: Myocilin participates in the regulation of cell growth and survival.
Significance: This study provides new insight into the role of myocilin in ocular and non-ocular tissues.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Apoptosis - physiology</subject><subject>Caspase 7 - genetics</subject><subject>Caspase 7 - metabolism</subject><subject>Cell Biology</subject><subject>Cell Growth</subject><subject>Cell Proliferation</subject><subject>Cell Signaling</subject><subject>Cell Survival - physiology</subject><subject>Cytoskeletal Proteins - genetics</subject><subject>Cytoskeletal Proteins - metabolism</subject><subject>ERK</subject><subject>Eye Proteins - genetics</subject><subject>Eye Proteins - metabolism</subject><subject>Glycoproteins - genetics</subject><subject>Glycoproteins - metabolism</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>MAP Kinase Signaling System - physiology</subject><subject>Mesenchymal Stem Cells</subject><subject>Mesenchymal Stem Cells - cytology</subject><subject>Mesenchymal Stem Cells - metabolism</subject><subject>Mice</subject><subject>Mice, Transgenic</subject><subject>Mitogen-Activated Protein Kinase 1 - genetics</subject><subject>Mitogen-Activated Protein Kinase 1 - metabolism</subject><subject>Mitogen-Activated Protein Kinase 3 - genetics</subject><subject>Mitogen-Activated Protein Kinase 3 - metabolism</subject><subject>Phosphorylation - physiology</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kDtLBDEURoMouj5qO5nSZtbcPDaTRpDFFyiKD7AL2cwdjcxONJlZ8N-bZVW08DYp7smXL4eQfaBjoEocvc7c-BqAj6VQVMMaGQGteMklPK2TEaUMSs1ktUW2U3qleYSGTbLFhJxwUbERYdcfwfnWd8UdPg-t7TEVU2zb4jaG1jcYbe9DV9iuLu6HuPAL2-6Sjca2Cfe-zh3yeHb6ML0or27OL6cnV6UTgvelq-xMos4VlGJUITQVQ5g4q1E7O0EGjs8QBKMcqkYxVBq5qO2Eu7qRSvAdcrzKfRtmc6wddn20rXmLfm7jhwnWm7-bzr-Y57AwXCuhK5kDDr8CYngfMPVm7pPLn7MdhiEZkCAE01LrjB6tUBdDShGbn2eAmqVpk02bpWmzMp1vHPxu98N_q82AXgGYHS08RpOcx85h7SO63tTB_xv-CQwFjZA</recordid><startdate>20140404</startdate><enddate>20140404</enddate><creator>Joe, Myung Kuk</creator><creator>Kwon, Heung Sun</creator><creator>Cojocaru, Radu</creator><creator>Tomarev, Stanislav I.</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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><scope>5PM</scope></search><sort><creationdate>20140404</creationdate><title>Myocilin Regulates Cell Proliferation and Survival</title><author>Joe, Myung Kuk ; Kwon, Heung Sun ; Cojocaru, Radu ; Tomarev, Stanislav I.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c443t-c8ab5e902177207e1f82e16ca9e9ca6e21c3be1420318f72e79e34da63cdf5743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Apoptosis - physiology</topic><topic>Caspase 7 - genetics</topic><topic>Caspase 7 - metabolism</topic><topic>Cell Biology</topic><topic>Cell Growth</topic><topic>Cell Proliferation</topic><topic>Cell Signaling</topic><topic>Cell Survival - physiology</topic><topic>Cytoskeletal Proteins - genetics</topic><topic>Cytoskeletal Proteins - metabolism</topic><topic>ERK</topic><topic>Eye Proteins - genetics</topic><topic>Eye Proteins - metabolism</topic><topic>Glycoproteins - genetics</topic><topic>Glycoproteins - metabolism</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>MAP Kinase Signaling System - physiology</topic><topic>Mesenchymal Stem Cells</topic><topic>Mesenchymal Stem Cells - cytology</topic><topic>Mesenchymal Stem Cells - metabolism</topic><topic>Mice</topic><topic>Mice, Transgenic</topic><topic>Mitogen-Activated Protein Kinase 1 - genetics</topic><topic>Mitogen-Activated Protein Kinase 1 - metabolism</topic><topic>Mitogen-Activated Protein Kinase 3 - genetics</topic><topic>Mitogen-Activated Protein Kinase 3 - metabolism</topic><topic>Phosphorylation - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joe, Myung Kuk</creatorcontrib><creatorcontrib>Kwon, Heung Sun</creatorcontrib><creatorcontrib>Cojocaru, Radu</creatorcontrib><creatorcontrib>Tomarev, Stanislav I.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joe, Myung Kuk</au><au>Kwon, Heung Sun</au><au>Cojocaru, Radu</au><au>Tomarev, Stanislav I.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Myocilin Regulates Cell Proliferation and Survival</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2014-04-04</date><risdate>2014</risdate><volume>289</volume><issue>14</issue><spage>10155</spage><epage>10167</epage><pages>10155-10167</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Myocilin, a causative gene for open angle glaucoma, encodes a secreted glycoprotein with poorly understood functions. To gain insight into its functions, we produced a stably transfected HEK293 cell line expressing myocilin under an inducible promoter and compared gene expression profiles between myocilin-expressing and vector control cell lines by a microarray analysis. A significant fraction of differentially expressed genes in myocilin-expressing cells was associated with cell growth and cell death, suggesting that myocilin may have a role in the regulation of cell growth and survival. Increased proliferation of myocilin-expressing cells was demonstrated by the WST-1 proliferation assay, direct cell counting, and immunostaining with antibodies against Ki-67, a cellular proliferation marker. Myocilin-containing conditioned medium also increased proliferation of unmodified HEK293 cells. Myocilin-expressing cells were more resistant to serum starvation-induced apoptosis than control cells. TUNEL-positive apoptotic cells were dramatically decreased, and two apoptotic marker proteins, cleaved caspase 7 and cleaved poly(ADP-ribose) polymerase, were significantly reduced in myocilin-expressing cells as compared with control cells under apoptotic conditions. In addition, myocilin-deficient mesenchymal stem cells exhibited reduced proliferation and enhanced susceptibility to serum starvation-induced apoptosis as compared with wild-type mesenchymal stem cells. Phosphorylation of ERK1/2 and its upstream kinases, c-Raf and MEK, was increased in myocilin-expressing cells compared with control cells. Elevated phosphorylation of ERK1/2 was also observed in the trabecular meshwork of transgenic mice expressing 6-fold higher levels of myocilin when compared with their wild-type littermates. These results suggest that myocilin promotes cell proliferation and resistance to apoptosis via the ERK1/2 MAPK signaling pathway.
Background: The physiological function(s) of myocilin, a glaucoma-associated protein, is poorly understood.
Results: Myocilin enhances cell proliferation and survival together with the activation of the ERK signaling pathway. Myocilin-deficient mesenchymal stem cells demonstrate reduced proliferation and survival.
Conclusion: Myocilin participates in the regulation of cell growth and survival.
Significance: This study provides new insight into the role of myocilin in ocular and non-ocular tissues.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24563482</pmid><doi>10.1074/jbc.M113.547091</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Apoptosis Apoptosis - physiology Caspase 7 - genetics Caspase 7 - metabolism Cell Biology Cell Growth Cell Proliferation Cell Signaling Cell Survival - physiology Cytoskeletal Proteins - genetics Cytoskeletal Proteins - metabolism ERK Eye Proteins - genetics Eye Proteins - metabolism Glycoproteins - genetics Glycoproteins - metabolism HEK293 Cells Humans MAP Kinase Signaling System - physiology Mesenchymal Stem Cells Mesenchymal Stem Cells - cytology Mesenchymal Stem Cells - metabolism Mice Mice, Transgenic Mitogen-Activated Protein Kinase 1 - genetics Mitogen-Activated Protein Kinase 1 - metabolism Mitogen-Activated Protein Kinase 3 - genetics Mitogen-Activated Protein Kinase 3 - metabolism Phosphorylation - physiology |
title | Myocilin Regulates Cell Proliferation and Survival |
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