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Evidence of a direct role for Bcl-2 in the regulation of articular chondrocyte apoptosis under the conditions of serum withdrawal and retinoic acid treatment
The regulation of chondrocyte apoptosis in articular cartilage may underlay age‐associated changes in cartilage and the development of osteoarthritis. Here we demonstrate the importance of Bcl‐2 in regulating articular chondrocyte apoptosis in response to both serum withdrawal and retinoic acid trea...
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Published in: | Journal of cellular biochemistry 1998-11, Vol.71 (2), p.302-309 |
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creator | Feng, Lixin Precht, Patricia Balakir, Richard Horton Jr, Walter E. |
description | The regulation of chondrocyte apoptosis in articular cartilage may underlay age‐associated changes in cartilage and the development of osteoarthritis. Here we demonstrate the importance of Bcl‐2 in regulating articular chondrocyte apoptosis in response to both serum withdrawal and retinoic acid treatment. Both stimuli induced apoptosis of primary human articular chondrocytes and a rat chondrocyte cell line as evidenced by the formation of DNA ladders. Apoptosis was accompanied by decreased expression of aggrecan, a chondrocyte specific matrix protein. The expression of Bcl‐2 was downregulated by both agents based on Northern and Western analysis, while the level of Bax expression remained unchanged compared to control cells. The importance of Bcl‐2 in regulating chondrocyte apoptosis was confirmed by creating cell lines overexpressing sense and antisense Bcl‐2 mRNA. Multiple cell lines expressing antisense Bcl‐2 displayed increased apoptosis even in the presence of 10% serum as compared to wild‐type cells. In contrast, chondrocytes overexpressing Bcl‐2 were resistant to apoptosis induced by both serum withdrawal and retinoic acid treatment. Finally, the expression of Bcl‐2 did not block the decreased aggrecan expression in IRC cells treated with retinoic acid. We conclude that Bcl‐2 plays an important role in the maintenance of articular chondrocyte survival and that retinoic acid inhibits aggrecan expression independent of the apoptotic process. J. Cell. Biochem. 71:302–309, 1998. © 1998 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/(SICI)1097-4644(19981101)71:2<302::AID-JCB14>3.0.CO;2-M |
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Here we demonstrate the importance of Bcl‐2 in regulating articular chondrocyte apoptosis in response to both serum withdrawal and retinoic acid treatment. Both stimuli induced apoptosis of primary human articular chondrocytes and a rat chondrocyte cell line as evidenced by the formation of DNA ladders. Apoptosis was accompanied by decreased expression of aggrecan, a chondrocyte specific matrix protein. The expression of Bcl‐2 was downregulated by both agents based on Northern and Western analysis, while the level of Bax expression remained unchanged compared to control cells. The importance of Bcl‐2 in regulating chondrocyte apoptosis was confirmed by creating cell lines overexpressing sense and antisense Bcl‐2 mRNA. Multiple cell lines expressing antisense Bcl‐2 displayed increased apoptosis even in the presence of 10% serum as compared to wild‐type cells. In contrast, chondrocytes overexpressing Bcl‐2 were resistant to apoptosis induced by both serum withdrawal and retinoic acid treatment. Finally, the expression of Bcl‐2 did not block the decreased aggrecan expression in IRC cells treated with retinoic acid. We conclude that Bcl‐2 plays an important role in the maintenance of articular chondrocyte survival and that retinoic acid inhibits aggrecan expression independent of the apoptotic process. J. Cell. Biochem. 71:302–309, 1998. © 1998 Wiley‐Liss, Inc.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/(SICI)1097-4644(19981101)71:2<302::AID-JCB14>3.0.CO;2-M</identifier><identifier>PMID: 9779827</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Aged ; aging ; Animals ; Apoptosis - drug effects ; Blood ; cartilage ; Cartilage, Articular - cytology ; Cartilage, Articular - drug effects ; Cartilage, Articular - metabolism ; cell culture ; Cells, Cultured ; Gene Expression - drug effects ; human ; Humans ; osteoarthritis ; programmed cell death ; Proto-Oncogene Proteins c-bcl-2 - physiology ; Rabbits ; Rats ; Tretinoin - pharmacology</subject><ispartof>Journal of cellular biochemistry, 1998-11, Vol.71 (2), p.302-309</ispartof><rights>Copyright © 1998 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3204-b1bc1771273027a82eb87bab27312f2fcbf21b8710319e01ed604d8139b7c3463</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9779827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feng, Lixin</creatorcontrib><creatorcontrib>Precht, Patricia</creatorcontrib><creatorcontrib>Balakir, Richard</creatorcontrib><creatorcontrib>Horton Jr, Walter E.</creatorcontrib><title>Evidence of a direct role for Bcl-2 in the regulation of articular chondrocyte apoptosis under the conditions of serum withdrawal and retinoic acid treatment</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>The regulation of chondrocyte apoptosis in articular cartilage may underlay age‐associated changes in cartilage and the development of osteoarthritis. Here we demonstrate the importance of Bcl‐2 in regulating articular chondrocyte apoptosis in response to both serum withdrawal and retinoic acid treatment. Both stimuli induced apoptosis of primary human articular chondrocytes and a rat chondrocyte cell line as evidenced by the formation of DNA ladders. Apoptosis was accompanied by decreased expression of aggrecan, a chondrocyte specific matrix protein. The expression of Bcl‐2 was downregulated by both agents based on Northern and Western analysis, while the level of Bax expression remained unchanged compared to control cells. The importance of Bcl‐2 in regulating chondrocyte apoptosis was confirmed by creating cell lines overexpressing sense and antisense Bcl‐2 mRNA. Multiple cell lines expressing antisense Bcl‐2 displayed increased apoptosis even in the presence of 10% serum as compared to wild‐type cells. In contrast, chondrocytes overexpressing Bcl‐2 were resistant to apoptosis induced by both serum withdrawal and retinoic acid treatment. Finally, the expression of Bcl‐2 did not block the decreased aggrecan expression in IRC cells treated with retinoic acid. We conclude that Bcl‐2 plays an important role in the maintenance of articular chondrocyte survival and that retinoic acid inhibits aggrecan expression independent of the apoptotic process. J. Cell. Biochem. 71:302–309, 1998. © 1998 Wiley‐Liss, Inc.</description><subject>Aged</subject><subject>aging</subject><subject>Animals</subject><subject>Apoptosis - drug effects</subject><subject>Blood</subject><subject>cartilage</subject><subject>Cartilage, Articular - cytology</subject><subject>Cartilage, Articular - drug effects</subject><subject>Cartilage, Articular - metabolism</subject><subject>cell culture</subject><subject>Cells, Cultured</subject><subject>Gene Expression - drug effects</subject><subject>human</subject><subject>Humans</subject><subject>osteoarthritis</subject><subject>programmed cell death</subject><subject>Proto-Oncogene Proteins c-bcl-2 - physiology</subject><subject>Rabbits</subject><subject>Rats</subject><subject>Tretinoin - pharmacology</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><recordid>eNqFkV1v0zAUhiMEGmXwE5B8hbaLFH-EOCkItIZtFLZW4mvcWY5zshrSuNgOpT-G_4rTlN6AxJXlc97zHFtPFL0ieEwwpk9PPsyK2SnBOY-TNElOSJ5nhGByysmEvmCYTiZns9fx22JKkpdsjMfF4jmNr-9Eo8PM3WiEOcMxZYTejx449xVjnOeMHkVHOed5Rvko-nX-Q1fQKkCmRhJV2oLyyJoGUG0smqompki3yC8BWbjtGum1aXdh67UKd4vU0rSVNWrrAcm1WXvjtENdW4HdzanQ1v2Y6-cc2G6FNtovKys3skGyrQLa69ZohaTSFfIWpF9B6x9G92rZOHi0P4-jTxfnH4s38dXiclacXcWKUZzEJSkV4ZzQ8F3KZUahzHgpy3AntKa1KmtKQolgRnLABKoUJ1VGWF5yxZKUHUdPBu7amu8dOC9W2iloGtmC6ZxI8zygUhKCN0NQWeOchVqsrV5JuxUEi16cEL040UsQvQTxR5zgRFDB-kQQJ3biBBNYFItQvw7kx_sndOUKqgN3byr0vwz9jW5g-9fa_27919KhENDxgNbOw88DWtpvIuWMPxM380vxfv7uYp58zsSU_QYNYcTk</recordid><startdate>19981101</startdate><enddate>19981101</enddate><creator>Feng, Lixin</creator><creator>Precht, Patricia</creator><creator>Balakir, Richard</creator><creator>Horton Jr, Walter E.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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></search><sort><creationdate>19981101</creationdate><title>Evidence of a direct role for Bcl-2 in the regulation of articular chondrocyte apoptosis under the conditions of serum withdrawal and retinoic acid treatment</title><author>Feng, Lixin ; Precht, Patricia ; Balakir, Richard ; Horton Jr, Walter E.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3204-b1bc1771273027a82eb87bab27312f2fcbf21b8710319e01ed604d8139b7c3463</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Aged</topic><topic>aging</topic><topic>Animals</topic><topic>Apoptosis - drug effects</topic><topic>Blood</topic><topic>cartilage</topic><topic>Cartilage, Articular - cytology</topic><topic>Cartilage, Articular - drug effects</topic><topic>Cartilage, Articular - metabolism</topic><topic>cell culture</topic><topic>Cells, Cultured</topic><topic>Gene Expression - drug effects</topic><topic>human</topic><topic>Humans</topic><topic>osteoarthritis</topic><topic>programmed cell death</topic><topic>Proto-Oncogene Proteins c-bcl-2 - physiology</topic><topic>Rabbits</topic><topic>Rats</topic><topic>Tretinoin - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feng, Lixin</creatorcontrib><creatorcontrib>Precht, Patricia</creatorcontrib><creatorcontrib>Balakir, Richard</creatorcontrib><creatorcontrib>Horton Jr, Walter E.</creatorcontrib><collection>Istex</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><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feng, Lixin</au><au>Precht, Patricia</au><au>Balakir, Richard</au><au>Horton Jr, Walter E.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evidence of a direct role for Bcl-2 in the regulation of articular chondrocyte apoptosis under the conditions of serum withdrawal and retinoic acid treatment</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>1998-11-01</date><risdate>1998</risdate><volume>71</volume><issue>2</issue><spage>302</spage><epage>309</epage><pages>302-309</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>The regulation of chondrocyte apoptosis in articular cartilage may underlay age‐associated changes in cartilage and the development of osteoarthritis. Here we demonstrate the importance of Bcl‐2 in regulating articular chondrocyte apoptosis in response to both serum withdrawal and retinoic acid treatment. Both stimuli induced apoptosis of primary human articular chondrocytes and a rat chondrocyte cell line as evidenced by the formation of DNA ladders. Apoptosis was accompanied by decreased expression of aggrecan, a chondrocyte specific matrix protein. The expression of Bcl‐2 was downregulated by both agents based on Northern and Western analysis, while the level of Bax expression remained unchanged compared to control cells. The importance of Bcl‐2 in regulating chondrocyte apoptosis was confirmed by creating cell lines overexpressing sense and antisense Bcl‐2 mRNA. Multiple cell lines expressing antisense Bcl‐2 displayed increased apoptosis even in the presence of 10% serum as compared to wild‐type cells. In contrast, chondrocytes overexpressing Bcl‐2 were resistant to apoptosis induced by both serum withdrawal and retinoic acid treatment. Finally, the expression of Bcl‐2 did not block the decreased aggrecan expression in IRC cells treated with retinoic acid. We conclude that Bcl‐2 plays an important role in the maintenance of articular chondrocyte survival and that retinoic acid inhibits aggrecan expression independent of the apoptotic process. J. Cell. 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subjects | Aged aging Animals Apoptosis - drug effects Blood cartilage Cartilage, Articular - cytology Cartilage, Articular - drug effects Cartilage, Articular - metabolism cell culture Cells, Cultured Gene Expression - drug effects human Humans osteoarthritis programmed cell death Proto-Oncogene Proteins c-bcl-2 - physiology Rabbits Rats Tretinoin - pharmacology |
title | Evidence of a direct role for Bcl-2 in the regulation of articular chondrocyte apoptosis under the conditions of serum withdrawal and retinoic acid treatment |
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