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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
Main Authors: Feng, Lixin, Precht, Patricia, Balakir, Richard, Horton Jr, Walter E.
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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. 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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. 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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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