Heat shock protein 60 modified with O-linked N-acetylglucosamine is involved in pancreatic beta-cell death under hyperglycemic conditions |
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Authors: | Kim Hoe Suk Kim Eun Mi Lee Jiae Yang Won Ho Park Tae Yoon Kim Young Min Cho Jin Won |
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Affiliation: | Department of Biology, Yonsei University, 134 Shinchon-dong, Seodaemun-gu, Seoul 120-749, Republic of Korea. |
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Abstract: | The objective of this study was to identify proteins modified with O-linked N-acetylglucosamine (O-GlcNAc) in pancreatic beta-cells and to understand their roles in cell death under hyperglycemic conditions. Here we report that heat shock protein 60 (HSP60) is modified with O-GlcNAc. Levels of O-GlcNAcylated HSP60 increased twofold in response to hyperglycemic conditions. HSP60 is a chaperonin known to bind to Bax in the cytoplasm under normoglycemic conditions. Under hyperglycemic conditions, Bax detached from O-GlcNAcylated HSP60 and translocated to mitochondria. Hyperglycemic conditions were also associated with cytochrome c release, caspase-3 activation, and cell death, suggesting that elevated O-GlcNAcylation of HSP60 interferes with HSP60-Bax interactions, leading to pancreatic beta-cell death. |
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Keywords: | HSP, heat shock protein O-GlcNAc, O-linked N-acetylglucosamine OGT, O-GlcNAc transferase O-GlcNAcase, N-acetylglucosaminidase HG, hyperglycemia NG, normoglycemia Mito, mitochondrial fraction Cyto, cytosolic fraction Cyto c, cytochrome c |
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