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Inhibition of D1, D2, and a cyclin expression in HL-60 cells by the lipid peroxydation product 4-hydroxynonenal
被引:47
|作者:
Pizzimenti, S
Barrera, G
Dianzani, MU
Brüsselbach, S
机构:
[1] Univ Turin, Dipartimento Med & Oncol Sperimentale, Sez Patol Gen, I-10125 Turin, Italy
[2] Univ Marburg, IMT, Marburg, Germany
关键词:
lipid peroxidation;
4-hydroxynonenal;
HL-60 cell line;
proliferation;
cyclins;
CDKs;
free radicals;
D O I:
10.1016/S0891-5849(99)00022-2
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
4-Hydroxynonenal (HNE), a product of lipid peroxidation. is an highly reactive aldehyde that, at concentration similar to those found in normal cells, blocks proliferation and induces a granulocytic-like differentiation in HL-60 cells. These effects are accompained by a marked increase in the proportion G0/G1 cells. The mechanisms of HNE action were investigated by analyzing the expression of the cyclins and cyclin-dependent protein kinases (CDKs), controlling the cell cycle progression. Data obtained by exposing cells to dimethyl sulfoxide (DMSO) were used for comparison. 4-Hydroxynonenal downregulated both mRNA and protein contents of cyclins D1, D2, and A until 24 h from the treatments, whereas DMSO inhibited cyclin D1 and D2 expression until the end of experiment (2 days) and induces an increase of cyclin A until 1 day. Cyclins B and E, and protein kinase CDK2 and CDK4 expressions were not affected by HNE, whereas DMSO induced an increase of cyclin E, B, and CDK2 from 8 h to 1 day. These data are in agreement with previous results indicating a different time-course of accumulation in G0/G1 phases of cells treated with HNE and DMSO and suggest that the HNE inhibitory effect on proliferation and cell cycle progression may depend by the downregulation of D1, D2, and A cyclin expression. (C) 1999 Elsevier Science Inc.
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页码:1578 / 1586
页数:9
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