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Anti-apoptotic effects of probucol are associated with downregulation of Daxx expression in THP-1 macrophage. | LitMetric

Anti-apoptotic effects of probucol are associated with downregulation of Daxx expression in THP-1 macrophage.

Cardiovasc Drugs Ther

Division of Pharmacoproteomics, Institute of Pharmacy & Pharmacology, Nanhua University, Changsheng Western Road 28#, Hengyang, 421001, Hunan, China.

Published: February 2007

AI Article Synopsis

  • - The study investigates how Daxx expression affects the antiapoptotic properties of probucol in THP-1 macrophages, particularly focusing on apoptosis induced by oxidized low-density lipoprotein (oxLDL).
  • - Results show that exposure to oxLDL significantly increases Daxx expression and promotes its movement into the cell nucleus, while probucol treatment before oxLDL exposure decreases Daxx levels and reduces apoptosis by over 61%.
  • - The findings conclude that the apoptosis in THP-1 macrophages caused by oxLDL is linked to increased Daxx, and that probucol's protective effect involves reducing Daxx expression and preventing its translocation to the nucleus.

Article Abstract

Aim: To study the relationship between Daxx expression and the antiapoptotic effects of probucol in THP-1 macrophage.

Materials And Methods: Apoptosis of THP-1 derived macrophages was induced by exposure to oxidized low density lipoprotein (oxLDL). The development of apoptosis was determined by flow cytometry analysis and nucleic acid-binding dye acridin orange. Reverse transcriptase-polymerase chain reaction (RT-PCR), Western blotting and indirect immunofluorescence were used to evaluate the expression of Daxx and caspase-3 at both mRNA and protein level.

Results: As expected, THP-1 macrophages exposed to 100 mg/l oxLDL for 48 h exhibited typical morphologic changes of apoptosis, including condensed chromatin and shrunken nucleus. oxLDL treatment markedly increased Daxx expression in a time- and dose-dependent manner, and facilitated Daxx translocation from cytoplasm to nucleus. The percentage of cells with Daxx in nuclei was significantly increased from 8 to 59%. Treatment with probucol (50 micromol/l) for 4 h prior to exposure to oxLDL significantly inhibited Daxx expression and THP-1 macrophage apoptosis by 61.3%. Furthermore, oxLDL enhanced caspase-3 expression with increased mRNA and protein levels, but without obvious change in translocation of caspase-3 (the cells with nuclear Daxx: 14 vs 8%). In contrast, probucol attenuated oxLDL-stimulated caspase-3 expression in THP-1 macrophages.

Conclusion: OxLDL-induced apoptosis of THP-1 macrophage is associated with Daxx up-regulation; while inhibition of apoptosis by probucol is related to decreased Daxx expression and nuclear translocation.

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Source
http://dx.doi.org/10.1007/s10557-007-6002-xDOI Listing

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