OxLDL and macrophage survival: essential and oxygen-independent involvement of the Hif-pathway
- نوع فایل : کتاب
- زبان : انگلیسی
- مؤلف : David M. Poitz Antje Augstein So¨nke Weinert Ru¨diger C. Braun-Dullaeus Ruth H. Strasser Alexander Schmeisser
- چاپ و سال / کشور: 2011
Description
Atherosclerotic plaques are characterized by hypoxic even anoxic areas and by high concentrations of oxidized lipoproteins. Moreover, unstable plaques attract a high number of macrophages despite the proapoptotic background within these plaques. Recently, it was shown that these macrophages are positive for Hif-1a. This subunit is a part of hypoxia-inducible factor 1 (Hif-1), a key transcriptional factor under hypoxia. Till date, it is not understood whether the Hif-system (consisting of Hif-1, Hif-2 and Hif-3) is involved in protection of macrophages under these proatherogenic conditions. The present study delineates that oxLDL causes fundamental changes in the regulation of the Hif-system in primary human macrophages. First, both oxLDL and hypoxia mediate accumulation of Hif-1a protein. Second, treatment with a combination of oxLDL and hypoxia is acting in an additive manner on Hif-1a protein content. Third, oxLDL alone does not increase Hif-2a protein, but abolishes the hypoxic induction of Hif-2a completely. OxLDL treatment alone was not toxic for macrophages under neither normoxia nor hypoxia. But, inhibition of Hif-pathway by adenoviral expression of a dominant-negative mutant combined with oxLDL treatment independently of the oxygen tension leads to apoptosis, as determined by caspase-3 activation and induction of DNA fragmentation. Furthermore, this inhibition also mediates the opening of the mitochondrial permeability transition pore. In conclusion, the present data show that Hif-1a regulation is essential for survival of oxLDL-treated macrophages independent of the oxygen tension. Therefore, this newly characterized mechanism might also have an important influence for the vulnerability of atherosclerotic plaques
Basic Res Cardiol (2011) 106:761–772
