NF-kappa B inhibition compromises cardiac fibroblast viability under hypoxia

dc.contributorSangeetha, M.
dc.contributorPillai, Malini S.
dc.contributorPhilip, Linda
dc.contributorLakatta, Edward G.
dc.contributorShivakumar, K.
dc.date.accessioned2012-12-04T11:44:43Z
dc.date.available2012-12-04T11:44:43Z
dc.date.issued2011
dc.description.abstractCardiac fibroblasts are reported to be relatively resistant to stress stimuli compared to cardiac myocytes and fibroblasts of non-cardiac origin. However, the mechanisms that facilitate their survival under conditions of stress remain unclear. We explored the possibility that NF-kappa B protects cardiac fibroblasts from hypoxia-induced cell death. Further, we examined the expression of the antiapoptotic clAP-2 and Bcl-2 in hypoxic cardiac fibroblasts, and their possible regulation by NF-kappa B. Phase contrast microscopy and propidium iodide staining revealed that cardiac fibroblasts are more resistant than pulmonary fibroblasts to hypoxia. Electrophoretic Mobility Shift Assay showed that hypoxia activates NF-kappa B in cardiac fibroblasts. Supershift assay indicated that the active NF-kappa B complex is a p65/p50 heterodimer. An I-kappa B-super-repressor was constructed that prevented NF-kappa B activation and compromised cell viability under hypoxic but not normoxic conditions. Similar results were obtained with Bay 11-7085, an inhibitor of NF-kappa B. Western blot analysis showed constitutive levels of Bcl-2 and hypoxic induction of clAP-2 in these cells. NF-kappa B inhibition reduced clAP-2 but not Bcl-2 levels in hypoxic cardiac fibroblasts. The results show for the first time that NF-kappa B is an important effector of survival in cardiac fibroblasts under hypoxic stress and that regulation of clAP-2 expression may contribute to its pro-survival role. (C) 2011 Elsevier Inc. All rights reserved.
dc.identifier.citationEXPERIMENTAL CELL RESEARCH. 317; 7; 899-909en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.yexcr.2010.12.024
dc.identifier.urihttps://dspace.sctimst.ac.in/handle/123456789/794
dc.publisherEXPERIMENTAL CELL RESEARCH
dc.subjectCardiology
dc.titleNF-kappa B inhibition compromises cardiac fibroblast viability under hypoxia
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