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Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms.

Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Research Abstract Details 

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  • Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Abstract Text:

    wei zhangWei Zhang,yaping zhangYaping Zhang,lars edvinssonLars Edvinsson,cang-bao xuCang-Bao Xu,wei zhangWei Zhang,yaping zhangYaping Zhang,lars edvinssonLars Edvinsson,cang-bao xuCang-Bao Xu,

    Atherosclerosis is a key factor in vascular disease, and cigarette smoking is a well-known risk factor that may induce an inflammatory response and enhance plaque formation in arteries. Thromboxane (Tx) is one key inflammatory mediator involved in the pathogenesis of cardiovascular disease. The present study was designed to test if lipid soluble smoking particles (DSP) enhance TxA(2) receptor (TP) expression in rat mesenteric arteries, and if intracellular mitogen-activated protein kinase (MAPK) pathways play a role. Organ culture of rat mesenteric arteries in the presence of DSP (0.2 microl/ml for 24h) resulted in markedly elevated contractile responses to the Tx analog U46619, compared with the control DMSO. There was no increase in TP receptor mRNA expression, while the protein expression was significantly enhanced. This up-regulation was not affected by a general transcriptional inhibitor actinomycin D, but was almost completely abolished by cycloheximide, a general translational inhibitor. Dexamethasone, a glucocorticoid, manifested a potent inhibitory effect as well. These results suggest that the up-regulation of TP receptor occurs via post-transcriptional events, and mainly translation. This is supported by experiments with specific inhibitors for c-Jun-NH(2)-terminal kinase (SP600125), extracellular signal-regulated kinase 1 and 2 (PD98059 and U0126) and p38 (SB203580) that had no inhibitory effect on the up-regulation of TP receptors. Collectively, the results show that MAPK pathways are not involved in TP receptor up-regulation. Study on TP receptor mRNA stability showed that during organ culture, the TP receptor mRNA was stable in both DMSO and DSP group, but the latter elicited a tendency to stabilize the TP receptor mRNA at higher level. Thus, post-transcriptional mechanisms are responsible for the up-regulation of TP receptor by DSP, in which enhanced translation is the major cause of the elevated protein expression and the enhanced contraction.

    Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Publishing Authors By Initials

    w zhangW Zhang,y zhangY Zhang,l edvinssonL Edvinsson,cb xuCB Xu,w zhangW Zhang,y zhangY Zhang,l edvinssonL Edvinsson,cb xuCB Xu,

    For similar abstracts research abstracts see: abstracts research

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    Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Atherosclerosis

    VOLUME: 196

    Page Numbers: 608-16

    Journal Abbreviation: Atherosclerosis

    ISSN: 1879-1484

    DAY: 13

    MONTH: 08

    YEAR: 2007

    Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Information

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    LANGUAGE: eng

    NlmUniqueID: 242543

    Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms. Keywords Mesh Terms:

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    Grant and Affiliation Information for Up-regulation of thromboxane A2 receptor expression by lipid soluble smoking particles through post-transcriptional mechanisms.

    AFFILIATION: Division of Experimental Vascular Research, Institute of Clinical Science in Lund, Lund University, Lund, Sweden.

    Country: Ireland

    Ireland Research PublicationIreland Research Publication

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    MEDLINETA: Atherosclerosis

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