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HIF-1alpha overexpression and experimental murine atherosclerosis.

机译:HIF-1alpha过表达和实验性小鼠动脉粥样硬化。

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BACKGROUND: Lymphocytes play an important role in the progression of atherosclerosis. Recently, hypoxia inducible factor-1 (HIF-1) was found to attenuate inflammation by regulating T cell activation and cytokine production. We studied the effects of overexpression of HIF-1alpha in ApoE knockout murine lymphocytes, on experimental atherosclerosis. METHODS AND RESULTS: ApoE-/- mice were submitted to intravenous hydrodynamic injection of empty plasmid or HIF-1alphaP564A (HIF-1alpha mutated stabilized construct). Robust expression of HIF-1alpha was evident in spleen cells of recipient animals. Increased expression of IL-10 as well as decreased expression of IFN-gamma was measured in splenocytes of HIF-1alpha-treated mice by RT-PCR. One week postinjection, antibody array analysis revealed a pattern consistent with a T helper 1 to T helper 2 shift. On sacrifice, assessment of aortic sinus lesions revealed a significant reduction in plaque size in HIF-1alpha injected mice. A reduced expression of IFN-gamma was evident in CD4+ spleen-derived lymphocytes and aortas of HIF-1alpha-injected mice. CONCLUSIONS: HIF-1alpha expression in mouse lymphocytes is associated with a reduced IFN-gamma expression and attenuation of experimental atherosclerosis.
机译:背景:淋巴细胞在动脉粥样硬化的进展中起重要作用。最近,发现缺氧诱导因子-1(HIF-1)通过调节T细胞活化和细胞因子产生来减轻炎症。我们研究了ApoE基因敲除小鼠淋巴细胞中HIF-1alpha的过表达对实验性动脉粥样硬化的影响。方法和结果:ApoE-/-小鼠被静脉注射空质粒或HIF-1alphaP564A(HIF-1alpha突变的稳定构建体)进行流体动力注射。在受体动物的脾细胞中,HIF-1alpha的表达很强。通过RT-PCR测定了HIF-1alpha处理的小鼠脾细胞中IL-10的表达增加以及IFN-γ的表达减少。注射后一周,抗体阵列分析显示出与T辅助1到T辅助2转变一致的模式。处死后,对主动脉窦病变的评估显示在注射HIF-1alpha的小鼠中斑块大小显着减少。在注射了HIF-1α的小鼠的CD4 +脾脏淋巴细胞和主动脉中,IFN-γ的表达降低。结论:小鼠淋巴细胞中的HIF-1alpha表达与IFN-γ表达降低和实验性动脉粥样硬化的减弱有关。

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