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首页> 外文期刊>Physiological Research >Differential responsiveness in VEGF receptor subtypes to hypoxic stress in various tissues of plateau animals.
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Differential responsiveness in VEGF receptor subtypes to hypoxic stress in various tissues of plateau animals.

机译:在高原动物的各种组织中,VEGF受体亚型对低氧应激的差异反应。

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With hypoxic stress, hypoxia-inducible factor-1α (HIF-1α) and vas cular endothelial growth factor (VEGF) are elevated and their responses are altered in skeletal muscles of plateau animals [China Qinghai-Tibetan plateau pikas (Ochotona curzoniae)] as compared with control animals [normal lowland Sprague-Dawley (SD) rats]. The results indicate that HIF-1α and VEGF are engaged in physiological functions under hypoxic environment. The purpose of the current study was to examine the protein levels of VEGF receptor subtypes (VEGFRs: VEGFR-1, VEGFR-2 and VEGFR -3) in the end organs, namely skeletal muscle, heart and lung in response to hypoxic stress. ELISA and Western blot analysis were employed to determine HIF-1α and the protein expression of VEGFRs in control animals and plateau pikas. We further blocked HIF-1α signal to determine if HIF-1α regulates alternations in VEGFRs in those tissues. We hypothesized that responsiveness of VEGFRs in the major end organs of plateau animals is differential with insult of hypoxic stress and is modulated by low oxygen sensitive HIF-1α. Our results show that hypoxic stress induced by exposure of lower O 2 for 6 h significantly increased the levels of VEGFR -2 in skeletal muscle, heart and lung and the increases were amplified in plateau pikas. Our results also demonstrate that hypoxic stress enhanced VEGFR -3 in lungs of plateau animals. Nonetheless, no significant alternations in VEGFR -1 were observed in those tissues with hypoxic stress. Moreover, we obs erved decreases of VEGFR-2 in skeletal muscle, heart and lung; and decreases of VEGFR-3 in lung following HIF-1α inhibition. Overall, our findings suggest that in plateau animals 1) responsiveness of VEGFRs is different under hypoxic environment; 2) amplified VEGFR-2 response appears in skeletal muscle, heart and lung, and enhanced VEGFR-3 response is mainly obs erved in lung; 3) HIF-1α plays a regulatory role in the levels of VEGFRs. Our results provide the underlying cellular and molecular mechanisms responsible for hypoxic environment in plateau animals, having an impact on research of physiological and ecological adaptive responses to acute or chronic hypoxic stress in humans who living at high attitude and who live at a normal sea level but suffer from hypoxic disorders.
机译:在低氧胁迫下,高原动物[中国青藏高原鼠兔(Ochotona curzoniae)]的缺氧诱导因子-1α(HIF-1α)和血管内皮生长因子(VEGF)升高,其反应发生改变。与对照组动物比较[正常低地Sprague-Dawley(SD)大鼠]。结果表明,HIF-1α和VEGF在缺氧环境下均参与生理功能。本研究的目的是检查响应低氧应激的终末器官,即骨骼肌,心脏和肺中VEGF受体亚型(VEGFRs:VEGFR-1,VEGFR-2和VEGFR -3)的蛋白水平。 ELISA和蛋白质印迹分析被用于确定对照动物和高原鼠兔中的HIF-1α和VEGFRs的蛋白表达。我们进一步阻断了HIF-1α信号,以确定HIF-1α是否调节那些组织中VEGFR的交替。我们假设高原动物主要末端器官中的VEGFRs反应性与低氧应激的损伤是不同的,并且受低氧敏感性HIF-1α的调节。我们的结果表明,较低的O 2暴露6 h引起的低氧应激显着增加了骨骼肌,心脏和肺中VEGFR -2的水平,高原鼠兔中的这种升高被放大。我们的结果还表明,低氧应激会增强高原动物肺部的VEGFR -3。但是,在低氧应激的组织中未观察到VEGFR -1的显着变化。此外,我们观察到骨骼肌,心脏和肺中VEGFR-2的减少。 HIF-1α抑制后肺中VEGFR-3降低。总体而言,我们的发现表明,在高原动物中:1)低氧环境下VEGFR的反应性不同; 2)在骨骼肌,心脏和肺中出现了扩增的VEGFR-2反应,而在肺中主要观察到了增强的VEGFR-3反应。 3)HIF-1α在VEGFRs水平中起调节作用。我们的研究结果为高原动物的低氧环境提供了潜在的细胞和分子机制,影响了对高姿态和正常海平面的人急性或慢性低氧应激的生理和生态适应性反应的研究。患有缺氧性疾病。

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