Differential responsiveness in VEGF receptor subtypes to hypoxic stress in various tissues of plateau animals
Language English Country Czech Republic Media print-electronic
Document type Comparative Study, Journal Article
PubMed
27982675
DOI
10.33549/physiolres.933408
PII: 933408
Knihovny.cz E-resources
- MeSH
- Acclimatization MeSH
- Species Specificity MeSH
- Hypoxia-Inducible Factor 1, alpha Subunit metabolism MeSH
- Stress, Physiological MeSH
- Hypoxia metabolism MeSH
- Muscle, Skeletal metabolism MeSH
- Lagomorpha metabolism MeSH
- Myocardium metabolism MeSH
- Altitude MeSH
- Organ Specificity physiology MeSH
- Lung metabolism MeSH
- Rats, Sprague-Dawley MeSH
- Receptors, Vascular Endothelial Growth Factor metabolism MeSH
- Gene Expression Regulation physiology MeSH
- Tissue Distribution MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Geographicals
- Tibet MeSH
- Names of Substances
- Hypoxia-Inducible Factor 1, alpha Subunit MeSH
- Receptors, Vascular Endothelial Growth Factor MeSH
With hypoxic stress, hypoxia-inducible factor-1alpha (HIF-1alpha) and vascular 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-1alpha 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-1alpha and the protein expression of VEGFRs in control animals and plateau pikas. We further blocked HIF-1alpha signal to determine if HIF-1alpha 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-1alpha. 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 observed decreases of VEGFR-2 in skeletal muscle, heart and lung; and decreases of VEGFR-3 in lung following HIF-1alpha 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 observed in lung; 3) HIF-1alpha 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.
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