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Reduced intracellular chloride concentration impairs angiogenesis by inhibiting oxidative stress-mediated VEGFR2 activation

   
@article{APS10299,
	author = {Kai Li and Ying-ying Liu and Xiao-fei Lv and Zhuo-miao Lin and Ting-ting Zhang and Fei-ran Zhang and Jia-wei Guo and Yu Hong and Xiu Liu and Xiao-chun Lin and Jia-guo Zhou and Qian-qian Wu and Si-jia Liang and Jin-yan Shang},
	title = {Reduced intracellular chloride concentration impairs angiogenesis by inhibiting oxidative stress-mediated VEGFR2 activation},
	journal = {Acta Pharmacologica Sinica},
	volume = {42},
	number = {4},
	year = {2021},
	keywords = {},
	abstract = {Chloride (Cl−) homeostasis is of great significance in cardiovascular system. Serum Cl− level is inversely associated with the mortality of patients with heart failure. Considering the importance of angiogenesis in the progress of heart failure, this study aims to investigate whether and how reduced intracellular Cl− concentration ([Cl−]i) affects angiogenesis. Human umbilical endothelial cells (HUVECs) were treated with normal Cl− medium or low Cl− medium. We showed that reduction of [Cl−]i (from 33.2 to 16.18 mM) inhibited HUVEC proliferation, migration, cytoskeleton reorganization, tube formation, and subsequently suppressed angiogenesis under basal condition, and VEGF stimulation or hypoxia treatment. Moreover, VEGF-induced NADPH-mediated reactive oxygen species (ROS) generation and VEGFR2 axis activation were markedly attenuated in low Cl− medium. We revealed that lowering [Cl−]i inhibited the expression of the membrane-bound catalytic subunits of NADPH, i.e., p22phox and Nox2, and blunted the translocation of cytosolic regulatory subunits p47phox and p67phox, thereby restricting NADPH oxidase complex formation and activation. Furthermore, reduced [Cl−]i enhanced ROS-associated protein tyrosine phosphatase 1B (PTP1B) activity and increased the interaction of VEGFR2 and PTP1B. Pharmacological inhibition of PTP1B reversed the effect of lowering [Cl−]i on VEGFR2 phosphorylation and angiogenesis. In mouse hind limb ischemia model, blockade of Cl− efflux using Cl− channel inhibitors DIDS or DCPIB (10 mg/kg, i.m., every other day for 2 weeks) significantly enhanced blood flow recovery and new capillaries formation. In conclusion, decrease of [Cl−]i suppresses angiogenesis via inhibiting oxidase stress-mediated VEGFR2 signaling activation by preventing NADPH oxidase complex formation and promoting VEGFR2/PTP1B association, suggesting that modulation of [Cl−]i may be a novel therapeutic avenue for the treatment of angiogenic dysfunction-associated diseases.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/10299}
}