Redox Regulation of Ion Channels in the Pulmonary Circulation

被引:30
|
作者
Olschewski, Andrea [1 ,2 ]
Weir, Edward Kenneth [3 ]
机构
[1] Ludwig Boltzmann Inst Lung Vasc Res, A-8010 Graz, Austria
[2] Med Univ Graz, Dept Anesthesia & Intens Care Med, Graz, Austria
[3] Univ Minnesota, Dept Med, VA Med Ctr, Minneapolis, MN 55455 USA
关键词
VASCULAR SMOOTH-MUSCLE; GATED K+ CHANNELS; HYPOXIC HUMAN PULMONARY; KCNQ POTASSIUM CHANNELS; NITRIC-OXIDE; S-NITROSYLATION; HYDROGEN-PEROXIDE; OXIDATIVE STRESS; TYROSINE KINASE; CA2+ RESPONSES;
D O I
10.1089/ars.2014.5899
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Significance: The pulmonary circulation is a low-pressure, low-resistance, highly compliant vasculature. In contrast to the systemic circulation, it is not primarily regulated by a central nervous control mechanism. The regulation of resting membrane potential due to ion channels is of integral importance in the physiology and pathophysiology of the pulmonary vasculature. Recent Advances: Redox-driven ion conductance changes initiated by direct oxidation, nitration, and S-nitrosylation of the cysteine thiols and indirect phosphorylation of the threonine and serine residues directly affect pulmonary vascular tone. Critical Issues: Molecular mechanisms of changes in ion channel conductance, especially the identification of the sites of action, are still not fully elucidated. Future Directions: Further investigation of the interaction between redox status and ion channel gating, especially the physiological significance of S-glutathionylation and S-nitrosylation, could result in a better understanding of the physiological and pathophysiological importance of these mediators in general and the implications of such modifications in cellular functions and related diseases and their importance for targeted treatment strategies. Antioxid. Redox Signal. 22, 465-485.
引用
收藏
页码:465 / 485
页数:21
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