Emerging role of PKA/eNOS pathway in therapeutic angiogenesis for ischaemic tissue diseases

被引:96
作者
Bir, Shyamal C. [2 ]
Xiong, Yan [1 ]
Kevil, Christopher G. [2 ]
Luo, Jincai [1 ]
机构
[1] Peking Univ, Inst Mol Med, Lab Vasc Biol, Beijing 100871, Peoples R China
[2] LSU Hlth Sci Ctr Shreveport, Dept Pathol, Shreveport, LA USA
关键词
PKA; eNOS; Nitric oxide; Nitrite; Vascular remodelling; NITRIC-OXIDE-SYNTHASE; ENDOTHELIAL GROWTH-FACTOR; PROTEIN-KINASE-A; VASCULAR SMOOTH-MUSCLE; STRESS STIMULATES PHOSPHORYLATION; PROGENITOR-CELL MOBILIZATION; REACTIVE OXYGEN; OXIDATIVE STRESS; SHEAR-STRESS; IN-VITRO;
D O I
10.1093/cvr/cvs143
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although an abundant amount of research has been devoted to the study of angiogenesis, its precise mechanisms are incompletely understood. Numerous clinical trials focused on therapeutic angiogenesis for the treatment of tissue ischaemia have not been as successful as those of preclinical studies. Thus, additional studies are needed to better understand critical molecular mechanisms regulating ischaemic neovascularization to identify novel therapeutic agents. Nitric oxide (NO) plays a central role in ischaemic neovascularization through the generation of cyclic guanosine monophosphate (cGMP) and the activation of several other signalling responses. Accumulated evidence suggests that endothelial protein kinase A/endothelial NO synthase (PKA/eNOS) signalling may play an important role in ischaemic disorders by promoting neovascularization. This review highlights recent advances in the role of the PKA/eNOS and NO-cGMP-kinase cascade pathway in ischaemic neovascularization. We also discuss molecular relationships of PKA/eNOS with other angiogenic pathways and explore the possibility of activation of the NO/nitrite endocrine system as potential therapeutic targets for ischaemic angiogenesis.
引用
收藏
页码:7 / 18
页数:12
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