National Research Laboratory for Mitochondrial Signaling, Department of Physiology, College of Medicine, Cardiovascular and Metabolic Disease Center, FIRST Mitochondrial Research Group, Inje University, 633-165 Gaegeum-dong, Busanjin-gu, Busan 614-735, Republic of Korea.
Prog Biophys Mol Biol. 2010 Sep;103(1):95-101. doi: 10.1016/j.pbiomolbio.2009.10.001. Epub 2009 Oct 14.
In this review, the pathological alteration and clinical relevance of voltage-gated K(+) (Kv) channels and their specific regulation by protein kinase-dependent signaling in vascular smooth muscle cells are described, particularly focusing on the pulmonary vasculature. The physiological relevance, channel characteristics, pharmacological modulation, and expression of Kv channels vary between different arterial beds and between subdivisions of arteries within those vascular beds. Although detailed signaling cascades regulating Kv channels are not clearly elucidated, it is known that the Kv channels in vascular smooth muscle cells can be tightly regulated by protein kinases C (PKC) and A (PKA). Alterations in Kv channel expression and function has been noted in pathological and pathophysiological conditions including hypertension (pulmonary and systemic), in diabetes and in individuals subjected to prolonged hypoxia (high altitude living). Vascular Kv channels are potential therapeutic targets in diseases such as pulmonary arterial hypertension and, therefore, it is important to understand the specific pharmacological modulation of Kv channel isoforms in different vascular beds.
在这篇综述中,描述了电压门控 K(+)(Kv)通道的病理改变和临床相关性,以及它们在血管平滑肌细胞中通过蛋白激酶依赖性信号的特定调节,特别是重点关注肺血管。不同的动脉床和这些血管床内的动脉分支之间,Kv 通道的生理相关性、通道特性、药理学调节和表达都有所不同。尽管详细的调节 Kv 通道的信号级联尚未明确阐明,但已知血管平滑肌细胞中的 Kv 通道可以被蛋白激酶 C(PKC)和 A(PKA)紧密调节。在包括高血压(肺和全身)、糖尿病和长期缺氧(高海拔生活)在内的病理和病理生理条件下,已经注意到 Kv 通道表达和功能的改变。血管 Kv 通道是肺动脉高压等疾病的潜在治疗靶点,因此,了解不同血管床中 Kv 通道同工型的特定药理学调节非常重要。