Ke Yunbo, Lei Ming, Wang Xin, Solaro R John
Department of Physiology and Biophysics and Center for Cardiovascular Research; University of Illinois at Chicago; Chicago, IL USA.
Cell Logist. 2012 Apr 1;2(2):89-94. doi: 10.4161/cl.21497.
Our work and others' over the past few years have led to the identification of new roles of PAK1 in cardiac physiology, such as the regulation of cardiac ion channel and actomyosin function. More recent studies have revealed that PAK1-deficient mice were vulnerable to cardiac hypertrophy and readily progress to failure under sustained pressure overload and susceptible to ischemia/reperfusion injury. Our further study indicated that the PAK1 activator FTY720 was able to prevent this pressure overload-induced hypertrophy in wild-type mice without compromising their cardiac functions. A cardiac protective effect against ischemia/reperfusion injury by FTY720 was also observed in both rat and mouse models by us and others. Thus, these studies suggest that PAK1 is more important in the heart than previously thought, in particular a therapeutic potential of PAK1 activators. In the future, in-depth investigations are required to further substantiate our hypotheses on mechanisms for PAK1 function in the heart and to explore a therapeutic potential of FTY720 and other PAK1 activators in heart disease conditions.
在过去几年里,我们以及其他人的研究工作已促成了对PAK1在心脏生理学中的新作用的识别,比如对心脏离子通道和肌动球蛋白功能的调节。最近的研究表明,PAK1基因缺陷型小鼠易患心脏肥大,在持续压力超负荷情况下很容易发展为心力衰竭,并且易受缺血/再灌注损伤影响。我们进一步的研究表明,PAK1激活剂FTY720能够在不损害野生型小鼠心脏功能的情况下预防这种压力超负荷诱导的肥大。我们和其他人在大鼠和小鼠模型中也观察到了FTY720对缺血/再灌注损伤的心脏保护作用。因此,这些研究表明,PAK1在心脏中的重要性比之前认为的更高,尤其是PAK1激活剂具有治疗潜力。未来,需要进行深入研究以进一步证实我们关于PAK1在心脏中功能机制的假设,并探索FTY720和其他PAK1激活剂在心脏病情况下的治疗潜力。