Kumar C, Saidapet C, Delaney P, Mendola C, Siddiqui M A
Roche Institute of Molecular Biology, Roche Research Center, Nutley, New Jersey.
Circ Res. 1988 Jun;62(6):1093-7. doi: 10.1161/01.res.62.6.1093.
Using cloned DNA probes specific for two isoforms of cardiac myosin light chains (MLCs), nonphosphorylatable MLC1 and phosphorylatable, regulatory MLC2, we have observed that the MLC1 messenger RNA of ventricular type does not appear in detectable amounts in atrial cells of either normotensive Wistar-Kyoto rat strain (WKY) or spontaneously hypertensive rat strain (SHR). The messenger RNA of regulatory isoform of ventricular MLC2, on the other hand, is found in threefold excess in atria of SHR relative to that of age-matched WKY. The increased level of MLC2 messenger RNA is present even in 6-week-old SHR atria where there is no established overloading of the heart. Thus, it appears that the increased expression of the regulatory MLC2 gene in SHR atrial cells is a predetermined event, which, most likely, participates in functional adaptation of the myocardium in response to pressure overload and subsequent hypertrophy.
利用针对心肌肌球蛋白轻链(MLCs)的两种同工型——非磷酸化的MLC1和可磷酸化的调节性MLC2的克隆DNA探针,我们观察到,在正常血压的Wistar-Kyoto大鼠品系(WKY)或自发性高血压大鼠品系(SHR)的心房细胞中,未检测到心室型MLC1信使核糖核酸(mRNA)的存在。另一方面,在SHR心房中发现,心室MLC2调节同工型的信使核糖核酸比年龄匹配的WKY心房中的多三倍。即使在6周龄的SHR心房中,心脏尚未出现明显的负荷过重时,MLC2信使核糖核酸水平也会升高。因此,似乎SHR心房细胞中调节性MLC2基因表达的增加是一个预先确定的事件,这很可能参与了心肌对压力超负荷和随后的肥大的功能适应。