Zádor Erno, Fenyvesi Rita, Wuytack Frank
Institute of Biochemistry, Faculty of Medicine, Albert Szent-Györgyi Medical and Pharmaceutical Center, University of Szeged, BOBox 427, Dóm tér 9, H-6701 Szeged, Hungary.
FEBS Lett. 2005 Jan 31;579(3):749-52. doi: 10.1016/j.febslet.2004.12.061.
This study investigates to what extent the expression of the slow myosin heavy chain (MyHCI) isoform and the slow type sarcoplasmic reticulum Ca2+ ATPase (SERCA2a) isoform are co-regulated in fibers of regenerating skeletal soleus muscle. Both overexpression of cain, a calcineurin inhibitor, or partial tenotomy prevented the expression of MyHCI but left SERCA2a expression unaffected in fibers of regenerating soleus muscles. These data complement those from different experimental models and clearly show that the expression of MyHCI and SERCA2a--the major proteins mediating, respectively, the slow type of contraction and relaxation--are not coregulated in regenerating soleus muscle.
本研究调查了再生比目鱼肌纤维中慢肌球蛋白重链(MyHCI)亚型和慢型肌浆网Ca2+ATP酶(SERCA2a)亚型的表达在多大程度上受到共同调节。钙调神经磷酸酶抑制剂cain的过表达或部分肌腱切断术均可阻止MyHCI的表达,但对再生比目鱼肌纤维中SERCA2a的表达没有影响。这些数据补充了来自不同实验模型的数据,并清楚地表明,MyHCI和SERCA2a(分别介导慢型收缩和舒张的主要蛋白质)的表达在再生比目鱼肌中不受共同调节。