Department of Cell and Developmental Biology, Institute of Biomedical Sciences, University of Sao Paulo, Lineu Prestes Av., 1524, 05508-900 Sao Paulo, SP, Brazil.
J Struct Biol. 2010 May;170(2):344-53. doi: 10.1016/j.jsb.2010.02.001. Epub 2010 Feb 10.
MuRF1 is a member of the RBCC (RING, B-box, coiled-coil) superfamily that has been proposed to act as an atrogin during muscle wasting. Here, we show that MuRF1 is preferentially induced in type-II muscle fibers after denervation. Fourteen days after denervation, MuRF1 protein was further elevated but remained preferentially expressed in type-II muscle fibers. Consistent with a fiber-type dependent function of MuRF1, the tibialis anterior muscle (rich in type-II muscle fibers) was considerably more protected in MuRF1-KO mice from muscle wasting when compared to soleus muscle with mixed fiber-types. We also determined fiber-type distributions in MuRF1/MuRF2 double-deficient KO (dKO) mice, because MuRF2 is a close homolog of MuRF1. MuRF1/MuRF2 dKO mice showed a profound loss of type-II fibers in soleus muscle. As a potential mechanism we identified the interaction of MuRF1/MuRF2 with myozenin-1, a calcineurin/NFAT regulator and a factor required for maintenance of type-II muscle fibers. MuRF1/MuRF2 dKO mice had lost myozenin-1 expression in tibialis anterior muscle, implicating MuRF1/MuRF2 as regulators of the calcineurin/NFAT pathway. In summary, our data suggest that expression of MuRF1 is required for remodeling of type-II fibers under pathophysiological stress states, whereas MuRF1 and MuRF2 together are required for maintenance of type-II fibers, possibly via the regulation of myozenin-1.
肌萎缩蛋白 1(MuRF1)是 RBCC(RING、B 盒、卷曲螺旋)超家族的成员,据推测其在肌肉减少症中充当肌萎缩蛋白。在这里,我们表明 MuRF1 在去神经后优先诱导 II 型肌纤维。去神经后 14 天,MuRF1 蛋白进一步升高,但仍优先在 II 型肌纤维中表达。与 MuRF1 的纤维类型依赖性功能一致,比目鱼肌(富含 II 型肌纤维)在 MuRF1-KO 小鼠中从肌肉减少症中得到了更大的保护,而比目鱼肌则具有混合纤维类型。我们还确定了 MuRF1/MuRF2 双缺失 KO(dKO)小鼠中的纤维类型分布,因为 MuRF2 是 MuRF1 的密切同源物。MuRF1/MuRF2 dKO 小鼠在比目鱼肌中出现 II 型纤维的严重丧失。作为一种潜在的机制,我们鉴定了 MuRF1/MuRF2 与肌联蛋白-1 的相互作用,肌联蛋白-1 是一种钙调神经磷酸酶/NFAT 调节剂,也是维持 II 型肌纤维所必需的因子。MuRF1/MuRF2 dKO 小鼠在前臂肌中失去了肌联蛋白-1 的表达,这表明 MuRF1/MuRF2 是钙调神经磷酸酶/NFAT 途径的调节剂。总之,我们的数据表明,在病理生理应激状态下,MuRF1 的表达是 II 型纤维重塑所必需的,而 MuRF1 和 MuRF2 一起是 II 型纤维维持所必需的,可能通过调节肌联蛋白-1 来实现。