Bönnemann C G, Thompson T G, van der Ven P F M, Goebel H H, Warlo I, Vollmers B, Reimann J, Herms J, Gautel M, Takada F, Beggs A H, Fürst D O, Kunkel L M, Hanefeld F, Schröder R
Division of Neurology, Children's Hospital of Philadelphia and University of Pennsylvania School of Medicine, 34th Strteet and Civic Center Boulevard, Philadelphia, PA 19104, USA.
J Neurol Sci. 2003 Jan 15;206(1):71-8. doi: 10.1016/s0022-510x(02)00341-6.
Filamin C is the muscle isoform of a group of large actin-crosslinking proteins. On the one hand, filamin C is associated with the Z-disk of the myofibrillar apparatus and binds to myotilin; on the other hand, it interacts with the sarcoglycan complex at the sarcolemma. Filamin C may be involved in reorganizing the cytoskeleton in response to signalling events and in muscle it may, in addition, fulfill structural functions at the Z-disk. An examination of biopsies from patients with multi-minicore myopathy, central core myopathy and neurogenic target fibers with core-like target formations (TF) revealed strong reactivity of all the cores and target formations with two different anti-filamin C antibodies. In all three conditions, the immunoreactivity in the cores for filamin C was considerably stronger than that for desmin. Only for alphaB-crystallin were comparable levels of immunoreactivity detected. There was no difference in intensity for filamin C between the three pathological conditions. Thus, filamin C along with alphaB-crystallin is a strong and robust, but nonspecific marker of core formation. The reason why filamin C accumulates in cores is unclear at present, but we postulate that it may be critically involved in the chain of events eventually leading to myofibrillar degeneration.
细丝蛋白C是一组大型肌动蛋白交联蛋白的肌肉异构体。一方面,细丝蛋白C与肌原纤维装置的Z盘相关联,并与肌联蛋白结合;另一方面,它在肌膜处与肌聚糖复合体相互作用。细丝蛋白C可能参与响应信号事件而对细胞骨架进行重组,并且在肌肉中,它还可能在Z盘处发挥结构功能。对患有多微小核肌病、中央核肌病和具有核心样靶形(TF)的神经源性靶纤维患者的活检样本进行检查发现,所有的核和靶形对两种不同的抗细丝蛋白C抗体均表现出强反应性。在所有这三种情况下,核中细丝蛋白C的免疫反应性明显强于结蛋白。仅αB晶状体蛋白检测到了相当水平的免疫反应性。三种病理状况之间细丝蛋白C的强度没有差异。因此,细丝蛋白C与αB晶状体蛋白一起是核心形成的一种强大且可靠但非特异性的标志物。目前尚不清楚细丝蛋白C在核中积累的原因,但我们推测它可能在最终导致肌原纤维变性的一系列事件中起关键作用。