Boncompagni Simona, Protasi Feliciano, Franzini-Armstrong Clara
IIM-Interuniversitary Institute of Myology, DNI-Department of Neuroscience and Imaging, CeSI-Centro Scienze dell'Invecchiamento, Università degli Studi G. d'Annunzio, 66013, Chieti, Italy.
Age (Dordr). 2012 Feb;34(1):27-41. doi: 10.1007/s11357-011-9211-y. Epub 2011 Feb 12.
Tubular aggregates (TAs), ordered arrays of elongated sarcoplasmic reticulum (SR) tubules, are present in skeletal muscle from patients with myopathies and are also experimentally induced by extreme anoxia. In wild-type mice TAs develop in a clear age-, sex- (male), and fiber type- (fast twitch) dependence. However, the events preceding the appearance of TAs have not been explored. We investigated the sequential stages leading to the initial appearance and maturation of TAs in EDL from male mice. TAs' formation requires two temporally distinct steps that operate via different mechanisms. Initially (before 1 year of age), the SR Ca(2+) binding protein calsequestrin (CASQ) accumulates specifically at the I band level causing swelling of free SR cisternae. In the second stage, the enlarged SR sacs at the I band level extend into multiple, longitudinally oriented tubules with a full complement of sarco(endo)plasmic reticulum Ca(2+) ATPases (SERCA) in the membrane and CASQ in the lumen. Tubules gradually acquire a regular cylindrical shape and uniform size apparently in concert with partial crystallization of SERCA. Multiple, small TAs associate to form fewer mature TAs of very large size. Interestingly, in fibers from CASQ1-knockout mice abnormal aggregates of SR tubules have different conformation and never develop into ordered aggregates of straight cylinders, possibly due to lack of CASQ accumulation. We conclude that TAs do not arise abruptly but are the final result of a gradually changing SR architecture and we suggest that the crystalline ATPase within the aggregates may be inactive.
管状聚集体(TAs)是由细长的肌浆网(SR)小管有序排列而成,存在于患有肌病患者的骨骼肌中,也可通过极端缺氧实验诱导产生。在野生型小鼠中,TAs的形成明显依赖于年龄、性别(雄性)和纤维类型(快肌纤维)。然而,TAs出现之前的事件尚未得到探索。我们研究了雄性小鼠趾长伸肌(EDL)中TAs最初出现和成熟的连续阶段。TAs的形成需要两个时间上不同的步骤,通过不同的机制运作。最初(1岁之前),SR钙结合蛋白肌集钙蛋白(CASQ)特异性地在I带水平积累,导致游离SR池肿胀。在第二阶段,I带水平增大的SR囊延伸成多个纵向排列的小管,其膜上有完整的肌质网钙ATP酶(SERCA),管腔内有CASQ。小管逐渐形成规则的圆柱形和均匀的大小,显然与SERCA的部分结晶一致。多个小的TAs结合形成较少的非常大的成熟TAs。有趣的是,在来自CASQ1基因敲除小鼠的纤维中,SR小管的异常聚集体具有不同的构象,并且从未发展成直圆柱体的有序聚集体,这可能是由于缺乏CASQ积累。我们得出结论,TAs不是突然出现的,而是SR结构逐渐变化的最终结果,并且我们认为聚集体内的结晶ATP酶可能是无活性的。