Kaufmann U, Kirsch J, Irintchev A, Wernig A, Starzinski-Powitz A
Institut der Anthropologie und Humangenetik fuer Biologen, Johann-Wolfgang-Goethe-Universitaet Frankfurt, Siesmayerstrasse 70, D-60054 Frankfurt/Main, Germany.
J Cell Sci. 1999 Jan;112 ( Pt 1):55-68. doi: 10.1242/jcs.112.1.55.
M-cadherin, a calcium-dependent intercellular adhesion molecule, is expressed in skeletal muscle cells. Its pattern of expression, both in vivo and in cell culture as well as functional studies, have implied that M-cadherin is important for skeletal muscle development, in particular the fusion of myoblasts into myotubes. M-cadherin formed complexes with the catenins in skeletal muscle cells similar to E-cadherin in epithelial cells. This suggested that the muscle-specific function of the M-cadherin catenin complex might be mediated by additional interactions with yet unidentified cellular components, especially cytoskeletal elements. These include the microtubules which also have been implicated in the fusion process of myoblasts. Here we present evidence that the M-cadherin catenin complex interacts with microtubules in myogenic cells by using three independent experimental approaches. (1) Analysis by laser scan microscopy revealed that the destruction of microtubules by nocodazole leads to an altered cell surface distribution of M-cadherin in differentiating myogenic cells. In contrast, disruption of actin filaments had little effect on the surface distribution of M-cadherin. (2) M-cadherin antibodies coimmunoprecipitated tubulin from extracts of nocodazole-treated myogenic cells but not of nocodazole-treated epithelial cells ectopically expressing M-cadherin. Vice versa, tubulin antibodies coimmunoprecipitated M-cadherin from extracts of nocodazole-treated myogenic cells but not of nocodazole-treated M-cadherin-expressing epithelial cells. (3) M-cadherin and the catenins, but not a panel of control proteins, were copolymerized with tubulin from myogenic cell extracts even after repeated cycles of assembly and disassemly of tubulin. Moreover, neither M-cadherin nor E-cadherin could be found in a complex with microtubules in epithelial cells ectopically expressing M-cadherin. Our data are consistent with the idea that the interaction of M-cadherin with microtubules might be essential to keep the myoblasts aligned during fusion, a process in which both M-cadherin and microtubules have been implicated.
M-钙黏蛋白是一种钙依赖性细胞间黏附分子,在骨骼肌细胞中表达。其在体内、细胞培养中的表达模式以及功能研究均表明,M-钙黏蛋白对骨骼肌发育很重要,尤其是对成肌细胞融合形成肌管的过程。M-钙黏蛋白在骨骼肌细胞中与连环蛋白形成复合物,类似于上皮细胞中的E-钙黏蛋白。这表明M-钙黏蛋白连环蛋白复合物的肌肉特异性功能可能是由与尚未确定的细胞成分(尤其是细胞骨架成分)的额外相互作用介导的。这些成分包括微管,微管也与成肌细胞的融合过程有关。在此,我们通过三种独立的实验方法提供证据表明,M-钙黏蛋白连环蛋白复合物在成肌细胞中与微管相互作用。(1)激光扫描显微镜分析显示,诺考达唑破坏微管会导致分化中的成肌细胞中M-钙黏蛋白的细胞表面分布发生改变。相比之下,肌动蛋白丝的破坏对M-钙黏蛋白的表面分布影响很小。(2)M-钙黏蛋白抗体从诺考达唑处理的成肌细胞提取物中共同免疫沉淀微管蛋白,但不能从异位表达M-钙黏蛋白的诺考达唑处理的上皮细胞提取物中沉淀。反之亦然,微管蛋白抗体从诺考达唑处理的成肌细胞提取物中共同免疫沉淀M-钙黏蛋白,但不能从诺考达唑处理的表达M-钙黏蛋白的上皮细胞提取物中沉淀。(3)即使在微管蛋白反复组装和拆卸循环后,M-钙黏蛋白和连环蛋白,而非一组对照蛋白,仍与成肌细胞提取物中的微管蛋白共聚。此外,在异位表达M-钙黏蛋白的上皮细胞中,未发现M-钙黏蛋白和E-钙黏蛋白与微管形成复合物。我们的数据与以下观点一致,即M-钙黏蛋白与微管的相互作用可能对融合过程中成肌细胞的排列至关重要,在这个过程中M-钙黏蛋白和微管都参与其中。