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Journal of experimental & biomedical sciences = 대한의생명과학회지 v.13 no.4, 2007년, pp.251 - 261  
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Knockdown of Archvillin by siRNA Inhibits Myofibril Assembly in Cultured Skeletal Myoblast

Lee, Yeong-Mi   (Department of Biomedical Laboratory Science, Inje UniversityUU0001067  ); Kim, Hyun-Suk   (Department of Biomedical Laboratory Science, Inje UniversityUU0001067  ); Choi, Jun-Hyuk   (Department of Biomedical Laboratory Science, Inje UniversityUU0001067  ); Choi, Jae-Kyoung   (Department of Biology, Graduate School, Inje UniversityUU0001067  ); Joo, Young-Mi   (Team of BK21, Center of Smart Foods and Drugs, Inje UniversityUU0001067  ); Ahn, Seung-Ju   (Department of Clinical Pathology, Daegu Health Collage  ); Min, Byung-In   (Department of Radiation Applied Engineering, Inje UniversityUU0001067  ); Kim, Chong-Rak   (Department of Biomedical Laboratory Science, Inje UniversityUU0001067  );
  • 초록

    A myofiber of skeletal muscle is composed of myofibrils, sarcolemma (plasma membrane), and constameres, which anchor the myofibrils to the sarcolemma. Achvillin is a recently identified F-actin binding muscle protein, co-isolates with dystrophin and caveolin-3 in low-density sarcolemma of striated muscle, and colocalizes with dystrophin at costameres, the specialized adhesion sites in muscle. Archvillin also binds to nebulin and localizes at myofibrillar Z-discs, the lateral boundaries of the sarcomere in muscle. However other roles of archvillin on the dynamics of myofibrillogenesis remain to be defined. The goal of this study is, by using siRNA-mediated gene silencing technique, to investigate the effect of archvillin on the dynamics of myofibrillogenesis in cell culture of a mouse skeletal myogenic cell line (C2C12), where presumptive myoblasts withdraw from the cell cycle, fuse, undergo de novo myofibrillogenesis, and differentiate into mature myotubes. The roles of archvillin in the assembly and maintenance of myofibril and during the progression of myofibrillogenesis induced in skeletal myoblast following gene silencing in the cell culture were investigated. Fluorescence microscopy demonstrated that the distribution of archvillin was changed along the course of myofibril assembly with nebulin, vinculin and F-actin and then located at Z-lines with nebulin. Fluorescence microscopy demonstrated that knockdown of mouse archvillin expression led to an impaired assembly of new myofibrillar clusters and delayed fusion and myofibrillogenesis although the mouse archvillin siRNA did not affect those expressions of archvillin binding proteins, such as nebulin and F-actin. This result is corresponded with that of RT-PCR and western blots. When the perturbed archvillin was rescued by co-transfection with GFP or Red tagged human archvillin construct, the inhibited cell fusion and myotube formation was recovered. By using siRNA technique, archvillin was found to be involved in early stage of myofibrillogenesis. Therefore, the current data suggest the idea that archvillin plays critical roles on cell fusion and dynamic myofibril assembly.


  • 주제어

    Archvillin .   Myofibril assembly .   Sarcolemma .   Costameres .   Sarcomere .   C2C12 .   siRNA.  

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