Histopathological Characterization of the Skeletal Myopathy in rasH2 Mice Carrying Human Prototype c-Ha-ras Gene

Journal of Veterinary Medical Science

Takayuki TSUCHIYA¹  Shirou TAKAGI¹  Tetsuya SAKAIRI¹  Fumiko SANO¹  Jiro SUGIMOTO¹  Miyoko OKADA¹ 

[1] Toxicology Laboratory, Pharmaceuticals Research Center, Mitsubishi Pharma Corporation

关键词: histopathology;    rasH2 mouse;    skeletal myopathy;   

DOI  :  10.1292/jvms.67.481

学科分类：兽医学

来源: Japanese Society of Veterinary Science

【 摘 要 】

References(43)Cited-By(1)A skeletal myopathy is found in approximately 100% of rasH2 mice. To confirm detailed features of the rasH2 skeletal myopathy, the biceps femoris, diaphragm, triceps brachii, gastrocnemial (types I and II fiber-mixed muscles) and soleus muscle (type I fiber-dominant muscle) obtained from male rasH2 and non-transgenic littermates aged 10-13 and 34 weeks were examined. Variations in the muscle fiber size, early-scattered degeneration/necrosis and regeneration of muscle fibers were detected in 10-13-week-old rasH2 mice. The severity of the above muscular lesions was more prominent in older rasH2 mice. These lesions were noted in the type II myofiber dominant muscles (biceps femoris, triceps brachii and gastrocnemial). NADH-TR stain clearly demonstrated a disorganized intermyofibrillar network and necrotic change in muscle fibers. No specific morphological changes, like rod structure or tubular aggregation seen in some types of myopathy, were noted in Gomori trichrome and NADH-TR stains in the rasH2 mouse like in many types of muscular dystrophy. Electronmicroscopically, occasional muscle fiber degeneration/regeneration, invaded phagocytic cells, indistinct Z-band suggesting excessive contraction and dilatation of the sarcoplasmic reticulum were observed. In summary, the skeletal myopathy occurring in rasH2 mice is consistent with muscular dystrophy characterized morphologically by progressive degeneration and regeneration of myofibers. The myopathy is confined to the type II myofiber predominant muscles and is not associated with any pathognomonic lesions. These characteristics will provide us with a useful model for research in muscular dystrophy of diverse myofibers.

【 授权许可】

Unknown