Expression of Myoferlin in Skeletal Muscles of Patients with Dysferlinopathy
Autor: | Hiroko Kojima, Masahiko Inoue, Hiroaki Oniki, Ichizo Nishino, Yoshihiro Wakayama, Seiji Shibuya, Takahiro Jimi, Ikuya Nonaka |
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Rok vydání: | 2006 |
Předmět: |
Dysferlinopathy
Pathology medicine.medical_specialty Biopsy Immunoblotting Muscle Proteins Gene mutation Muscular Dystrophies General Biochemistry Genetics and Molecular Biology Quadriceps Muscle Dysferlin Utrophin medicine Humans Myocyte Fluorescent Antibody Technique Indirect Microscopy Immunoelectron biology Calcium-Binding Proteins Membrane Proteins General Medicine medicine.disease Immunohistochemistry biology.protein Dystrophin Immunostaining Limb-girdle muscular dystrophy |
Zdroj: | The Tohoku Journal of Experimental Medicine. 209:109-116 |
ISSN: | 1349-3329 0040-8727 |
DOI: | 10.1620/tjem.209.109 |
Popis: | Myoferlin is a novel protein of unknown function with high homology to dysferlin, the gene mutations of which cause limb girdle muscular dystrophy type 2B and Miyoshi myopathy. The myoferlin gene seems to be a candidate for the modifier, and because of the high homology to dysferlin myoferlin may work as a compensator for the absence of dysferlin in dysferlinopathy. This hypothesis is based on the observation that utrophin, which has 80% homology with dystrophin, is overexpressing in the dystrophin deficient myofibers. To test this hypothesis, we investigated the myoferlin expression by immunoblot and immunohistochemical analysis in muscles of five patients with dysferlinopathy. For this aim, we generated a myoferlin specific antibody that does not cross react with dysferlin, and performed the immunoblot, immunohistochemical and immunoelectron microscopic studies. Immunohistochemical analysis showed that the antibodies against myoferlin and dysferlin clearly stained the normal human myofiber surface membranes. The electron microscopy of single immunogold labeled samples for myoferlin showed the presence of the molecular signal along the normal muscle cell membrane. Immunoblot analysis showed that the intensity of 230-kDa myoferlin band of dysferlinopathy muscle extracts was similar to that of normal muscle extracts. The immunostaining of dysferlinopathy muscles with anti-myoferlin antibody revealed a weak immunoreactivity along the muscle cell surface. Thus, the compensatory overexpression of myoferlin was not detected in muscles with dysferlinopathy. |
Databáze: | OpenAIRE |
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