Premium
Nature of “Tau” immunoreactivity in normal myonuclei and inclusion body myositis
Author(s) -
Salajegheh Mohammad,
Pinkus Jack L.,
Nazareno Remedios,
Amato Anthony A.,
Parker Kenneth C.,
Greenberg Steven A.
Publication year - 2009
Publication title -
muscle and nerve
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.025
H-Index - 145
eISSN - 1097-4598
pISSN - 0148-639X
DOI - 10.1002/mus.21471
Subject(s) - inclusion body myositis , sarcoplasm , myositis , antibody , inclusion bodies , laser capture microdissection , immunohistochemistry , myopathy , biology , microbiology and biotechnology , pathology , chemistry , endoplasmic reticulum , biochemistry , anatomy , medicine , immunology , gene expression , escherichia coli , gene
Sarcoplasmic accumulation of phosphorylated‐tau has been widely stated to occur in and contribute to the pathogenesis of muscle disease in inclusion body myositis. Twenty inflammatory myopathy and 10 normal muscle samples along with a range of other tissues were stained with anti‐“tau” antibodies (tau‐5, pS422, and SMI‐31). Myonuclear and sarcoplasmic fractions were prepared using differential solubilization and laser‐capture microdissection, and immunoblots were performed using pS422 and SMI‐31 antibodies. All three antibodies demonstrated anti‐tau immunoreactivity in myonuclei from normal and diseased muscle, but not in nuclei from other tissues. Western blots showed pS422 and SMI‐31 immunoreactivity against nuclear proteins outside the region expected for phosphorylated‐tau. Antibodies previously reported to indicate abnormal accumulation of phosphorylated‐tau in IBM myofibers react to normal myonuclei and recognize proteins other than tau. Normal myonuclei contain neurofilament H or other unidentified 200 kDa proteins with similar phosphorylated motifs accounting for SMI‐31 immunoreactivity. Muscle Nerve, 2009