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1.
Clin Case Rep ; 10(11): e6569, 2022 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-36381059

RESUMO

Refractory dysphasia could be the main symptom of Antisynthetase syndrome (ASS). IVIG may have a major impact in the successful treatment of dysphasia in patients with ASS. In our patient with ASS, IVIG treatment was an unreplaceable treatment option, and the patient regains her ability to swallow within 2 days.

2.
J Muscle Res Cell Motil ; 34(5-6): 349-56, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23748997

RESUMO

Abnormal intracellular Ca(2+) handling is an important factor in the progressive functional decline of dystrophic muscle. In the present study, we investigated the function of sarco(endo)plasmic reticulum (SR) Ca(2+) ATPase (SERCA) in various dystrophic muscles of mouse models of Duchenne muscular dystrophy. Our studies show that the protein expression of sarcolipin, a key regulator of the SERCA pump is abnormally high and correlates with decreased maximum velocity of SR Ca(2+) uptake in the soleus, diaphragm and quadriceps of mild (mdx) and severe (mdx:utr-/-) dystrophic mice. These changes are more pronounced in the muscles of mdx:utr-/- mice. We also found increased expression of SERCA2a and calsequestrin specifically in the dystrophic quadriceps. Immunostaining analysis further showed that SERCA2a expression is associated both with fibers expressing slow-type myosin and regenerating fibers expressing embryonic myosin. Together, our data suggest that sarcolipin upregulation is a common secondary alteration in all dystrophic muscles and contributes to the abnormal elevation of intracellular Ca(2+) concentration via SERCA inhibition.


Assuntos
Cálcio/metabolismo , Retículo Endoplasmático/metabolismo , Proteínas Musculares/biossíntese , Músculo Esquelético/metabolismo , Distrofia Muscular de Duchenne/metabolismo , Proteolipídeos/biossíntese , Animais , Modelos Animais de Doenças , Camundongos , Camundongos Endogâmicos C57BL , Músculo Esquelético/citologia , ATPases Transportadoras de Cálcio do Retículo Sarcoplasmático/metabolismo
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