دورية
Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNAgene mutation
| العنوان: | Emerin deficiency does not exacerbate cardiomyopathy in a murine model of Emery–Dreifuss muscular dystrophy caused by an LMNAgene mutation |
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| المؤلفون: | Wada, Eiji, Matsumoto, Kohei, Susumu, Nao, Kato, Megumi, Hayashi, Yukiko K. |
| المصدر: | The Journal of Physiological Sciences; December 2023, Vol. 73 Issue: 1 |
| مستخلص: | Emery–Dreifuss muscular dystrophy (EDMD), caused by mutations in genes encoding nuclear envelope proteins, is clinically characterized by muscular dystrophy, early joint contracture, and life-threatening cardiac abnormalities. To elucidate the pathophysiological mechanisms underlying striated muscle involvement in EDMD, we previously established a murine model with mutations in Emdand Lmna(Emd−/−/LmnaH222P/H222P; EH), and reported exacerbated skeletal muscle phenotypes and no notable cardiac phenotypes at 12 weeks of age. We predicted that lack of emerin in LmnaH222P/H222Pmice causes an earlier onset and more pronounced cardiac dysfunction at later stages. In this study, cardiac abnormalities of EDMD mice were compared at 18 and 30 weeks of age. Contrary to our expectations, physiological and histological analyses indicated that emerin deficiency causes no prominent differences of cardiac involvement in LmnaH222P/H222Pmice. These results suggest that emerin does not contribute to cardiomyopathy progression in LmnaH222P/H222Pmice. |
| قاعدة البيانات: | Supplemental Index |
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Full Text Finder | تدمد: | 18806546 18806562 |
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| DOI: | 10.1186/s12576-023-00886-0 |