Cellular pathology of the human heart in Duchenne muscular dystrophy (DMD): lessons learned from in vitro modeling

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Publikace nespadá pod Fakultu sportovních studií, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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SVOBODOVÁ Barbora JELÍNKOVÁ Šárka PEŠL Martin BECKEROVÁ Deborah LACAMPAGNE Alain MELI A. C. ROTREKL Vladimír

Rok publikování 2021
Druh Článek v odborném periodiku
Časopis / Zdroj PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www https://link.springer.com/article/10.1007%2Fs00424-021-02589-0
Doi http://dx.doi.org/10.1007/s00424-021-02589-0
Klíčová slova Cardiomyocyte; Contraction; Duchenne muscular dystrophy; In vitro modeling; Heart failure
Popis Duchenne muscular dystrophy is a genetic disorder where an X-linked mutation in the DMD gene initiates pathogenic development caused by the absence of dystrophin protein. This impacts primarily the evolution of a functional muscle tissue resulting in muscle weakness and later severe disability in young male patients leading to an early death. Patients in the final stage develop dilated cardiomyopathy leading ultimately to cardiac or respiratory failure as the cause of death. This review discusses recent advances in modeling the DMD pathology in vitro. It describes in detail the molecular abnormalities found on the cellular and organoid levels. The in vitro pathology is compared to that found in patients. Likewise, the drawbacks and limitations of current models are discussed.
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