Univ Paris-Est Créteil, INSERM, U955 IMRB, F-94010, Créteil, France.
École nationale vétérinaire d'Alfort, U955 IMRB, F-94700, Maisons-Alfort, France.
EMBO Rep. 2024 Nov;25(11):4898-4920. doi: 10.1038/s44319-024-00249-9. Epub 2024 Oct 2.
Becker muscular dystrophy (BMD) is an X-linked disorder due to in-frame mutations in the DMD gene, leading to a less abundant and truncated dystrophin. BMD is less common and severe than Duchenne muscular dystrophy (DMD) as well as less investigated. To accelerate the search for innovative treatments, we developed a rat model of BMD by deleting the exons 45-47 of the Dmd gene. Here, we report a functional and histopathological evaluation of these rats during their first year of life, compared to DMD and control littermates. BMD rats exhibit moderate damage to locomotor and diaphragmatic muscles but suffer from a progressive cardiomyopathy. Single nuclei RNA-seq analysis of cardiac samples revealed shared transcriptomic abnormalities in BMD and DMD rats and highlighted an altered end-addressing of TMEM65 and Connexin-43 at the intercalated disc, along with electrocardiographic abnormalities. Our study documents the natural history of a translational preclinical model of BMD and reports a cellular mechanism for the cardiac dysfunction in BMD and DMD offering opportunities to further investigate the organization role of dystrophin in intercellular communication.
贝克肌营养不良症(BMD)是一种 X 连锁疾病,由于 DMD 基因突变导致肌营养不良蛋白含量减少和截断。BMD 比杜氏肌营养不良症(DMD)少见且严重,研究也较少。为了加速寻找创新治疗方法,我们通过删除 Dmd 基因的外显子 45-47 ,建立了 BMD 大鼠模型。在这里,我们报告了这些大鼠在其生命的第一年中的功能和组织病理学评估,与 DMD 和对照组同窝仔鼠进行比较。BMD 大鼠表现出运动和膈肌肌肉的中度损伤,但患有进行性心肌病。心脏样本的单细胞 RNA-seq 分析显示 BMD 和 DMD 大鼠存在共享的转录组异常,并突出了在闰盘处 TMEM65 和连接蛋白 43 的末端寻址改变,以及心电图异常。我们的研究记录了 BMD 转化前临床模型的自然病史,并报告了 BMD 和 DMD 心脏功能障碍的细胞机制,为进一步研究肌营养不良蛋白在细胞间通讯中的组织作用提供了机会。