Dennhag Nils, Kahsay Abraha, Nissen Itzel, Nord Hanna, Chermenina Maria, Liu Jiao, Arner Anders, Liu Jing-Xia, Backman Ludvig J, Remeseiro Silvia, von Hofsten Jonas, Pedrosa Domellöf Fatima
Department of Medical and Translational Biology, Umeå University, Umeå, Sweden.
Department of Clinical Sciences, Ophthalmology, Umeå University, Umeå, Sweden.
Nat Commun. 2024 Mar 2;15(1):1950. doi: 10.1038/s41467-024-46187-x.
In muscular dystrophies, muscle fibers loose integrity and die, causing significant suffering and premature death. Strikingly, the extraocular muscles (EOMs) are spared, functioning well despite the disease progression. Although EOMs have been shown to differ from body musculature, the mechanisms underlying this inherent resistance to muscle dystrophies remain unknown. Here, we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscles in zebrafish via transcriptomic profiling. We show that the LIM-protein Fhl2 is increased in response to the knockout of desmin, plectin and obscurin, cytoskeletal proteins whose knockout causes different muscle dystrophies, and contributes to disease protection of the EOMs. Moreover, we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje, significantly improving their survival. Therefore, Fhl2 is a protective agent and a candidate target gene for therapy of muscular dystrophies.
在肌肉萎缩症中,肌纤维丧失完整性并死亡,导致巨大痛苦和过早死亡。引人注目的是,眼外肌(EOMs)得以幸免,尽管疾病进展,但功能良好。虽然已表明眼外肌与身体肌肉组织不同,但这种对肌肉萎缩症的固有抵抗力背后的机制仍然未知。在这里,我们通过转录组分析证明了斑马鱼眼外肌和躯干肌肉对肌肉萎缩症反应中基因表达的重要差异。我们表明,LIM蛋白Fhl2在结蛋白、网蛋白和 obscurin敲除后增加,这些细胞骨架蛋白的敲除会导致不同的肌肉萎缩症,并且Fhl2有助于眼外肌的疾病保护。此外,我们表明fhl2b的异位表达可以部分挽救斑马鱼杜氏肌营养不良模型sapje中的肌肉表型,显著提高它们的存活率。因此,Fhl2是一种保护剂,也是治疗肌肉萎缩症的候选靶基因。