SERCA1 Overexpression in Skeletal Muscle Attenuates Muscle Atrophy and Improves Motor Function in a Mouse Model of ALS

被引:3
作者
Mazala, Davi A. G. [1 ,2 ,3 ]
Chen, Dapeng [1 ,4 ]
Chin, Eva R. [1 ,5 ]
机构
[1] Univ Maryland, Sch Publ Hlth, Dept Kinesiol, College Pk, MD USA
[2] Towson Univ, Coll Hlth Profess, Dept Kinesiol, Towson, MD USA
[3] Natl Childrens Hosp, Childrens Natl Res Inst, Ctr Genet Med Res, Washington, DC USA
[4] Zeteo Tech Inc, Sykesville, MD USA
[5] Solve FSHD, Vancouver, BC, Canada
关键词
Amyotrophic lateral sclerosis; SOD1; calcium; SERCA1; ER stress; AMYOTROPHIC-LATERAL-SCLEROSIS; NEURON DEGENERATION; CYSTEINE RESIDUES; EXPRESSION; INACTIVATION; CONTRACTION; RETICULUM; OXIDATION; DAMAGE; ROLES;
D O I
10.3233/JND-230123
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Amyotrophic lateral sclerosis (ALS) is characterized by progressive loss of muscle mass and muscle function. Previous work from our lab demonstrated that skeletal muscles from a mouse model of ALS show elevated intracellular calcium (Ca2+) levels and heightened endoplasmic reticulum (ER) stress. Objective: To investigate whether overexpression of sarcoplasmic reticulum (SR) Ca2+ ATPase 1 (SERCA1) in skeletal muscle would improve intracellular Ca2+ handling, attenuate ER stress, and improve motor function ALS transgenic mice. Methods: B6SJL-Tg (SOD1*G93A)1Gur/J (ALS-Tg) mice were bred with skeletal muscle alpha-actinin SERCA1 overexpressing mice to generate wild type (WT), SERCA1 overexpression (WT/+SERCA1), ALS-Tg, and SERCA1 overexpressing ALS-Tg (ALS-Tg/+SERCA1) mice. Motor function (grip test) was assessed weekly and skeletal muscles were harvested at 16 weeks of age to evaluate muscle mass, SR-Ca2+ ATPase activity, levels of SERCA1 and ER stress proteins - protein disulfide isomerase (PDI), Grp78/BiP, and C/EBP homologous protein (CHOP). Single muscle fibers were also isolated from the flexor digitorum brevis muscle to assess changes in resting and peak Fura-2 ratios. Results: ALS-Tg/+SERCA1 mice showed improved motor function, delayed onset of disease, and improved muscle mass compared to ALS-Tg. Further, ALS-Tg/+SERCA1 mice returned levels of SERCA1 protein and SR-Ca2+ ATPase activity back to levels inWTmice. Unexpectedly, SERCA-1 overexpression increased levels of the ER stress maker Grp78/BiP in both WTand ALS-Tg mice, while not altering protein levels of PDI or CHOP. Lastly, single muscle fibers from ALS-Tg/+SERCA1 had similar resting but lower peak Fura-2 levels (at 30 Hz and 100 Hz) compared to ALS-Tg mice. Conclusions: These data indicate that SERCA1 overexpression attenuates the progressive loss of muscle mass and maintains motor function in ALS-Tg mice while not lowering resting Ca2+ levels or ER stress.
引用
收藏
页码:315 / 326
页数:12
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