骨骼肌中 SERCA1 的过表达可减轻肌肉萎缩并改善 ALS 小鼠模型的运动功能。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-01-01 DOI:10.3233/JND-230123
Davi A G Mázala, Dapeng Chen, Eva R Chin
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引用次数: 0

摘要

背景:肌萎缩性脊髓侧索硬化症(ALS)的特征是肌肉质量和肌肉功能的逐渐丧失。我们实验室之前的研究表明,ALS 小鼠模型的骨骼肌表现出细胞内钙(Ca2 +)水平升高和内质网(ER)应激增强:目的:研究在骨骼肌中过表达肌质网(SR)Ca2 + ATPase 1(SERCA1)是否会改善细胞内 Ca2 + 的处理、减轻 ER 应激并改善 ALS 转基因小鼠的运动功能:B6SJL-Tg(SOD1*G93A)1Gur/J(ALS-Tg)小鼠与骨骼肌α-肌动蛋白SERCA1过表达小鼠杂交,产生野生型(WT)、SERCA1过表达(WT/+SERCA1)、ALS-Tg和SERCA1过表达ALS-Tg(ALS-Tg/+SERCA1)小鼠。每周对小鼠的运动功能(握力测试)进行评估,并在小鼠16周大时采集其骨骼肌,以评估肌肉质量、SR-Ca2 + ATPase活性、SERCA1和ER应激蛋白--蛋白二硫异构酶(PDI)、GRP78/BiP和C/EBP同源蛋白(CHOP)的水平。还从屈指肌分离出单肌纤维,以评估静息和峰值 Fura-2 比率的变化:结果:与 ALS-Tg 相比,ALS-Tg/+SERCA1 小鼠的运动功能得到改善,发病时间推迟,肌肉质量提高。此外,ALS-Tg/+SERCA1 小鼠的 SERCA1 蛋白水平和 SR-Ca2 + ATPase 活性恢复到了 WT 小鼠的水平。意想不到的是,SERCA-1 的过表达增加了 WT 小鼠和 ALS-Tg 小鼠体内 ER 压力制造者 Grp78/BiP 的水平,而 PDI 或 CHOP 的蛋白水平却没有改变。最后,与 ALS-Tg 小鼠相比,ALS-Tg/+SERCA1 的单个肌肉纤维具有相似的静息水平,但峰值 Fura-2 水平(30 Hz 和 100 Hz)较低:这些数据表明,过表达 SERCA1 可减轻 ALS-Tg 小鼠肌肉质量的逐渐丧失并维持运动功能,同时不会降低静息 Ca2 + 水平或 ER 应激。
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SERCA1 Overexpression in Skeletal Muscle Attenuates Muscle Atrophy and Improves Motor Function in a Mouse Model of ALS.

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 α-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 in WT mice. Unexpectedly, SERCA-1 overexpression increased levels of the ER stress maker Grp78/BiP in both WT and 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.

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