Carrell Ellie M, Coppola Aundrea R, McBride Helen J, Dirksen Robert T
Department of Physiology and Pharmacology, University of Rochester, Rochester, New York, USA; and.
Department of Inflammation Research, Amgen Incorporated, Thousand Oaks, California, USA.
FASEB J. 2016 Dec;30(12):4109-4119. doi: 10.1096/fj.201600621R. Epub 2016 Sep 1.
Orai1 is a transmembrane protein that forms homomeric, calcium-selective channels activated by stromal interaction molecule 1 (STIM1) after depletion of intracellular calcium stores. In adult skeletal muscle, depletion of sarcoplasmic reticulum calcium activates STIM1/Orai1-dependent store-operated calcium entry. Here, we used constitutive and inducible muscle-specific Orai1-knockout (KO) mice to determine the acute and long-term developmental effects of Orai1 ablation on muscle structure and function. Skeletal muscles from constitutive, muscle-specific Orai-KO mice exhibited normal postnatal growth and fiber type differentiation. However, a significant reduction in fiber cross-sectional area occurred by 3 mo of age, with the most profound reduction observed in oxidative, fatigue-resistant fiber types. Soleus muscles of constitutive Orai-KO mice exhibited a reduction in unique type I fibers, concomitant with an increase in hybrid fibers expressing both type I and type IIA myosins. Additionally, ex vivo force measurements showed reduced maximal specific force and in vivo exercise assays revealed reduced endurance in constitutive muscle-specific Orai-KO mice. Using tamoxifen-inducible, muscle-specific Orai-KO mice, these functional deficits were found to be the result of the delayed fiber changes resulting from an early developmental loss of Orai1 and not the result of an acute loss of Orai1-dependent store-operated calcium entry.-Carrell, E. M., Coppola, A. R., McBride, H. J., Dirksen, R. T. Orai1 enhances muscle endurance by promoting fatigue-resistant type I fiber content but not through acute store-operated Ca entry.
Orai1是一种跨膜蛋白,在细胞内钙库耗竭后,它会形成由基质相互作用分子1(STIM1)激活的同聚体钙选择性通道。在成年骨骼肌中,肌浆网钙的耗竭会激活STIM1/Orai1依赖性的钙库操纵性钙内流。在此,我们使用组成型和诱导型肌肉特异性Orai1基因敲除(KO)小鼠来确定Orai1基因敲除对肌肉结构和功能的急性和长期发育影响。组成型肌肉特异性Orai基因敲除小鼠的骨骼肌在出生后生长和纤维类型分化方面表现正常。然而,到3月龄时纤维横截面积显著减小,在氧化型、抗疲劳纤维类型中观察到最明显的减小。组成型Orai基因敲除小鼠的比目鱼肌中独特的I型纤维减少,同时表达I型和IIA型肌球蛋白的混合纤维增加。此外,离体力量测量显示组成型肌肉特异性Orai基因敲除小鼠的最大比力降低,体内运动试验显示其耐力下降。使用他莫昔芬诱导的肌肉特异性Orai基因敲除小鼠,发现这些功能缺陷是由于Orai1早期发育缺失导致的纤维变化延迟所致,而非Orai1依赖性钙库操纵性钙内流急性缺失的结果。-卡雷尔,E.M.,科波拉,A.R.,麦克布赖德,H.J.,德克森,R.T.Orai1通过促进抗疲劳I型纤维含量来增强肌肉耐力,但不是通过急性钙库操纵性钙内流。