Beta2-Adrenergic Stimulation Induces Resistance Training-Like Adaptations in Human Skeletal Muscle: Potential Role of KLHL41.

IF 3.5 2区 医学 Q1 SPORT SCIENCES Scandinavian Journal of Medicine & Science in Sports Pub Date : 2024-10-01 DOI:10.1111/sms.14736
Søren Jessen, Júlia Prats Quesada, Andrea Di Credico, Roger Moreno-Justicia, Richard Wilson, Glenn Jacobson, Jens Bangsbo, Atul S Deshmukh, Morten Hostrup
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Abstract

Skeletal muscle mass plays a pivotal role in metabolic function, but conditions such as bed rest or injury often render resistance training impractical. The beta2-adrenergic receptor has been highlighted as a potential target to promote muscle hypertrophy and treat atrophic conditions. Here, we investigate the proteomic changes associated with beta2-adrenergic-mediated muscle hypertrophy, using resistance training as a hypertrophic comparator. We utilize MS-based proteomics to map skeletal muscle proteome remodeling in response to beta2-adrenergic stimulation or resistance training as well as cell model validation. We report that beta2-adrenergic stimulation mimics multiple features of resistance training in proteome-wide remodeling, comprising systematic upregulation of ribosomal subunits and concomitant downregulation of mitochondrial proteins. Approximately 20% of proteins were regulated in both conditions, comprising proteins involved in steroid metabolism (AKR1C1, AKR1C2, AKRC1C3), protein-folding (SERPINB1), and extracellular matrix organization (COL1A1, COL1A2). Among overall most significantly upregulated proteins were kelch-like family members (KLHL) 40 and 41. In follow-up experiments, we identify KLHL41 as having novel implications for beta2-adrenergic-mediated muscle hypertrophy. Treating C2C12 cells with beta2-agonist for 96 h increased myotube diameter by 48% (p < 0.001). This anabolic effect was abolished by prior knockdown of KLHL41. Using siRNA, KLHL41 abundance was decreased by 60%, and the anabolic response to beta2-agonist was diminished (+ 15%, i.e., greater in the presence of KLHL41, knock-down × treatment: p = 0.004). In conclusion, protein-wide remodeling induced by beta2-adrenergic stimulation mimics multiple features of resistance training, and thus the beta2-adrenergic receptor may be a target with therapeutic potential in the treatment of muscle wasting conditions without imposing mechanical load.

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β2-肾上腺素能刺激诱导人类骨骼肌产生类似阻力训练的适应性:KLHL41 的潜在作用。
骨骼肌质量在新陈代谢功能中起着举足轻重的作用,但卧床休息或受伤等情况往往使阻力训练变得不切实际。β2-肾上腺素能受体被认为是促进肌肉肥大和治疗萎缩性疾病的潜在靶点。在这里,我们以阻力训练作为肥大的比较对象,研究了与β2-肾上腺素能介导的肌肉肥大相关的蛋白质组变化。我们利用质谱蛋白质组学绘制了β2-肾上腺素能刺激或阻力训练时骨骼肌蛋白质组重塑的图谱,并进行了细胞模型验证。我们报告说,β2-肾上腺素能刺激在整个蛋白质组的重塑中模拟了阻力训练的多个特征,包括核糖体亚基的系统性上调和线粒体蛋白质的同步下调。约有 20% 的蛋白质在两种情况下都受到了调节,其中包括参与类固醇代谢(AKR1C1、AKR1C2、AKRC1C3)、蛋白质折叠(SERPINB1)和细胞外基质组织(COL1A1、COL1A2)的蛋白质。在所有上调最明显的蛋白质中,有 Kelch 样家族成员(KLHL)40 和 41。在后续实验中,我们发现 KLHL41 对β2-肾上腺素能介导的肌肉肥大有新的影响。用β2-激动剂处理C2C12细胞96小时后,肌管直径增加了48%(P 2-激动剂的作用减弱(+ 15%,即在KLHL41存在的情况下作用更大,基因敲除×处理:P = 0.004))。总之,β2-肾上腺素能刺激诱导的全蛋白质重塑模拟了阻力训练的多种特征,因此,β2-肾上腺素能受体可能是治疗肌肉萎缩症的一个具有治疗潜力的靶点,而无需施加机械负荷。
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来源期刊
CiteScore
7.90
自引率
4.90%
发文量
162
审稿时长
3 months
期刊介绍: The Scandinavian Journal of Medicine & Science in Sports is a multidisciplinary journal published 12 times per year under the auspices of the Scandinavian Foundation of Medicine and Science in Sports. It aims to publish high quality and impactful articles in the fields of orthopaedics, rehabilitation and sports medicine, exercise physiology and biochemistry, biomechanics and motor control, health and disease relating to sport, exercise and physical activity, as well as on the social and behavioural aspects of sport and exercise.
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