Zhu Wenyuan G, Thomas Aaron C Q, Wilson Gary M, McGlory Chris, Hibbert Jamie E, Flynn Corey Gk, Sayed Ramy K A, Paez Hector G, Meinhold Marius, Jorgenson Kent W, You Jae-Sung, Steinert Nathaniel D, Lin Kuan-Hung, MacInnis Martin J, Coon Joshua J, Phillips Stuart M, Hornberger Troy A
Department of Comparative Biosciences, University of Wisconsin-Madison, Madison, WI, USA.
School of Veterinary Medicine, University of Wisconsin-Madison, Madison, WI, USA.
Nat Metab. 2025 May 15. doi: 10.1038/s42255-025-01298-7.
Endurance and resistance exercise lead to distinct functional adaptations: the former increases aerobic capacity and the latter increases muscle mass. However, the signalling pathways that drive these adaptations are not well understood. Here we identify phosphorylation events that are differentially regulated by endurance and resistance exercise. Using a model of unilateral exercise in male participants and deep phosphoproteomic analyses, we find that a prolonged activation of a signalling pathway involving MKK3b/6, p38, MK2 and mTORC1 occurs specifically in response to resistance exercise. Follow-up studies in both male and female participants reveal that the resistance-exercise-induced activation of MKK3b is highly correlated with the induction of protein synthesis (R = 0.87). Additionally, we show that in mice, genetic activation of MKK3b is sufficient to induce signalling through p38, MK2 and mTORC1, along with an increase in protein synthesis and muscle fibre size. Overall, we identify core components of a signalling pathway that drives the growth-promoting effects of resistance exercise.
前者提高有氧能力,后者增加肌肉质量。然而,驱动这些适应性变化的信号通路尚未完全明确。在此,我们确定了受耐力训练和抗阻训练差异调节的磷酸化事件。通过对男性参与者进行单侧运动模型和深度磷酸化蛋白质组分析,我们发现涉及MKK3b/6、p38、MK2和mTORC1的信号通路的长期激活特异性地发生于抗阻训练后。在男性和女性参与者中开展的后续研究表明,抗阻训练诱导的MKK3b激活与蛋白质合成的诱导高度相关(R = 0.87)。此外,我们还表明,在小鼠中,MKK3b的基因激活足以诱导通过p38、MK2和mTORC1的信号传导,同时增加蛋白质合成和肌肉纤维大小。总体而言,我们确定了一条驱动抗阻训练促进生长作用的信号通路的核心组成部分。