Sasaki Tsuyoshi, Yamada Eijiro, Uehara Ryota, Okada Shuichi, Chikuda Hirotaka, Yamada Masanobu
Department of Orthopaedic Surgery, Gunma University Graduate School of Medicine, Maebashi, Japan.
Department of Internal Medicine, Division of Endocrinology and Metabolism, Gunma University Graduate School of Medicine, Maebashi, Japan.
iScience. 2023 Aug 25;26(10):107717. doi: 10.1016/j.isci.2023.107717. eCollection 2023 Oct 20.
Sarcopenia is the progressive loss of muscle mass wherein Fyn regulates STAT3 to decrease autophagy. To elucidate the role of inflammation in Fyn-STAT3-dependent autophagy and sarcopenia, here we aimed to investigate the underlying mechanisms using two mouse models of primary and secondary sarcopenia: (1) tail suspension and (2) sciatic denervation. In wild-type mice, the expression of and increased significantly. The expression and phosphorylation levels of STAT3 were also significantly augmented, while autophagic activity was abolished. To investigate Fyn-dependency, we used tail suspension with Fyn-null mice. In tail-suspended wild-type mice, IL-6 expression was increased; however, it was abolished in Fyn-null mice, which maintained autophagy and the expression and ablation of STAT3 phosphorylation. In conclusion, Fyn was found to be associated with the IL-6-STAT3-autophagy axis in sarcopenia. This finding permits a better understanding of sarcopenia-associated metabolic diseases and the possible development of therapeutic interventions.
肌肉减少症是肌肉质量的渐进性丧失,其中Fyn调节信号转导和转录激活因子3(STAT3)以减少自噬。为了阐明炎症在Fyn-STAT3依赖性自噬和肌肉减少症中的作用,我们在此旨在使用原发性和继发性肌肉减少症的两种小鼠模型来研究其潜在机制:(1)尾部悬吊和(2)坐骨神经去支配。在野生型小鼠中,白细胞介素6(IL-6)和肿瘤坏死因子α(TNF-α)的表达显著增加。STAT3的表达和磷酸化水平也显著增强,而自噬活性被消除。为了研究Fyn依赖性,我们对Fyn基因敲除小鼠进行尾部悬吊。在尾部悬吊的野生型小鼠中,IL-6表达增加;然而,在Fyn基因敲除小鼠中IL-6表达被消除,这些小鼠维持自噬以及STAT3磷酸化的表达和消除。总之,发现Fyn与肌肉减少症中的IL-6-STAT3-自噬轴相关。这一发现有助于更好地理解与肌肉减少症相关的代谢疾病以及治疗干预措施的可能发展。