University of Massachusetts Amherst.
University of Connecticut School of Medicine, Farmington.
J Gerontol A Biol Sci Med Sci. 2020 Nov 13;75(12):2333-2341. doi: 10.1093/gerona/glaa136.
Skeletal muscle myopathies represent a common non-pulmonary manifestation of influenza infection, leading to reduced physical function and hospitalization in older adults. However, underlying mechanisms remain poorly understood. Our study examined the effects of influenza virus A pulmonary infection on contractile function at the cellular (single fiber) and molecular (myosin-actin interactions and myofilament properties) levels in soleus and extensor digitorum longus muscles of aged (20 months) C57BL/6 male mice that were healthy or flu-infected for 7 (7-days post-infection; 7-DPI) or 12 days (12-DPI). Cross-sectional area (CSA) of myosin heavy chain (MHC) IIA and IIB fibers was reduced at 12-DPI relative to 7-DPI and healthy. Maximal isometric force in MHC IIA fibers was also reduced at 12-DPI relative to 7-DPI and healthy, resulting in no change in specific force (maximal isometric force divided by CSA). In contrast, MHC IIB fibers produced greater isometric force and specific force at 7-DPI compared to 12-DPI or healthy. The increased specific force in MHC IIB fibers was likely due to greater myofilament lattice stiffness and/or an increased number or stiffness of strongly bound myosin-actin cross-bridges. At the molecular level, cross-bridge kinetics were slower in MHC IIA fibers with infection, while changes in MHC IIB fibers were largely absent. In both fiber types, greater myofilament lattice stiffness was positively related to specific force. This study provides novel evidence that cellular and molecular contractile function is impacted by influenza infection in a fiber type-specific manner, suggesting potential molecular mechanisms to help explain the impact of flu-induced myopathies.
骨骼肌肌病是流感感染的一种常见非肺部表现,可导致老年人身体机能下降和住院治疗。然而,其潜在机制仍知之甚少。本研究检测了流感病毒 A 肺部感染对老龄(20 月龄)C57BL/6 雄性小鼠比目鱼肌和趾长伸肌细胞(单纤维)和分子(肌球蛋白-肌动蛋白相互作用和肌丝特性)水平收缩功能的影响,这些小鼠在健康或流感感染 7(感染后 7 天;7-DPI)或 12 天(12-DPI)时。与 7-DPI 和健康相比,12-DPI 时 MHC IIA 和 IIB 纤维的肌球蛋白重链(MHC)的横截面积(CSA)减少。与 7-DPI 和健康相比,MHC IIA 纤维的最大等长力量也在 12-DPI 时降低,导致比力(最大等长力量除以 CSA)没有变化。相比之下,与 12-DPI 或健康相比,MHC IIB 纤维在 7-DPI 时产生更大的等长力量和比力。MHC IIB 纤维中增加的比力可能是由于肌丝晶格硬度增加和/或牢固结合的肌球蛋白-肌动蛋白横桥数量或硬度增加所致。在分子水平上,感染后 MHC IIA 纤维的横桥动力学更慢,而 MHC IIB 纤维的变化则基本不存在。在这两种纤维类型中,更大的肌丝晶格硬度与比力呈正相关。本研究提供了新的证据,表明流感感染以纤维类型特异性的方式影响细胞和分子收缩功能,这表明了潜在的分子机制,有助于解释流感引起的肌病的影响。