De Biase Davide, Piegari Giuseppe, Prisco Francesco, Cimmino Ilaria, d'Aquino Ilaria, Baldassarre Valeria, Oriente Francesco, Papparella Serenella, Paciello Orlando
Department of Veterinary Medicine and Animal Production, Unit of Pathology, University of Naples "Federico II", 80137 Naples, Italy.
Department of Translational Medicine, University of Naples "Federico II", 80131 Naples, Italy.
Int J Mol Sci. 2021 Mar 30;22(7):3609. doi: 10.3390/ijms22073609.
Sarcopenia is defined as the age-related loss of skeletal muscle mass, quality, and strength. The pathophysiological mechanisms underlying sarcopenia are still not completely understood. The aim of this work was to evaluate, for the first time, the expression of NLRP3 inflammasome in bovine skeletal muscle in order to investigate the hypothesis that inflammasome activation may trigger and sustain a pro-inflammatory environment leading to sarcopenia. Samples of skeletal muscle were collected from 60 cattle belonging to three age-based groups. Morphologic, immunohistochemical and molecular analysis were performed to assess the presence of age-related pathologic changes and chronic inflammation, the expression of NLRP3 inflammasome and to determine the levels of interleukin-1β, interleukin-18 and tumor necrosis factor alpha in muscle tissue. Our results revealed the presence of morphologic sarcopenia hallmark, chronic lymphocytic inflammation and a type II fibers-selective NLRP3 expression associated to a significant decreased number of immunolabeled-fibers in aged animals. Moreover, we found a statistically significant age-related increase of pro-inflammatory cytokines such as interleukin-1β and interleukin-18 suggesting the activation of NLRP3 inflammasome. Taken together, our data suggest that NLRP3 inflammasome components may be normally expressed in skeletal muscle, but its priming and activation during aging may contribute to enhance a pro-inflammatory environment altering normal muscular anabolism and metabolism.
肌肉减少症被定义为与年龄相关的骨骼肌质量、质量和力量的丧失。肌肉减少症背后的病理生理机制仍未完全了解。这项工作的目的是首次评估NLRP3炎性小体在牛骨骼肌中的表达,以研究炎性小体激活可能引发并维持促炎环境导致肌肉减少症的假设。从属于三个基于年龄组的60头牛身上采集骨骼肌样本。进行形态学、免疫组织化学和分子分析,以评估与年龄相关的病理变化和慢性炎症的存在、NLRP3炎性小体的表达,并确定肌肉组织中白细胞介素-1β、白细胞介素-18和肿瘤坏死因子α的水平。我们的结果显示,在老年动物中存在形态学上的肌肉减少症标志、慢性淋巴细胞炎症以及与免疫标记纤维数量显著减少相关的II型纤维选择性NLRP3表达。此外,我们发现促炎细胞因子如白细胞介素-1β和白细胞介素-18在统计学上与年龄相关的显著增加,表明NLRP3炎性小体被激活。综上所述,我们的数据表明,NLRP3炎性小体成分可能在骨骼肌中正常表达,但其在衰老过程中的启动和激活可能有助于增强促炎环境,改变正常的肌肉合成代谢和代谢。