Rader Erik P, Layner Kayla N, Triscuit Alyssa M, Kashon Michael L, Gu Ja K, Ensey James, Baker Brent A
Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, Morgantown, WV 26505, United States.
Exp Gerontol. 2015 Dec;72:138-49. doi: 10.1016/j.exger.2015.09.020. Epub 2015 Oct 8.
Recovery from contraction-induced injury is impaired with aging. At a young age, the secondary response several days following contraction-induced injury consists of edema, inflammatory cell infiltration, and segmental muscle fiber degeneration to aid in the clearance of damaged tissue and repair. This morphological response has not been wholly established at advanced age. Our aim was to characterize muscle fiber morphology 3 and 10 days following stretch-shortening contractions (SSCs) varying in repetition number (i.e. 0, 30, 80, and 150) for young and old rats. For muscles of young rats, muscle fiber degeneration was overt at 3 days exclusively after 80 or 150 SSCs and returned significantly closer to control values by 10 days. For muscles of old rats, no such responses were observed. Transcriptional microarray analysis at 3 days demonstrated that muscles of young rats differentially expressed up to 2144 genes while muscles of old rats differentially expressed 47 genes. Bioinformatic analysis indicated that cellular movement was a major biological process over-represented with genes that were significantly altered by SSCs especially for young rats. Protein levels in muscle for various cytokines and chemokines, key inflammatory factors for cell movement, increased 3- to 50-fold following high-repetition SSCs for young rats with no change for old rats. This age-related differential response was insightful given that for control (i.e. 0 SSCs) conditions, protein levels of circulatory cytokines/chemokines were increased with age. The results demonstrate ongoing systemic low-grade inflammatory signaling and subsequent desensitization of the cytokine/chemokine and morphological response to contraction-induced injury with aging - features which accompany age-related impairment in muscle recovery.
收缩诱导损伤后的恢复能力会随着年龄增长而受损。在年轻时,收缩诱导损伤后数天的二次反应包括水肿、炎性细胞浸润和节段性肌纤维变性,以帮助清除受损组织并进行修复。这种形态学反应在老年时尚未完全形成。我们的目的是对年轻和老年大鼠在不同重复次数(即0、30、80和150次)的伸缩收缩(SSC)后3天和10天的肌纤维形态进行表征。对于年轻大鼠的肌肉,仅在80次或150次SSC后3天出现明显的肌纤维变性,到10天时显著恢复至更接近对照值。对于老年大鼠的肌肉,未观察到此类反应。3天时的转录微阵列分析表明,年轻大鼠的肌肉差异表达多达2144个基因,而老年大鼠的肌肉差异表达47个基因。生物信息学分析表明,细胞运动是一个主要的生物学过程,在SSC显著改变的基因中过度表达,尤其是对于年轻大鼠。年轻大鼠在高重复次数SSC后,肌肉中各种细胞因子和趋化因子(细胞运动的关键炎症因子)的蛋白质水平增加了3至50倍,而老年大鼠则无变化。鉴于在对照(即0次SSC)条件下,循环细胞因子/趋化因子的蛋白质水平随年龄增加,这种与年龄相关的差异反应很有启发性。结果表明,随着年龄增长,存在持续的全身性低度炎症信号,以及随后细胞因子/趋化因子和对收缩诱导损伤的形态学反应的脱敏,这些特征伴随着与年龄相关的肌肉恢复受损。