Dirks Amie J, Leeuwenburgh Christiaan
Biochemistry of Aging Laboratory, University of Florida, Gainesville, FL 32611, USA.
Free Radic Biol Med. 2004 Jan 1;36(1):27-39. doi: 10.1016/j.freeradbiomed.2003.10.003.
The mechanisms of apoptosis in the loss of myocytes in skeletal muscle with age and the role of mitochondrial and sarcoplasmic reticulum-mediated pathways of apoptosis are unknown. Moreover, it is unknown whether lifelong calorie restriction prevents apoptosis in skeletal muscle and reverses age-related alterations in apoptosis signaling. We investigated key apoptotic regulatory proteins in the gastrocnemius muscle of 12 and 26 month old ad libitum fed and 26 month old calorie-restricted male Fischer-344 rats. We found that apoptosis increased with age and that calorie-restricted rats showed less apoptosis compared with their age-matched cohorts. Moreover, pro- and cleaved caspase-3 levels increased significantly with age and calorie-restricted rats had significantly lower levels than the aged ad libitum group. Neither age nor calorie restriction had any effect on muscle caspase-3 enzyme activity, but the levels of X-linked inhibitor of apoptosis, particularly an inhibitor of caspase-3, increased with age and were reduced significantly in the 26 month old calorie-restricted cohort. The apoptotic inhibitor apoptosis repressor with a caspase recruitment domain (ARC), which inhibits cytochrome c release, underwent an age-associated decline in the cytosol but increased with calorie restriction. In contrast, mitochondrial ARC levels increased with age and were lower in calorie-restricted rats than in age-matched controls, suggesting a translocation of this protein to attenuate oxidative stress. The translocation of ARC may explain the reduction in cytosolic cytochrome c levels observed with age and calorie restriction. Moreover, we found a striking approximately 350% increase in the expression of procaspase-12 (caspase located at the sarcoplasmic reticulum) with age which was significantly lower in the 26 month old calorie-restricted group. The total protein level of apoptosis-inducing factor in the plantaris muscle increased with age and was reduced calorie-restricted rats compared with age-matched controls, but there were no significant changes in this pro-apoptotic protein in the isolated nuclei. Calorie restriction is able to lower the apoptotic potential in aged skeletal muscle by altering several key apoptotic proteins toward cellular survival, thereby reducing the potential for sarcopenia.
随着年龄增长,骨骼肌中肌细胞丧失过程中凋亡的机制以及线粒体和肌浆网介导的凋亡途径的作用尚不清楚。此外,终身热量限制是否能预防骨骼肌凋亡并逆转与年龄相关的凋亡信号改变也不清楚。我们研究了12个月和26个月大的自由摄食雄性Fischer-344大鼠以及26个月大的热量限制雄性Fischer-344大鼠腓肠肌中的关键凋亡调节蛋白。我们发现,凋亡随年龄增加,与年龄匹配的对照组相比,热量限制大鼠的凋亡较少。此外,前半胱天冬酶-3和裂解的半胱天冬酶-3水平随年龄显著增加,热量限制大鼠的水平明显低于老年自由摄食组。年龄和热量限制对肌肉半胱天冬酶-3酶活性均无影响,但X连锁凋亡抑制蛋白,尤其是半胱天冬酶-3的一种抑制剂,其水平随年龄增加,在26个月大的热量限制组中显著降低。具有半胱天冬酶募集结构域的凋亡抑制蛋白(ARC)可抑制细胞色素c释放,其在胞浆中的水平随年龄下降,但随热量限制而增加。相反,线粒体ARC水平随年龄增加,热量限制大鼠的线粒体ARC水平低于年龄匹配的对照组,提示该蛋白发生易位以减轻氧化应激。ARC的易位可能解释了随年龄和热量限制观察到的胞浆细胞色素c水平降低。此外,我们发现前半胱天冬酶-12(位于肌浆网的半胱天冬酶)的表达随年龄显著增加约350%,在26个月大的热量限制组中显著降低。与年龄匹配的对照组相比,比目鱼肌中凋亡诱导因子的总蛋白水平随年龄增加,热量限制大鼠的水平降低,但在分离的细胞核中,这种促凋亡蛋白没有显著变化。热量限制能够通过改变几种关键的凋亡蛋白使其向细胞存活方向发展,从而降低老年骨骼肌的凋亡潜能,进而减少肌肉减少症的发生可能性。