Machida Shuichi, Booth Frank W
Department of Biomedical Sciences, University of Missouri-Columbia, E102 Veterinary Medical Building, 1600 East Rollins Road, Columbia, MO 65211, USA.
Exp Gerontol. 2004 Oct;39(10):1521-5. doi: 10.1016/j.exger.2004.08.009.
Evidence implies that satellite cells could play some limiting role in aged muscle undergoing repair or maintenance of mass, which is of potential clinical concern as this could contribute to sarcopenia. Further, insufficient information is available concerning the cellular mechanisms responsible for the lower rat satellite cell proliferation in old animals. Thus, it was hypothesized that the following proteins would be increased in nuclei of satellite cells from old rat skeletal muscle: the cyclin-dependent kinase (CDK) inhibitors p21(WAF1/CIP1) and p27(Kip1) as well as the transcription factors p53 and Forkhead box, subgroup O1 (FOXO1). In addition, the NAD(+)-dependent histone deacetylase SIRT1, the mammalian ortholog of the yeast SIR2 (silence information regulator 2) and a member of the Sirtuin family, was hypothesized to decrease in satellite cell nuclei of old rats. Old satellite cells (30-months old) exhibited a lesser number of BrdU-positive cells as compared to satellite cells (3-months old) from young growing animals. Western blot analysis demonstrated that nuclei of old satellite cells accumulated the cell cycle inhibitors p21(WAF1/CIP1) and p27(Kip1). In addition, nuclear p53 and FOXO1 proteins were also higher in old satellite cells than in cells from young growing animals. These data indicated both p53/p21(WAF1/CIP1)- and FOXO1/p27(Kip1)-dependent pathways might contribute to the age-associated decrease in satellite cell proliferation. Cytoplasmic manganese superoxide dismutase (MnSOD), a gene driven by FOXO1, was higher in old satellite cells. Unexpectedly, nuclear SIRT1 was also increased in old satellite cells compared with satellite cells from young growing animals. The physiological significance of enhanced nuclear SIRT1 expression in old satellite cells remains elusive at this time. In summary, satellite cells in old rats have nuclear accumulation of proteins inhibiting the cell cycle as compared to young, growing animals.
有证据表明,卫星细胞可能在衰老肌肉的修复或质量维持过程中发挥某种限制作用,这在临床上具有潜在的重要性,因为这可能导致肌肉减少症。此外,关于导致老年动物卫星细胞增殖率较低的细胞机制,目前可用信息不足。因此,研究人员提出假设:老年大鼠骨骼肌卫星细胞核中的以下蛋白质会增加,即细胞周期蛋白依赖性激酶(CDK)抑制剂p21(WAF1/CIP1)和p27(Kip1),以及转录因子p53和叉头框O1亚组(FOXO1)。此外,研究人员还提出假设:老年大鼠卫星细胞核中的NAD(+)依赖性组蛋白脱乙酰酶SIRT1会减少,SIRT1是酵母SIR2(沉默信息调节因子2)的哺乳动物同源物,属于沉默调节蛋白家族。与年轻生长动物的卫星细胞(3个月大)相比,老年卫星细胞(30个月大)的BrdU阳性细胞数量较少。蛋白质印迹分析表明,老年卫星细胞核中积累了细胞周期抑制剂p21(WAF1/CIP1)和p27(Kip1)。此外,老年卫星细胞核中的p53和FOXO1蛋白也比年轻生长动物的细胞中更高。这些数据表明,p53/p21(WAF1/CIP1)和FOXO1/p27(Kip1)依赖性途径可能都导致了卫星细胞增殖随年龄增长而下降。由FOXO1驱动的基因——细胞质锰超氧化物歧化酶(MnSOD),在老年卫星细胞中含量更高。出乎意料的是,与年轻生长动物的卫星细胞相比,老年卫星细胞核中的SIRT1也增加了。目前,老年卫星细胞核中SIRT1表达增强的生理意义仍不清楚。总之,与年轻生长动物相比,老年大鼠的卫星细胞存在抑制细胞周期的蛋白质在细胞核中的积累。