Hsu Ming-Fen, Yu Szu-Hsien, Chuang Sheng-Ju, Kuo Tom Kwang-Chun, Singal Pawan K, Huang Chih-Yang, Kao Chung-Lan, Kuo Chia-Hua
Laboratory of Exercise Biochemistry, University of Taipei, Taipei, Taiwan.
Université Catholique de Louvain and de Duve Institute, Brussels, Belgium.
Aging (Albany NY). 2018 Oct 24;10(10):2900-2910. doi: 10.18632/aging.101595.
Recent findings regarding uses of adipose-derived mesenchymal stem cell (MSC)-lysate on weight loss and improved glucose tolerance in mice on a high-fat diet suggest an encouraging possibility of using MSC lysate for an anti-aging intervention in humans. However, weight loss and lipopenia during late life can be as life-threatening as hyperglycemia during early adulthood. For this 3-year lifelong experiment, a total of 92 rats were randomized into the vehicle-injected group (F=22; M=24) and the MSC lysate injected group (F=22, M=24). We examined longevity, spontaneous locomotor activity, and body composition in rats maintained on a normal diet and received an intermittent treatment of human adipose-derived MSC lysate (3 times a week, 11 times a month given every second month), starting at 12 months of age until natural death. In substantiating previous knowledge regarding the effects of long-term MSC lysate treatments on fat loss and insulin resistance, the present findings also highlighted a shortened average lifespan, a longer inactive time, and a greater bone loss with a relative increase of lean mass in MSC lysate rats with respect to controls. Conclusion: Our data suggest that MSC lysate treatments stimulate disparity in tissue development and produce a cachexia-like effect to decrease longevity.
近期有关脂肪间充质干细胞(MSC)裂解物对高脂饮食小鼠体重减轻和葡萄糖耐量改善作用的研究结果表明,使用MSC裂解物对人类进行抗衰老干预具有令人鼓舞的可能性。然而,晚年的体重减轻和脂肪减少可能与成年早期的高血糖一样危及生命。在这项为期3年的终身实验中,总共92只大鼠被随机分为注射赋形剂组(雌性=22只;雄性=24只)和注射MSC裂解物组(雌性=22只,雄性=24只)。我们研究了正常饮食的大鼠的寿命、自发运动活动和身体组成,并从12个月大开始直至自然死亡,对其进行了人脂肪来源的MSC裂解物的间歇性治疗(每周3次,每隔一个月每月11次)。在证实先前关于长期MSC裂解物治疗对脂肪减少和胰岛素抵抗影响的知识时,目前的研究结果还突出显示,与对照组相比,接受MSC裂解物治疗的大鼠平均寿命缩短、不活动时间延长、骨质流失增加,而瘦体重相对增加。结论:我们的数据表明,MSC裂解物治疗会刺激组织发育差异,并产生恶病质样效应,从而缩短寿命。
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