Reddy Avula C P, Lawrence Richard A, Zaman Khaliquz, Fernandes Gabriel
University of Texas Health Science Center, Department of Medicine, San Antonio 78229-3900, USA.
J Clin Immunol. 2002 Jul;22(4):206-19. doi: 10.1023/a:1016088708457.
Our earlier studies have shown that calorie restriction and n-3 fatty acids inhibit autoimmune disease and prolong life span. Experiments were designed to study the alteration of apoptosis and its mediators in B/W mice fed either n-6 fatty acids [5% corn oil (CO)] or n-3 fatty acids [5% fish oil (FO)] and either allowed access to the diet ad libitum (AL) or restricted in caloric intake by 40% (CR), from 4 weeks of age. At 4 months (young) and 9 months (old) mice were killed, splenic lymphocytes were isolated, and apoptosis was measured with Annexin V and PI staining. Apoptosis was decreased in splenic lymphocytes from both young and old CR mice compared to their respective AL-fed control groups regardless of fat source. Increasing apoptosis with age was observed in CO/AL, CO/CR, and FO/AL mice which correlated closely with significantly higher cellular peroxides measured by flow cytometry using dichlorofluourescein diacetate (DCFH-DA), whereas in both CO/CR and FO/CR peroxide levels remained low in old mice. Furthermore, CR increased the proliferative response of splenic lymphocytes and decreased the Fas (CD95) and Fas-L protein expression in CD4+ lymphocytes from old mice. Higher levels of Fas and Fas-L expression were observed in old mice compared to young mice. Bcl-2 levels were elevated in both young and old CR groups compared to the respective AL groups. Calorie restriction prevented the loss of CD8 cells in old mice fed both the CO and the FO diet. In summary, CR resulted in decreased apoptosis accompanied by alterations in Fas, Fas-L, and Bcl-2 expression in old mice, increased life span, and delayed onset of kidney disease.
我们早期的研究表明,热量限制和n-3脂肪酸可抑制自身免疫性疾病并延长寿命。本实验旨在研究从4周龄起分别喂食n-6脂肪酸[5%玉米油(CO)]或n-3脂肪酸[5%鱼油(FO)],且随意进食(AL)或热量摄入限制40%(CR)的B/W小鼠中细胞凋亡及其介质的变化。在4个月(年轻)和9个月(年老)时处死小鼠,分离脾淋巴细胞,并用膜联蛋白V和碘化丙啶染色检测细胞凋亡。与各自的AL喂养对照组相比,无论脂肪来源如何,年轻和年老的CR小鼠脾淋巴细胞中的细胞凋亡均减少。在CO/AL、CO/CR和FO/AL小鼠中观察到细胞凋亡随年龄增加,这与使用二氯荧光素二乙酸酯(DCFH-DA)通过流式细胞术测量的细胞过氧化物显著升高密切相关,而在CO/CR和FO/CR老年小鼠中过氧化物水平均保持较低。此外,CR增加了脾淋巴细胞的增殖反应,并降低了老年小鼠CD4+淋巴细胞中Fas(CD95)和Fas-L蛋白的表达。与年轻小鼠相比,老年小鼠中Fas和Fas-L表达水平更高。与各自的AL组相比,年轻和年老的CR组中Bcl-2水平均升高。热量限制可防止喂食CO和FO饮食的老年小鼠中CD8细胞的丢失。总之,CR导致老年小鼠细胞凋亡减少,同时Fas、Fas-L和Bcl-2表达发生改变,延长了寿命,并延迟了肾病的发病。