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Strain-dependent response to stimulation in middle-aged rat macrophages: A quest after a useful indicator of healthy aging

机译:对中年大鼠巨噬细胞刺激的应变依赖性反应:对健康衰老有用指标的探索

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Rats of Albino Oxford (AO) strain in our animal facility exhibit a longer average healthy life span than rats of Dark Agouit (DA) strain. Since chronic activation of macrophages contributes to chronic low level inflammation common in older age, elucidation of the changes in middle-aged rats could be useful in prevention of unbalanced inflammatory response in advanced age. We have analysed the phenotype of unelicited and thioglycollate-elicited peritoneal macrophages from young and middle-aged DA and AO rats and tested functions of these cells following stimulation with lipopolysaccharide (LPS) in vitro. Unelicited cells from middle-aged DA rats produced higher amounts of proinflammatory mediators interleukin-6 (IL-6) and nitric oxide (NO), but have a diminished response to LPS stimulation then cells from young rats, in spite of increased frequency of TLR4- and CD14-expressing mature macrophages. Injection of thioglycollate robustly increased overall cytokine production in young rats' macrophages, while diminishing their response to LPS stimulation. In middle-aged DA rats injection of thioglycollate diminished IL-6 production, but increased it in response to LPS stimulation. Quite the contrary to DA rats, the macrophages from middle-aged AO rats have released diminished levels of TNF-alpha, and NO, whereas urea production was strongly increased, when compared to the macrophages from young rats. Although the thioglycollate injection has increased the proportion of CD86(+)MHCII(+) mature macrophages in young rats, and percentages of activated TLR4(+) macrophages in both age groups of AO rats, it has not affected the cytokine production in young rats' macrophages, and the TNF-alpha production in middle-aged rats' macrophages. Moreover, the injection of thioglycollate has robustly increased the production of urea in macrophages derived from both age groups of AO rats. Although middle-aged rats of both strains were healthy during experiment, differences between the inflammatory responses of peritoneal macrophages of middle-aged rats of these strains might be one of the contributing factors defining their health in their advanced age. Development of strategies for the prevention of undesirable inflammatory changes in the elderly would benefit from the prospective study of the middle-aged. (C) 2016 Elsevier Inc. All rights reserved.
机译:我们的动物设施中的白化牛津(AO)品系的鼠的平均健康寿命比黑暗Agouit(DA)品系的鼠更长。由于巨噬细胞的慢性激活会导致老年人常见的慢性低水平炎症,因此阐明中年大鼠的变化可能有助于预防高龄者的炎症反应失衡。我们已经分析了来自年轻和中年DA和AO大鼠的未诱发和巯基乙酸诱发的腹膜巨噬细胞的表型,并在体外用脂多糖(LPS)刺激后测试了这些细胞的功能。尽管TLR4的频率增加,但中年DA大鼠的未诱发细胞产生的促炎性介质白介素6(IL-6)和一氧化氮(NO)的量更高,但对LPS刺激的反应却比年轻大鼠的细胞减少。 -和表达CD14的成熟巨噬细胞。注射巯基乙酸盐有力地增加了幼鼠巨噬细胞的总细胞因子产量,同时减少了它们对LPS刺激的反应。在中年DA大鼠中,硫代乙醇酸酯的注射减少了IL-6的产生,但响应LPS刺激而增加了。与DA大鼠相反,与年轻大鼠的巨噬细胞相比,中年AO大鼠的巨噬细胞释放的TNF-α和NO水平降低,而尿素的产生却大大增加。尽管硫代乙醇酸酯注射液增加了两个年龄段的AO大鼠中CD86(+)MHCII(+)成熟巨噬细胞的比例和激活的TLR4(+)巨噬细胞的百分比,但它并未影响年轻大鼠的细胞因子产生巨噬细胞和中年大鼠巨噬细胞的TNF-α产生。此外,硫代乙醇酸酯的注射已强烈增加了来自两个年龄段的AO大鼠的巨噬细胞中尿素的产生。尽管两种品系的中年大鼠在实验中都是健康的,但这些品系的中年大鼠腹膜巨噬细胞炎症反应之间的差异可能是决定其高龄者健康的重要因素之一。中老年人的前瞻性研究将有助于制定预防老年人不良炎症变化的策略。 (C)2016 Elsevier Inc.保留所有权利。

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