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老年中性粒细胞细胞骨架组装能力和氧化反应的调节

Modulation of cytoskeleton assembly capacity and oxidative response in aged neutrophils.

作者信息

Piazzolla G, Tortorella C, Serrone M, Jirillo E, Antonaci S

机构信息

Department of Internal Medicine, Immunology and Infectious Diseases, University of Bari Medical School, Italy.

出版信息

Immunopharmacol Immunotoxicol. 1998 May;20(2):251-66. doi: 10.3109/08923979809038543.

Abstract

Several reports have emphasized that aged polymorphonuclear cells (PMN) exhibit an impairment of superoxide anion (O2-) generation when triggered with formyl-methionyl-leucine-phenylalanine (FMLP) in comparison to the younger counterpart. Since microfilaments and microtubules are involved in PMN-mediated functions, in a group of old donors we assessed the effects of either actin stabilizing and disrupting agents, i.e. phalloidin and cytochalasin B, or microtubule stabilization or disruption by taxol and colchicine, respectively, on FMLP-triggered neutrophil oxidative responsiveness. Results show that phalloidin treatment, at a concentration ranging from 10(-6) to 10(-8) M, gave rise to an inhibition of O2- release by aged PMN, while the same effect was seen in similarly treated young cells at a concentration of 10(-7) M only. On the contrary, cytochalasin B pretreatment led to an enhancement of O2- generation in both young and aged neutrophils, even if to a lower extent in the latter group. At the same time, taxol at 10(-8) M strength inhibited young cell responsiveness, while no effects were induced by colchicine treatment. Quite interestingly, elderly neutrophil function was negatively modulated by both microtubule affecting compounds. Altogether, these findings suggest the possible relevance of cytoskeletal affecting compounds in the modulation of FMLP-stimulated O2- release during senescence.

摘要

几份报告强调,与年轻的多形核细胞(PMN)相比,衰老的PMN在受到甲酰甲硫氨酰亮氨酰苯丙氨酸(FMLP)刺激时,超氧阴离子(O2-)生成受损。由于微丝和微管参与PMN介导的功能,我们在一组老年供体中评估了肌动蛋白稳定和破坏剂(即鬼笔环肽和细胞松弛素B),或分别用紫杉醇和秋水仙碱进行微管稳定或破坏,对FMLP触发的中性粒细胞氧化反应性的影响。结果表明,在10(-6)至10(-8)M的浓度范围内,鬼笔环肽处理会抑制衰老PMN释放O2-,而在同样处理的年轻细胞中,只有在10(-7)M的浓度下才会出现相同的效果。相反,细胞松弛素B预处理会导致年轻和衰老中性粒细胞中O2-生成增加,尽管后一组增加的程度较低。同时,10(-8)M浓度的紫杉醇抑制年轻细胞的反应性,而秋水仙碱处理则没有诱导任何影响。非常有趣的是,微管影响化合物对老年中性粒细胞功能有负面调节作用。总之,这些发现表明细胞骨架影响化合物在衰老过程中对FMLP刺激的O2-释放的调节中可能具有相关性。

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