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结核分枝杆菌诱导的激活加速活动性肺结核患者外周血中性粒细胞的凋亡。

Mycobacterium tuberculosis-induced activation accelerates apoptosis in peripheral blood neutrophils from patients with active tuberculosis.

作者信息

Alemán Mercedes, García Ana, Saab María A, De La Barrera Silvia S, Finiasz Marta, Abbate Eduardo, Sasiain María C

机构信息

Departamento de Inmunología, Instituto de Investigaciones Hematológicas, Academia Nacional de Medicina, Buenos Aires, Argentina.

出版信息

Am J Respir Cell Mol Biol. 2002 Nov;27(5):583-92. doi: 10.1165/rcmb.2002-0038OC.

DOI:10.1165/rcmb.2002-0038OC
PMID:12397018
Abstract

The activation of circulating polymorphonuclear neutrophils (PMN) from patients with active tuberculosis (TB-PMN) may be associated with induction of apoptosis. Spontaneous or Mycobacterium tuberculosis (MTB)-induced apoptosis of PMN were evaluated by microscopy, DNA content, and their binding to Annexin V at 0, 3, and 18 h. In addition, the expression of CD11b and of CD16 were evaluated as parameters of activation and apoptosis, respectively. Recently isolated TB-PMN showed a higher CD11b expression than normal PMN (N-PMN), but there were no features of apoptosis, even though an enhancement of Fas expression was observed. Spontaneous apoptosis was accelerated in TB-PMN at 3 h, but no differences were observed in TB- and N-PMN at 18 h of culture. When stimulated with MTB, both TB- and N-PMN steadily increased CD11b expression along the culture period. MTB induced apoptosis of N-PMN at 3 h with loss of CD16 expression. By contrast, MTB delayed the apoptotic rate of TB-PMN, preserving the CD16 receptor at 3 h, whereas it accelerated apoptosis at 18 h, increasing at the same time the expression of CD11b. Taken together, these data suggest that the acceleration of apoptosis observed in TB-PMN could be associated with the MTB-induced activation.

摘要

活动性肺结核患者循环中的多形核中性粒细胞(TB-PMN)的激活可能与细胞凋亡的诱导有关。通过显微镜检查、DNA含量以及在0、3和18小时时它们与膜联蛋白V的结合情况,评估PMN的自发凋亡或结核分枝杆菌(MTB)诱导的凋亡。此外,分别评估CD11b和CD16的表达作为激活和凋亡的参数。最近分离的TB-PMN显示出比正常PMN(N-PMN)更高的CD11b表达,但即使观察到Fas表达增强,也没有凋亡特征。TB-PMN在3小时时自发凋亡加速,但在培养18小时时,TB-PMN和N-PMN之间没有差异。当用MTB刺激时,TB-PMN和N-PMN在整个培养期间CD11b表达均稳步增加。MTB在3小时时诱导N-PMN凋亡,同时CD16表达丧失。相比之下,MTB延迟了TB-PMN的凋亡率,在3小时时保留了CD16受体,而在18小时时加速了凋亡,同时增加了CD11b的表达。综上所述,这些数据表明,在TB-PMN中观察到的凋亡加速可能与MTB诱导的激活有关。

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