Suppr超能文献

[不同抗结核药物对吞噬体与溶酶体融合、小鼠腹腔巨噬细胞中F-肌动蛋白含量及体外G-肌动蛋白聚合的影响]

[The effect of different antitubercular agents on phagosome fusion with lysosomes, on the F-actin content in mouse peritoneal macrophages and on G-actin polymerization in vitro].

作者信息

Mozhenok T P, Solov'eva L V, Braun A D, Bulychev A G

出版信息

Tsitologiia. 1994;36(11):1123-8.

PMID:7709472
Abstract

Effects of various antituberculosis remedies (ATR)--isoniazid (INA), saluzid (SA), streptosaluzid (SS), ethambutol (EB), sodium para-aminosalicylate (SPAS) on phagosome-lysosome (PL) fusion, on F-actin content in mouse macrophages and on G-actin polymerization in vitro were studied. The ATR of choice have been shown to stimulate the PL fusion. INA (0.2 mM), SA (0.02 mM), SS (0.05 mM), EB (0.08 mM) and SPAS (0.5 mM) increased the F-actin content and changed its localization within macrophages. ATR changed the character of G-actin polymerization in vitro. Possible mechanisms of interrelation between cytoskeleton (actin part) changes and PL fusion are discussed. The results obtained suggest to use the ATR-induced changes in PL fusion and F-actin content in the cells for estimating therapeutic effects of respective antituberculosis remedies.

摘要

研究了各种抗结核药物(ATR)——异烟肼(INA)、柳氮磺胺吡啶(SA)、链柳氮磺胺吡啶(SS)、乙胺丁醇(EB)、对氨基水杨酸钠(SPAS)对吞噬体-溶酶体(PL)融合、小鼠巨噬细胞中F-肌动蛋白含量以及体外G-肌动蛋白聚合的影响。已证明所选用的抗结核药物能刺激PL融合。INA(0.2 mM)、SA(0.02 mM)、SS(0.05 mM)、EB(0.08 mM)和SPAS(0.5 mM)增加了F-肌动蛋白含量,并改变了其在巨噬细胞内的定位。抗结核药物在体外改变了G-肌动蛋白聚合的特性。讨论了细胞骨架(肌动蛋白部分)变化与PL融合之间相互关系的可能机制。所得结果表明,可利用抗结核药物诱导的细胞内PL融合和F-肌动蛋白含量变化来评估相应抗结核药物的治疗效果。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验