CRL-1072 enhances antimycobacterial activity of human macrophages through interleukin-8

被引:17
作者
Jagannath, C [1 ]
Pai, S [1 ]
Actor, JK [1 ]
Hunter, RL [1 ]
机构
[1] Univ Texas, Sch Med, Dept Pathol & Lab Med, Ctr Hlth Sci, Houston, TX 77030 USA
关键词
D O I
10.1089/107999099314432
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CRL-1072 is a poloxamer surfactant that kills mycobacteria more effectively within macrophages than in broth cultures. Human macrophages treated with CRL-1072 synthesized interleukin-8 (IL-8), tumor necrosis factor-alpha (TNF-alpha), and granulocyte-macrophage colony-stimulating factor (GM-CSF) in a dose-dependent manner. About 3000 pg of IL-8 per million human macrophages accumulated in cultures treated with 100-1500 ng of poloxamer, with mRNA message for IL-8 induced as early as 2 h, As macrophages do not have IL-RA receptors, a transwell culture was used to study the chemotactic and activating effects of IL-8 between CRL-1072-treated human macrophage effecters and polymorphonuclear neutrophil (PMN) targets. PMN were activated by IL-8 and secreted hydrogen peroxide and myeloperoxidase (MPO), MPO derived from PMN, in turn, activated monocytes for an enhanced killing of intracellular Mycobacterium avium, The ability of CRL-1072 to modulate macrophage-mediated activation of neutrophils and receive a feedback activation signal may form one mechanism by which its antimycobacterial activity is achieved in vivo.
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收藏
页码:67 / 76
页数:10
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