Streptococcus pyogenes induces oncosis in macrophages through the activation of an inflammatory programmed cell death pathway

被引:75
作者
Goldmann, Oliver [1 ]
Sastalla, Inka
Wos-Oxley, Melissa [2 ]
Rohde, Manfred
Medina, Eva [1 ]
机构
[1] HZI Helmholtz Ctr Infect Res, Dept Microbial Pathogenesis, Infect Immunol Res Grp, Braunschweig, Germany
[2] HZI Helmholtz Ctr Infect Res, Dept Microbial Pathogenesis, Biodegradat Grp, Braunschweig, Germany
关键词
MITOCHONDRIAL PERMEABILITY TRANSITION; GROUP-A STREPTOCOCCI; SINUSOIDAL ENDOTHELIAL-CELLS; MONOCYTE-DERIVED MACROPHAGES; STREPTOLYSIN-O; EPITHELIAL-CELLS; INFECTED MACROPHAGES; CHEMICAL HYPOXIA; OSMOTIC LYSIS; IN-VITRO;
D O I
10.1111/j.1462-5822.2008.01245.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Macrophages are crucial components of the host defence against Streptococcus pyogenes. Here, we demonstrate the ability of S. pyogenes to kill macrophages through the activation of an inflammatory programmed cell death pathway. Macrophages exposed to S. pyogenes exhibited extensive cytoplasmic vacuolization, cellular and organelle swelling and rupture of the plasma membrane typical of oncosis. The cytotoxic effect of S. pyogenes on macrophages is mediated by the streptococcal cytolysins streptolysin S and streptolysin O and does not require bacterial internalization. S. pyogenes-induced death of macrophages was not affected by the addition of osmoprotectant, implicating the activation of an orchestrated cell death pathway rather than a simple osmotic lysis. This programme cell death pathway involves the loss of mitochondria transmembrane potential (Delta psi(m)) and was inhibited by the addition of exogenous glycine, which has been shown to prevent necrotic cell death by blocking the opening of death channels in the plasma membrane. The production of reactive oxygen species and activation of calpains were identified as mediators of the cell death process. We conclude that activation of the inflammatory programmed cell death pathway in macrophages could constitute an important pathogenic mechanism by which S. pyogenes evades host immune defences and causes disease.
引用
收藏
页码:138 / 155
页数:18
相关论文
共 58 条
[21]  
GOOT VD, 2001, PORE FORMING TOXINS
[22]  
GUNTER TE, 1990, AM J PHYSIOL, V755, pC786
[23]   EVIDENCE THAT CLOSTRIDIUM-PERFRINGENS THETA-TOXIN INDUCES COLLOID-OSMOTIC LYSIS OF ERYTHROCYTES [J].
HARRIS, RW ;
SIMS, PJ ;
TWETEN, RK .
INFECTION AND IMMUNITY, 1991, 59 (07) :2499-2501
[24]   Effect of a bacterial pheromone peptide on host chemokine degradation in group A streptococcal necrotising soft-tissue infections [J].
Hidalgo-Grass, C ;
Dan-Goor, M ;
Maly, A ;
Eran, Y ;
Kwinn, LA ;
Nizet, V ;
Ravins, M ;
Jaffe, J ;
Peyser, A ;
Moses, AE ;
Hanski, E .
LANCET, 2004, 363 (9410) :696-703
[25]   EFFECT OF STREPTOLYSIN-S ON HUMAN AND MOUSE T AND B LYMPHOCYTES [J].
HRYNIEWICZ, W ;
PRYJMA, J .
INFECTION AND IMMUNITY, 1977, 16 (03) :730-733
[26]   Salmonella-induced caspase-2 activation in macrophages:: A novel mechanism in pathogen-mediated apoptosis [J].
Jesenberger, V ;
Procyk, KJ ;
Yuan, JY ;
Reipert, S ;
Baccarini, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (07) :1035-1045
[27]   Mitochondrial permeability transition: a common pathway to necrosis and apoptosis [J].
Kim, JS ;
He, LH ;
Lemasters, JJ .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 304 (03) :463-470
[28]   Role of the mitochondrial permeability transition in apoptotic and necrotic death after ischemia/reperfusion injury to hepatocytes [J].
Kim, JS ;
He, L ;
Qian, T ;
Lemasters, JJ .
CURRENT MOLECULAR MEDICINE, 2003, 3 (06) :527-535
[29]   Mitochondrial control of cell death [J].
Kroemer, G ;
Reed, JC .
NATURE MEDICINE, 2000, 6 (05) :513-519
[30]   Intracellular adenosine triphosphate (ATP) concentration: A switch in the decision between apoptosis and necrosis [J].
Leist, M ;
Single, B ;
Castoldi, AF ;
Kuhnle, S ;
Nicotera, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (08) :1481-1486