Interferon-γ signal transduction during parasite infection:: modulation of MAP kinases in the infection of human monocyte cells (THP1) by Toxoplasma gondii
被引:16
作者:
Gomez-Marin, JE
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Gomez-Marin, JE
Valere, A
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Valere, A
Bonhomme, A
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Bonhomme, A
El'btaouri, H
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
El'btaouri, H
Antonicelli, F
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Antonicelli, F
Burlet, H
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Burlet, H
Aubert, D
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Aubert, D
Villena, I
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Villena, I
Guenounou, M
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Guenounou, M
Haye, B
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Haye, B
Pinon, JM
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机构:CHRU, Lab Parasitol Mycol, F-51092 Reims, France
Pinon, JM
机构:
[1] CHRU, Lab Parasitol Mycol, F-51092 Reims, France
[2] CHRU, INSERM, U314, F-51092 Reims, France
[3] Univ Nacl Colombia, Hosp San Juan Dios, Dept Med Interna, Grp Patol Infecc, Santafe Bogota DC, Colombia
[4] Univ Reims, Biochim Lab, CNRS, Unite UPRES A 6021, F-51687 Reims, France
[5] Univ Reims, Fac Pharm, Immunol Lab, F-51100 Reims, France
[6] Univ Reims, Fac Pharm, Ctr Biomol IFR 53, F-51100 Reims, France
human monocytes;
T;
gondii;
IFN-gamma;
MAP kinase;
D O I:
10.1046/j.1365-3024.1998.00194.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
We assayed mitogen-activated protein (MAP) kinase phosphorylation in a human monocyte cell line (THP1) during their infection by Toxoplasma gondii. In addition, we tested the effect of specific MAP kinase inhibitors (PD098059 and SB203580) on parasite invasion. MAP kinase phosphorylation was increased in the cytosol and membrane fractions of THP1 infected with T. gondii. The MAP kinase phosphorylation of uninfected THP1 cells was not significantly modified by incubation for 20 h with 1000 U/ml of IFN-gamma. However, IFN-gamma treatment of infected cells significantly reduces the increase in phosphorylation. caused by parasite infection, There was also MAP kinase activity in the cytosol and membrane fractions of extracellular T. gondii tachyzoites. IFN-gamma altered the distribution of activity in subcellular fractions of extracellular T. gondii tachyzoites. This indicates that IFN-gamma directly affects parasite MAP kinase activity. The results provide evidence that MAP kinase pathways participate in the infection by T. gondii and that the decrease in MAP kinase activity in infected cells caused by IFN-gamma may be involved in mediating their protective signals.