Rapid elimination of Toxoplasma gondii by gamma interferon-primed mouse macrophages is independent of CD40 signaling

被引:29
作者
Zhao, Yanlin [1 ]
Wilson, Douglas [1 ]
Matthews, Suzanne [1 ]
Yap, George S. [1 ]
机构
[1] Brown Univ, Warren Alpert Sch, Dept Mol Microbiol & Immunol, Providence, RI 02912 USA
关键词
D O I
10.1128/IAI.00738-07
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Autophagy has been implicated In the intracellular destruction of Toxoplasma gondii by primed macrophages following gamma Interferon (IFN-gamma) activation of p47 GTPases. CD40 ligation has also been shown to trigger autophagic elimination of T. gondii Independent of IFN-gamma and p47 GTPases. Here we demonstrate that IFN-gamma/p47 GTPase-dependent elimination of T. gondii by strain CPS vaccine-primed macrophages Is independent of CD40/tumor necrosis factor signaling. Similar to wild-type controls, both CD40-deficient and tumor necrosis factor receptor 1/2 (TNFR1/2)-deficient macrophages can efficiently eliminate Invaded strain GFP-PTG and restrain its replication following priming. In contrast, macrophages from mice lacking the IFN-gamma receptor gene neither clear the parasites nor repress their proliferation. Thus, CD40 and IFN-gamma-induced pathogen elimination might represent two independent resistance pathways, the latter of which plays a primary role in anti-Toxoplasma immunity in mice.
引用
收藏
页码:4799 / 4803
页数:5
相关论文
共 28 条
[1]   CD40 signaling in macrophages induces activity against an intracellular pathogen independently of gamma interferon and reactive nitrogen intermediates [J].
Andrade, RM ;
Portillo, JAC ;
Wessendarp, M ;
Subauste, CS .
INFECTION AND IMMUNITY, 2005, 73 (05) :3115-3123
[2]   CD40 induces macrophage anti-Toxoplasma gondii activity by triggering autophagy-dependent fusion of pathogen-containing vacuoles and lysosomes [J].
Andrade, Rosa M. ;
Wessendarp, Matthew ;
Gubbels, Marc-Jan ;
Striepen, Boris ;
Subauste, Carlos S. .
JOURNAL OF CLINICAL INVESTIGATION, 2006, 116 (09) :2366-2377
[3]   The clubfoot assessment protocol (CAP);: description and reliability of a structured multi-level instrument for follow-up -: art. no. 40 [J].
Andriesse, H ;
Hägglund, G ;
Jarnlo, GB .
BMC MUSCULOSKELETAL DISORDERS, 2005, 6 (1)
[4]   The interferon-inducible p47 (IRG) GTPases in vertebrates: loss of the cell autonomous resistance mechanism in the human lineage [J].
Bekpen, C ;
Hunn, JP ;
Rohde, C ;
Parvanova, I ;
Guethlein, L ;
Dunn, DM ;
Glowalla, E ;
Leptin, M ;
Howard, JC .
GENOME BIOLOGY, 2005, 6 (11)
[5]   The p47 GTPases Igtp and Irgb10 map to the Chlamydia trachomatis susceptibility locus Ctrq-3 and mediate cellular resistance in mice [J].
Bernstein-Hanley, Isaac ;
Coers, Jorn ;
Balsara, Zarine R. ;
Taylor, Gregory A. ;
Starnbach, Michael N. ;
Dietrich, William F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2006, 103 (38) :14092-14097
[6]   The role of CD40L in T cell-dependent nitric oxide production by murine macrophages [J].
Bingaman, AW ;
Pearson, TC ;
Larsen, CP .
TRANSPLANT IMMUNOLOGY, 2000, 8 (03) :195-202
[7]  
Boehm U, 1998, J IMMUNOL, V161, P6715
[8]   The human model: A genetic dissection of immunity to infection in natural conditions [J].
Casanova, JL ;
Abel, L .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (01) :55-66
[9]   Inactivation of LRG-47 and IRG-47 reveals a family of interferon γ-inducible genes with essential, pathogen-specific roles in resistance to infection [J].
Collazo, CM ;
Yap, GS ;
Sempowski, GD ;
Lusby, KC ;
Tessarollo, L ;
Woude, GFV ;
Sher, A ;
Taylor, GA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2001, 194 (02) :181-187
[10]  
DeckertSchluter M, 1996, LAB INVEST, V75, P827