Foamy macrophages within lung granulomas of mice infected with Mycobacterium tuberculosis express molecules characteristic of dendritic cells and antiapoptotic markers of the TNF receptor-associated factor family

被引:86
作者
Ordway, D [1 ]
Henao-Tamayo, M [1 ]
Orme, IM [1 ]
Gonzalez-Juarrero, M [1 ]
机构
[1] Colorado State Univ, Dept Microbiol Immunol & Pathol, Mycobacteria Res Labs, Ft Collins, CO 80523 USA
关键词
D O I
10.4049/jimmunol.175.6.3873
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Highly vacuolated or foamy macrophages are a distinct characteristic of granulomas in the lungs of animals infected with Mycobacterium tuberculosis. To date these have usually been considered to represent activated macrophages derived from monocytes entering the lesions from the blood. However, we demonstrate in this study that foamy macrophages express high levels of DEC-205, a marker characteristic of dendritic cells (DCs). In addition to high expression of the DEC-205 marker, these cells were characterized as CD11b+CD11c(high)MHC class IIhigh, and CD40(high), which are additional markers typically expressed by DCs. Up-regulation of CD40 was seen only during the early chronic stage of the lung disease, and both the expression of CD40 and MHC class II markers were down-regulated as the disease progressed into the late chronic phase. Foamy cells positive for the DEC-205 marker also expressed high levels of TNFR-associated factor-1 (TRAF-1), TRAF-2, and TRAF-3, markers associated with resistance to apoptosis. These data indicate that in addition to the central role of DCs in initiating the acquired immune response against M. tuberculosis infection, they also participate in the granulomatous response.
引用
收藏
页码:3873 / 3881
页数:9
相关论文
共 69 条
[1]   THE SPECIFIC RECOGNITION BY MACROPHAGES OF CD8(+),CD45RO(+) T-CELLS UNDERGOING APOPTOSIS - A MECHANISM FOR T-CELL CLEARANCE DURING RESOLUTION OF VIRAL-INFECTIONS [J].
AKBAR, AN ;
SAVILL, J ;
GOMBERT, W ;
BOFILL, M ;
BORTHWICK, NJ ;
WHITELAW, F ;
GRUNDY, J ;
JANOSSY, G ;
SALMON, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (05) :1943-1947
[2]   Increased dendritic cell numbers impair protective immunity to intracellular bacteria despite augmenting antigen-specific CD8+ T lymphocyte responses [J].
Alaniz, RC ;
Sandall, S ;
Thomas, EK ;
Wilson, CB .
JOURNAL OF IMMUNOLOGY, 2004, 172 (06) :3725-3735
[3]  
Algood HMS, 2004, J IMMUNOL, V173, P3287
[4]   Tumor necrosis factor receptor-associated factors (TRAFs) - a family of adaptor proteins that regulates life and death [J].
Arch, RH ;
Gedrich, RW ;
Thompson, CB .
GENES & DEVELOPMENT, 1998, 12 (18) :2821-2830
[5]  
Balcewicz-Sablinska MK, 1998, J IMMUNOL, V161, P2636
[6]   Fate of Mycobacterium tuberculosis within murine dendritic cells [J].
Bodnar, KA ;
Serbina, NV ;
Flynn, JL .
INFECTION AND IMMUNITY, 2001, 69 (02) :800-809
[7]   In vivo targeting of antigens to maturing dendritic cells via the DEC-205 receptor improves T cell vaccination [J].
Bonifaz, LC ;
Bonnyay, DP ;
Charalambous, A ;
Darguste, DI ;
Fujii, SI ;
Soares, H ;
Brimnes, MK ;
Moltedo, B ;
Moran, TM ;
Steinman, RM .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (06) :815-824
[8]  
BOWEN ID, 1990, PROGRAMMED CELL DEAT, P15
[9]   DISSEMINATED TUBERCULOSIS IN INTERFERON-GAMMA GENE-DISRUPTED MICE [J].
COOPER, AM ;
DALTON, DK ;
STEWART, TA ;
GRIFFIN, JP ;
RUSSELL, DG ;
ORME, IM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1993, 178 (06) :2243-2247
[10]   THE PROTECTIVE IMMUNE-RESPONSE TO MYCOBACTERIUM-TUBERCULOSIS [J].
COOPER, AM ;
FLYNN, JL .
CURRENT OPINION IN IMMUNOLOGY, 1995, 7 (04) :512-516