Differential activation of NF-κB subunits in dendritic cells in response to Gram-negative bacteria and to lipopolysaccharide

被引:46
作者
Hofer, S
Rescigno, M
Granucci, F
Citterio, S
Francolini, M
Ricciardi-Castagnoli, P
机构
[1] Univ Milan, Dept Biosci & Biotechnol, I-20126 Milan, Italy
[2] CNR, Cellular & Mol Pharmacol Ctr, I-20129 Milan, Italy
关键词
dendritic cells; NF-kappa B; Salmonella typhimurium; signal transduction; maturation;
D O I
10.1016/S1286-4579(01)01378-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cell (DC) maturation is essential for the initiation of T-dependent immune responses. Nuclear factor kappaB/Rel (NF kappaB/Rel) transcription factors are ubiquitously expressed signalling molecules, known to regulate the transcription of a large number of genes involved in immune responses, including cytokines such as IL-1, IL-6, TNF-alpha and cell surface molecules (MHC class I and II, B7.2). In this study, we have compared the activation of five members of the NF-kappaB family, p65, c-Rel, p50, RelB and p52, during DC maturation in response to lipopolysaccharide (LPS) and to Salmonella typhimurium. We have shown that although the translocation of NF-kappaB occurred very early, 30 min after treatment with both S. typhimurium and LPS, bacteria-induced NF-kappaB activation was more pronounced. Four out of five members, i.e. p65, c-Rel, p50 and RelB, were similarly activated upon the two stimuli but with different kinetics. Indeed, we have observed that p65, c-Rel and p50 were translocated early, whereas RelB was translocated later in DC activation. This differential regulation suggests that the various members of NF-kappaB family can mediate distinct functions of DC physiology. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
引用
收藏
页码:259 / 265
页数:7
相关论文
共 34 条
[1]   Differential expression of the transcription factor NF-κB during human mononuclear phagocyte differentiation to macrophages and dendritic cells [J].
Ammon, C ;
Mondal, K ;
Andreesen, R ;
Krause, SW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 268 (01) :99-105
[2]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[3]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[4]   EMBRYONIC LETHALITY AND LIVER DEGENERATION IN MICE LACKING THE RELA COMPONENT OF NF-KAPPA-B [J].
BEG, AA ;
SHA, WC ;
BRONSON, RT ;
GHOSH, S ;
BALTIMORE, D .
NATURE, 1995, 376 (6536) :167-170
[5]   EXPRESSION OF RELB IS REQUIRED FOR THE DEVELOPMENT OF THYMIC MEDULLA AND DENDRITIC CELLS [J].
BURKLY, L ;
HESSION, C ;
OGATA, L ;
REILLY, C ;
MARCONI, LA ;
OLSON, D ;
TIZARD, R ;
CATE, R ;
LO, D .
NATURE, 1995, 373 (6514) :531-536
[6]   Nuclear factor (NF)-κB2 (p100/p52) is required for normal splenic microarchitecture and B cell-mediated immune responses [J].
Caamaño, JH ;
Rizzo, CA ;
Durham, SK ;
Barton, DS ;
Raventós-Suárez, C ;
Snapper, CM ;
Bravo, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (02) :185-196
[7]   Multiple hemopoietic defects and lymphoid hyperplasia in mice lacking the transcriptional activation domain of the c-rel protein [J].
Carrasco, D ;
Cheng, J ;
Lewin, A ;
Warr, G ;
Yang, HY ;
Rizzo, C ;
Rosas, F ;
Snapper, C ;
Bravo, R .
JOURNAL OF EXPERIMENTAL MEDICINE, 1998, 187 (07) :973-984
[8]  
Clark GJ, 1999, IMMUNOLOGY, V98, P189
[9]   Absence of tumor necrosis factor rescues RelA-deficient mice from embryonic lethality [J].
Doi, TS ;
Marino, MW ;
Takahashi, T ;
Yoshida, T ;
Sakakura, T ;
Old, LJ ;
Obata, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (06) :2994-2999
[10]   Upon dendritic cell (DC) activation chemokines and chemokine receptor expression are rapidly regulated for recruitment and maintenance of DC at the inflammatory site [J].
Foti, M ;
Granucci, F ;
Aggujaro, D ;
Liboi, E ;
Luini, W ;
Minardi, S ;
Mantovani, A ;
Sozzani, S ;
Ricciardi-Castagnoli, P .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (06) :979-986