Time-dependent effect of E-coli LPS in spleen DC activation in vivo: Alteration of numbers, expression of co-stimulatory molecules, production of pro-inflammatory cytokines, and presentation of antigens

被引:22
作者
Xu, Li [1 ]
Kwak, Minseok [2 ]
Zhang, Wei [1 ]
Lee, Peter Chang-Whan [3 ]
Jin, Jun-O. [1 ]
机构
[1] Fudan Univ, Shanghai Med Coll, Shanghai Publ Hlth Clin Ctr, Shanghai, Peoples R China
[2] Pukyong Natl Univ, Dept Chem, Busan, South Korea
[3] Univ Ulsan, Dept Biomed Sci, ASAN Med Ctr, Coll Med, Seoul, South Korea
基金
中国国家自然科学基金;
关键词
LPS; Dendritic cells; Maturation; Co-stimulatory molecules; Pro-inflammatory cytokine; Antigen presentation; DENDRITIC CELL MATURATION; CROSS-PRESENTATION; T-CELLS; IMMUNITY; SEPSIS; SUBSET; TOLERANCE; VACCINES; KINASE; CD8(+);
D O I
10.1016/j.molimm.2017.02.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lipopolysaccharide (LPS) is a well-known stimuli of dendritic cells (DCs). However, in vivo spleen DC maturation by Escherichia coli (E.coli) LPS has not been fully investigated. In this study, we examined the effect of LPS on the activation of spleen DCs and its subsets in a time-dependent manner on mice in vivo. The frequency, number and migration of spleen conventional DCs (cDCs) were increased 6 and 12 h after completion of LPS treatment. Those increased DC numbers in spleen were then gradually decreased with apoptosis of the DCs. The highest levels of co-stimulatory molecule expression in the spleen cDCs and their subsets occurred 18 h after LPS treatment, while the pro-inflammatory cytokines reached their maximum in the intracellular levels of the spleen cDCs and their subsets 3 h after LPS treatment. The antigen presentation of the spleen cDCs and their subsets increased gradually from 3 to 12 h after LPS treatment, but those levels decreased rapidly after 18 h post-LPS treatment. Thus, by highlighting the importance of time in the stimulation of spleen DCs by LPS in mice in vivo, our data provided a model that could be used by immunologists when considering the manipulation of DC functions in vivo for experimental and clinical applications. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:205 / 213
页数:9
相关论文
共 35 条
[1]   Lipopolysaccharide-Activated Dendritic Cells: "Exhausted" or Alert and Waiting? [J].
Abdi, Kaveh ;
Singh, Nevil J. ;
Matzinger, Polly .
JOURNAL OF IMMUNOLOGY, 2012, 188 (12) :5981-5989
[2]   Septic shock [J].
Annane, D ;
Bellissant, E ;
Cavaillon, JM .
LANCET, 2005, 365 (9453) :63-78
[3]   The PI3 kinase, p38 SAP kinase, and NF-κB signal transduction pathways are involved in the survival and maturation of lipopolysaccharide-stimulated human monocyte-derived dendritic cells [J].
Ardeshna, KM ;
Pizzey, AR ;
Devereaux, S ;
Khwaja, A .
BLOOD, 2000, 96 (03) :1039-1046
[4]   Dendritic cells and the control of immunity [J].
Banchereau, J ;
Steinman, RM .
NATURE, 1998, 392 (6673) :245-252
[5]   Dendritic cells as therapeutic vaccines against cancer [J].
Banchereau, J ;
Palucka, AK .
NATURE REVIEWS IMMUNOLOGY, 2005, 5 (04) :296-306
[6]   The Role of Natural Killer Cells in Sepsis [J].
Chiche, Laurent ;
Forel, Jean-Marie ;
Thomas, Guillemette ;
Farnarier, Catherine ;
Vely, Frederic ;
Blery, Mathieu ;
Papazian, Laurent ;
Vivier, Eric .
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY, 2011,
[7]   Dendritic cell-targeted vaccines [J].
Cohn, Lillian ;
Delamarre, Lelia .
FRONTIERS IN IMMUNOLOGY, 2014, 5
[8]   A subset of toll-like receptor ligands induces cross-presentation by bone marrow-derived dendritic cells [J].
Datta, SK ;
Redecke, V ;
Prilliman, KR ;
Takabayashi, K ;
Corr, M ;
Tallant, T ;
DiDonato, J ;
Dziarski, R ;
Akira, S ;
Schoenberger, SP ;
Raz, E .
JOURNAL OF IMMUNOLOGY, 2003, 170 (08) :4102-4110
[9]   Regulation of dendritic cell numbers and maturation by lipopolysaccharide in vivo [J].
DeSmedt, T ;
Pajak, B ;
Muraille, E ;
Lespagnard, L ;
Heinen, E ;
DeBaetselier, P ;
Urbain, J ;
Leo, O ;
Moser, M .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 184 (04) :1413-1424
[10]   Sepsis and the dendritic cell [J].
Efron, P ;
Moldawer, LL .
SHOCK, 2003, 20 (05) :386-401