Intestinal dendritic cells change in number in fulminant hepatic failure

被引:5
作者
Cao, Xu [1 ,2 ]
Liu, Mei [1 ,2 ]
Wang, Peng [1 ,2 ]
Liu, Dong-Yan [1 ,2 ]
机构
[1] China Med Univ, Shengjing Hosp, Res Ctr, Shenyang 110004, Liaoning Provin, Peoples R China
[2] Minist Hlth, Key Lab Congenital Malformat Res, Shenyang 110004, Liaoning Provin, Peoples R China
基金
中国国家自然科学基金;
关键词
Fulminant hepatic failure; Intestinal dendritic cells; MHC II; CD3; AKT/Phosphorylated-AKT; GUT EPITHELIAL MONOLAYERS; SIGNALING PATHWAY; INVARIANT CHAIN; BACTERIA; HOMEOSTASIS; INFLAMMATION; EXPRESSION; INJURY; PERMEABILITY; MODULATION;
D O I
10.3748/wjg.v21.i16.4883
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
AIM: To investigate the change in intestinal dendritic cell (DC) number in fulminant hepatic failure (FHF). METHODS: An animal model of FHF was created. Intestinal CD11b/c was detected by immunohisto-chemistry and Western blot. Quantitative real-time polymerase chain reaction (PCR) was used to detect intestinal integrin-alpha mRNA expression. Intestinal CD83, CD86, CD74, CD3 and AKT were detected by immunohistochemistry, Western blot and PCR. Phosphorylated-AKT (p-AKT) was detected by immunohistochemistry and Western blot. RESULTS: In the FHF group [D-galactosamine (D-Galn) + lipopolysaccharide (LPS) group], the mice began to die after 6 h; conversely, in the D-Galn and LPS groups, the activity of mice was poor, but there were no deaths. Immunohistochemistry results showed that in FHF, the expression of CD11b/c (7988400 +/- 385941 vs 1102400 +/- 132273, P < 0.05), CD83 (13875000 +/- 467493 vs 9257600 +/- 400364, P < 0.05), CD86 (7988400 +/- 385941 vs 1102400 +/- 13227, P < 0.05) and CD74 (11056000 +/- 431427 vs 4633400 +/- 267903, P < 0.05) was significantly increased compared with the normal saline (NS) group. Compared with the NS group, the protein expression of CD11b/c (5.4817 +/- 0.77 vs 1.4073 +/- 0.37, P < 0.05) and CD86 (4.2673 +/- 0.69 vs 1.1379 +/- 0.42, P < 0.05) was significantly increased. Itg-alpha (1.1224 +/- 0.3 vs 0.4907 +/- 0.19, P < 0.05), CD83 (3.6986 +/- 0.40 vs 1.0762 +/- 0.22, P < 0.05) and CD86 (1.5801 +/- 0.32 vs 0.8846 +/- 0.10, P < 0.05) mRNA expression was increased significantly in the FHF group. At the protein level, expression of CD74 in the FHF group (2.3513 +/- 0.52) was significantly increased compared with the NS group (1.1298 +/- 0.33), whereas in the LPS group (2.3891 +/- 0.47), the level of CD74 was the highest (P < 0.05). At the gene level, the relative expression of CD74 mRNA in the FHF group (1.5383 +/- 0.26) was also significantly increased in comparison to the NS group (0.7648 +/- 0.22; P < 0.05). CD3 expression was the highest in the FHF group (P < 0.05). In the FHF, LPS and D-Galn groups, the expression of AKT at the protein and mRNA levels was elevated compared with the NS group, but there was no statistical significance (P > 0.05). The p-AKT protein expression in the FHF (1.54 +/- 0.06), LPS (1.56 +/- 0.05) and D-Galn (1.29 +/- 0.03) groups was higher than that in the NS group (1.07 +/- 0.03) (P < 0.05). CONCLUSION: In FHF, a large number of DCs mature, express CD86, and activate MHC class. molecular pathways to induce a T cell response, and the AKT pathway is activated.
引用
收藏
页码:4883 / 4893
页数:11
相关论文
共 41 条
[1]
IL-1β-Induced Increase in Intestinal Epithelial Tight Junction Permeability Is Mediated by MEKK-1 Activation of Canonical NF-κB Pathway [J].
Al-Sadi, Rana ;
Ye, Dongmei ;
Said, Hamid M. ;
Ma, Thomas Y. .
AMERICAN JOURNAL OF PATHOLOGY, 2010, 177 (05) :2310-2322
[2]
A CD74-dependent MHC class I endolysosomal cross-presentation pathway [J].
Basha, Genc ;
Omilusik, Kyla ;
Chavez-Steenbock, Ana ;
Reinicke, Anna T. ;
Lack, Nathan ;
Choi, Kyung Bok ;
Jefferies, Wilfred A. .
NATURE IMMUNOLOGY, 2012, 13 (03) :237-U53
[3]
Dendritic cell CD83 homotypic interactions regulate inflammation and promote mucosal homeostasis [J].
Bates, J. M. ;
Flanagan, K. ;
Mo, L. ;
Ota, N. ;
Ding, J. ;
Ho, S. ;
Liu, S. ;
Roose-Girma, M. ;
Warming, S. ;
Diehl, L. .
MUCOSAL IMMUNOLOGY, 2015, 8 (02) :414-428
[4]
The intramembrane protease Sppl2a is required for B cell and DC development and survival via cleavage of the invariant chain [J].
Beisner, Daniel R. ;
Langerak, Petra ;
Parker, Albert E. ;
Dahlberg, Carol ;
Otero, Francella J. ;
Sutton, Sue E. ;
Poirot, Laurent ;
Barnes, Whitney ;
Young, Michael A. ;
Niessen, Sherry ;
Wiltshire, Tim ;
Bodendorf, Ursula ;
Martoglio, Bruno ;
Cravatt, Benjamin ;
Cooke, Michael P. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2013, 210 (01) :23-30
[5]
Therapeutic Potential of Tolerogenic Dendritic Cells in IBD: From Animal Models to Clinical Application [J].
Cabezon, Raquel ;
Benitez-Ribas, Daniel .
CLINICAL & DEVELOPMENTAL IMMUNOLOGY, 2013,
[6]
Lactobacilli differentially modulate expression of cytokines and maturation surface markers in murine dendritic cells [J].
Christensen, HR ;
Frokiær, H ;
Pestka, JJ .
JOURNAL OF IMMUNOLOGY, 2002, 168 (01) :171-178
[7]
Deng Xiaohua, 2014, Adv Alzheimer Dis, V3, P78
[8]
Bacterial probiotic modulation of dendritic cells [J].
Drakes, M ;
Blanchard, T ;
Czinn, S .
INFECTION AND IMMUNITY, 2004, 72 (06) :3299-3309
[9]
Soluble CD83 ameliorates experimental colitis in mice [J].
Eckhardt, J. ;
Kreiser, S. ;
Doebbeler, M. ;
Nicolette, C. ;
DeBenedette, M. A. ;
Tcherepanova, I. Y. ;
Ostalecki, C. ;
Pommer, A. J. ;
Becker, C. ;
Guenther, C. ;
Zinser, E. ;
Mak, T. W. ;
Steinkasserer, A. ;
Lechmann, M. .
MUCOSAL IMMUNOLOGY, 2014, 7 (04) :1006-1018
[10]
Inhibition of heat-induced apoptosis in rat small intestine and IEC-6 cells through the AKT signaling pathway [J].
Gao, Zhimin ;
Liu, Fenghua ;
Yin, Peng ;
Wan, Changrong ;
He, Shasha ;
Liu, Xiaoxi ;
Zhao, Hong ;
Liu, Tao ;
Xu, Jianqin ;
Guo, Shining .
BMC VETERINARY RESEARCH, 2013, 9