Inhibition of Plasmin Protects Against Colitis in Mice by Suppressing Matrix Metalloproteinase 9-Mediated Cytokine Release From Myeloid Cells

被引:38
作者
Munakata, Shinya [1 ,2 ]
Tashiro, Yoshihiko [1 ,2 ]
Nishida, Chiemi [1 ]
Sato, Aki [1 ]
Komiyama, Hiromitsu [1 ,2 ]
Shimazu, Hiroshi [1 ]
Dhahri, Douaa [1 ]
Salama, Yousef [1 ]
Eiamboonsert, Salita [1 ]
Takeda, Kazuyoshi [3 ]
Yagita, Hideo [3 ]
Tsuda, Yuko [5 ]
Okada, Yoshio [5 ]
Nakauchi, Hiromitsu [1 ]
Sakamoto, Kazuhiro [2 ]
Heissig, Beate [1 ,4 ]
Hattori, Koichi [1 ,4 ]
机构
[1] Univ Tokyo, Inst Med Sci, Ctr Stem Cell Biol & Regenerat Med, Minato Ku, Tokyo 1088639, Japan
[2] Juntendo Univ, Sch Med, Dept Coloproctol Surg, Bunkyo Ku, Tokyo 113, Japan
[3] Juntendo Univ, Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 113, Japan
[4] Juntendo Univ, Sch Med, Atopy Allergy Ctr, Bunkyo Ku, Tokyo 113, Japan
[5] Kobe Gakuin Univ, Fac Pharmaceut Sci, Nishi Ku, Kobe, Hyogo 65121, Japan
基金
日本学术振兴会;
关键词
IBD; Mouse Model; Plasminogen; UC; INFLAMMATORY-BOWEL-DISEASE; TUMOR-NECROSIS-FACTOR; VERSUS-HOST-DISEASE; ULCERATIVE-COLITIS; TISSUE REGENERATION; SELECTIVE PLASMIN; ACID THERAPY; FACTOR-ALPHA; FIBRINOLYSIS; COAGULATION;
D O I
10.1053/j.gastro.2014.12.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND & AIMS: Activated proteases such as plasmin and matrix metalloproteinases (MMPs) are activated in intestinal tissues of patients with active inflammatory bowel diseases. We investigated the effect of plasmin on the progression of acute colitis. METHODS: Colitis was induced in Mmp9(-/-), Plg(-/-), and C57BL/6 (control) mice by the administration of dextran sulfate sodium, trinitrobenzene sulfonic acid, or CD40 antibody. Plasmin was inhibited in control mice by intraperitoneal injection of YO-2, which blocks its active site. Mucosal and blood samples were collected and analyzed by reverse-transcription polymerase chain reaction and immunohistochemical analyses, as well as for mucosal inflammation and levels of cytokines and chemokines. RESULTS: Circulating levels of plasmin were increased in mice with colitis, compared with controls. Colitis did not develop in control mice injected with YO-2 or in Plg(-/-) mice. Colons from these mice had reduced infiltration of Gr1+ neutrophils and F4/80+ macrophages, and reduced levels of inflammatory cytokines and chemokines. Colonic inflammation and colitis induction required activation of endogenous MMP9. After colitis induction, mice given YO-2, Plg(-/-) mice, and Mmp9(-/-) mice had reduced serum levels of tumor necrosis factor and C-X-C motif chemokine ligand 5, compared with control mice. CONCLUSIONS: In mice, plasmin induces a feedback mechanism in which activation of the fibrinolytic system promotes the development of colitis via activation of MMP9 or proteolytic enzymes. The proteolytic environment stimulates the influx of myeloid cells into the colonic epithelium and the production of tumor necrosis factor and C-X-C motif chemokine ligand 5. In turn, myeloid CD11b+ cells release the urokinase plasminogen activator, which accelerates plasmin production. Disruption of the plasmin-induced chronic inflammatory circuit therefore might be a strategy for colitis treatment.
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收藏
页码:565 / +
页数:18
相关论文
共 41 条
[1]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[2]   Targeted deletion of metalloproteinase 9 attenuates experimental colitis in mice: Central role of epithelial-derived MMP [J].
Castaneda, FE ;
Walia, B ;
Vijay-Kumar, M ;
Patel, NR ;
Roser, S ;
Kolachala, VL ;
Rojas, M ;
Wang, LX ;
Oprea, G ;
Garg, P ;
Gewirtz, AT ;
Roman, J ;
Merlin, D ;
Sitaraman, SV .
GASTROENTEROLOGY, 2005, 129 (06) :1991-2008
[3]   Biomarkers of Therapeutic Response in the IL-23 Pathway in Inflammatory Bowel Disease [J].
Cayatte, Corinne ;
Joyce-Shaikh, Barbara ;
Vega, Felix ;
Boniface, Katia ;
Grein, Jeffrey ;
Murphy, Erin ;
Blumenschein, Wendy M. ;
Chen, Smiley ;
Malinao, Maria-Christina ;
Basham, Beth ;
Pierce, Robert H. ;
Bowman, Edward P. ;
McKenzie, Brent S. ;
Elson, Charles O. ;
Faubion, William A. ;
Malefyt, Rene de Waal ;
Kastelein, Robert A. ;
Cua, Daniel ;
McClanahan, Terrill K. ;
Beaumont, Maribel .
CLINICAL AND TRANSLATIONAL GASTROENTEROLOGY, 2012, 3
[4]  
COOPER HS, 1993, LAB INVEST, V69, P238
[5]  
DOE WF, 1982, CLIN EXP IMMUNOL, V48, P256
[6]   Recent advances in MMP inhibitor design [J].
Fisher, JF ;
Mobashery, S .
CANCER AND METASTASIS REVIEWS, 2006, 25 (01) :115-136
[7]   A metalloproteinase inhibitor prevents lethal acute graft-versus-host disease in mice [J].
Hattori, K ;
Hirano, T ;
Ushiyama, C ;
Miyajima, H ;
Yamakawa, N ;
Ebata, T ;
Wada, Y ;
Ikeda, S ;
Yoshino, K ;
Tateno, M ;
Oshimi, K ;
Kayagaki, N ;
Yagita, H ;
Okumura, K .
BLOOD, 1997, 90 (02) :542-548
[8]   Recruitment of stem and progenitor cells from the bone marrow niche requires MMP-9 mediated release of Kit-ligand [J].
Heissig, B ;
Hattori, K ;
Dias, S ;
Friedrich, M ;
Ferris, B ;
Hackett, NR ;
Crystal, RG ;
Besmer, P ;
Lyden, D ;
Moore, MAS ;
Werb, Z ;
Rafii, S .
CELL, 2002, 109 (05) :625-637
[9]   The plasminogen fibrinolytic pathway is required for hematopoietic regeneration [J].
Heissig, Beate ;
Lund, Leif R. ;
Akiyama, Haruyo ;
Ohki, Makiko ;
Morita, Yohei ;
Romer, John ;
Nakauchi, Hiromitsu ;
Okumura, Ko ;
Ogawa, Hideoki ;
Werb, Zena ;
Dano, Keld ;
Hattori, Koichi .
CELL STEM CELL, 2007, 1 (06) :658-670
[10]   New functions of the fibrinolytic system in bone marrow cell-derived angiogenesis [J].
Heissig, Beate ;
Ohki-Koizumi, Makiko ;
Tashiro, Yoshihiko ;
Gritli, Ismael ;
Sato-Kusubata, Kaori ;
Hattori, Koichi .
INTERNATIONAL JOURNAL OF HEMATOLOGY, 2012, 95 (02) :131-137