Possible Involvement of Foxp3(+) Regulatory T Cells in the Development of Immune-Mediated Pancreatitis in MRL/Mp Mice Treated with Polyinosinic: Polycytidylic Acid

被引:4
|
作者
Koyabu, Masanori [1 ]
Uchida, Kazushige [1 ]
Sakaguchi, Yutaku [1 ]
Fukata, Norimasa [1 ]
Kusuda, Takeo [1 ]
Miyoshi, Hideaki [1 ]
Yoshida, Katsunori [1 ]
Sumimoto, Kimi [1 ]
Mitsuyama, Toshiyuki [1 ]
Fukui, Toshiro [1 ]
Nishio, Akiyoshi [1 ]
Okazaki, Kazuichi [1 ]
机构
[1] Kansai Med Univ, Dept Internal Med 3, Div Gastroenterol & Hepatol, 10-15 Fumizono, Moriguchi, Osaka 5708507, Japan
关键词
D O I
10.1155/2013/367325
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives. This study was conducted to clarify whether or not Tregs are involved in the development of immune-mediated pancreatitis in MRL/Mp mice as an AIP (autoimmune pancreatitis) model, in order to understand more clearly the pathogenic mechanism of AIP. Methods. We compared the immunohistochemical features of pancreatic forkhead box P3 (Foxp3) in the administration of poly I: C in MRL/Mp mice and two types of control mice (BALB/c and C57BL/6). As a contrast, we analyzed three mouse models of pancreatitis without autoimmune mechanism (Cerulein-, Ligation-, and Ligation + Cerulein-treated mice). After staining these specimens, we compared the ratios of Foxp3-positive cells to infiltrated mononuclear cells (Foxp3/Mono). Results. Our immunohistochemical study of Foxp3 revealed that the infiltration of Foxp3-positive cells increased in poly I: C-treated MRL/Mp mice. The histopathological score of pancreatitis showed no difference among poly I: C-treated MRL/Mp, Ligation-, and Ligation + Cerulein-treated mice; however, the Foxp3/Mono ratio in poly I: C-treated MRL/Mp mice was significantly increased compared with Ligation-and Ligation + Cerulein-treated mice. Conclusions. MRL/Mp mice treated with poly I: C showed early development of pancreatitis with abundant infiltration of Foxp3-positive cells. There may be a possibility that Tregs are involved in the development of pancreatitis in these mice.
引用
收藏
页数:10
相关论文
共 14 条
  • [1] Depletion of Foxp3(+) regulatory T cells augments CD4(+) T cell immune responses in atherosclerosis-prone hypercholesterolemic mice
    Kasahara, Kazuyuki
    Sasaki, Naoto
    Amin, Hilman Zulkifli
    Tanaka, Toru
    Horibe, Sayo
    Yamashita, Tomoya
    Hirata, Ken-Ichi
    Rikitake, Yoshiyuki
    HELIYON, 2022, 8 (08)
  • [2] Combined insulin B:9-23 self-peptide and polyinosinic-polycytidylic acid accelerate insulitis but inhibit development of diabetes by increasing the proportion of CD4+Foxp3+ regulatory T cells in the islets in nonobese diabetic mice
    Fukushima, K.
    Abiru, N.
    Nagayama, Y.
    Satoh, T.
    Nakahara, M.
    Kawasaki, E.
    Yamasaki, H.
    Eguchi, K.
    ACTA DIABETOLOGICA, 2007, 44 : S16 - S16
  • [3] INCREASED LEVEL OF CD4+CD25+FOXP3+REGULATORY T CELLS IN THE PERIPHERAL BLOOD OF 7 DOGS WITH IMMUNE-MEDIATED HEMOLYTIC ANEMIA
    Baek, Dae-seung
    Lee, Hyunseok
    Kim, Yun-hye
    Song, Ruhui
    Park, Jinho
    Park, Chul
    JOURNAL OF VETERINARY INTERNAL MEDICINE, 2013, 27 (03) : 719 - 719
  • [4] Lineage-Plasticity and Inflammatory Change of Human FoxP3+ Regulatory T Cells in Acute Viral Infection: Implication in Immune-Mediated Tissue Injury
    Choi, Yoon Seok
    Lee, Jeewon
    Song, Ik-Chan
    Jo, Deog-Yeon
    Shin, Eui-Cheol
    BLOOD, 2014, 124 (21)
  • [5] Combined insulin B:9-23 self-peptide and polyinosinic-polycytidylic acid accelerate insulitis but inhibit development of diabetes by increasing the proportion of CD4+Foxp3+ regulatory T cells in the islets in non-obese diabetic mice
    Fukushima, Keiko
    Abiru, Norio
    Nagayama, Yuji
    Kobayashi, Masakazu
    Satoh, Tsuyoshi
    Nakahara, Mami
    Kawasaki, Eiji
    Yamasaki, Hironori
    Ueha, Satoshi
    Matsushima, Koji
    Liu, Edwin
    Eguchi, Katsumi
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 367 (04) : 719 - 724
  • [6] In Vitro Expanded CD4+CD25+Foxp3+ Regulatory T Cells Maintain a Normal Phenotype and Suppress Immune-Mediated Ocular Surface Inflammation
    Siemasko, Karyn F.
    Gao, Jianping
    Calder, Virginia L.
    Hanna, Rebecca
    Calonge, Margarita
    Pflugfelder, Stephen C.
    Niederkorn, Jerry Y.
    Stern, Michael E.
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2008, 49 (12) : 5434 - 5440
  • [7] Contrasting roles for all-trans retinoic acid in TGF-β-mediated induction of Foxp3 and Il10 genes in developing regulatory T cells
    Maynard, Craig L.
    Hatton, Robin D.
    Helms, Whitney S.
    Oliver, James R.
    Stephensen, Charles B.
    Weaver, Casey T.
    JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (02): : 343 - 357
  • [8] CD4+FOXP3+ regulatory T cells confer long-term regulation of factor VIII-specific immune responses in plasmid-mediated gene therapy-treated hemophilia mice
    Miao, Carol H.
    Harmeling, Benjamin R.
    Ziegler, Steven F.
    Yen, Benjamin C.
    Torgerson, Troy
    Chen, Liping
    Yau, Roger J.
    Peng, Baowei
    Thompson, Arthur R.
    Ochs, Hans D.
    Rawlings, David J.
    BLOOD, 2009, 114 (19) : 4034 - 4044
  • [9] Foxp3+CD25+ T regulatory cells stimulate IFN-γ-Independent CD152-mediated activation of tryptophan catabolism that provides dendritic cells with immune regulatory activity in mice unresponsive to staphylococcal enterotoxin B
    Feunou, Pascal
    Vanwetswinkel, Sophie
    Gaudray, Florence
    Goldman, Michel
    Matthys, Patrick
    Braun, Michel Y.
    JOURNAL OF IMMUNOLOGY, 2007, 179 (02): : 910 - 917
  • [10] Involvement of Foxp3-expressing CD4+ CD25+ regulatory T cells in the development of tolerance induced by transforming growth factor-β2-treated antigen-presenting cells
    Zhang, Haining
    Yang, Peizeng
    Zhou, Hongyan
    Meng, Qianli
    Huang, Xiangkun
    IMMUNOLOGY, 2008, 124 (03) : 304 - 314