中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

辅助性T淋巴细胞22及其效应因子IL-22在自身免疫性肝炎小鼠模型中的表达及意义

潘景 潘文婷 吴丽慧

引用本文:
Citation:

辅助性T淋巴细胞22及其效应因子IL-22在自身免疫性肝炎小鼠模型中的表达及意义

DOI: 10.3969/j.issn.1001-5256.2018.08.030
基金项目: 

国家自然科学基金(H0923;H0929); 

详细信息
  • 中图分类号: R-332;R575.1

Expression and significance of Th22 cells and its functional factor interleukin-22 in mice with autoimmune hepatitis

Research funding: 

 

  • 摘要:

    目的研究自身免疫性肝炎(AIH)小鼠模型中辅助性T淋巴细胞(Th)22细胞水平及其功能因子IL-22的表达情况,探索其在AIH发病中的意义。方法选取30只4周龄雄性C57BL/6小鼠随机分为对照组(n=6)、AIH组(n=14),剩余10只用于提取肝脏特异性抗原S100。在实验第1天和第7天通过腹腔注射法将新鲜提取的S100与等体积弗氏完全佐剂混合液注射到小鼠腹腔内,第28天成功建立AIH小鼠模型(造模期间AIH组有7只小鼠因注射不当、出现腹水、感染等原因死亡)后,将小鼠经腹腔注射5%水合氯醛(0.1 ml/10 g)麻醉后摘取眼球取血,收集小鼠脾脏采用流式细胞术检测Th22细胞数,RT-PCR检测AHR mRNA水平;收集肝组织用于HE染色观察肝脏病理变化,RT-PCR和免疫印迹法检测肝组织IL-22、IL-22R表达情况;ELISA法检测血清中IL-22细胞因子水平。2组间比较采用t检验。结果对照组小鼠肝组织排列整齐,肝小叶结构清晰,AIH组小鼠汇管区有大量炎症细胞浸润,肝组织出现点状甚至碎片状坏死。AIH组Th22细胞数较对照组明显升高[(0.083±0.052)%vs(1.55...

     

  • [1]MAKOL A, WATT KD, CHOWDHARY VR.Autoimmune hepatitis:A review of current diagnosis and treatment[J].Hepat Res Treat, 2011, 2011:390916.
    [2]HENEGHAN MA, YEOMAN AD, VERMA S, et al.Autoimmune hepatitis[J].J Lancet, 2013, 382 (9902) :1433-1444.
    [3]CZAJA AJ.Autoimmune hepatitis in diverse ethnic populations and geographical regions[J].Expert Rev Gastroenterol Hepatol, 2013, 7 (4) :365-385.
    [4]ABDOLLAHI MR, SOMI MH, FARAJI E.Role of international criteria in the diagnosis of autoimmune hepatitis[J].World J Gastroenterol, 2013, 19 (23) :3629-3633.
    [5]MANNS MP, LOHSE AW, VERGANI D.Autoimmune hepatitis——Update 2015[J].J Hepatol, 2015, 62 (1 Suppl) :s100-s111.
    [6]HONDA K.IL-22 from T cells:Better late than never[J].Immunity, 2012, 37 (6) :952-954.
    [7]ROLLA S, BARDINA V, de MERCANTI S, et al.Th22 cells are expanded in multiple sclerosis and are resistant to IFN-beta[J].J Leukoc Biol, 2014, 96 (6) :1155-1164.
    [8]BENHAM H, NORRIS P, GOODALL J, et al.Th17 and Th22cells in psoriatic arthritis and psoriasis[J].Arthritis Res Ther, 2013, 15 (5) :r136.
    [9]LUAN L, DING Y, HAN S, et al.An increased proportion of circulating Th22 and Tc22 cells in psoriasis[J].Cell Immunol, 2014, 290 (2) :196-200.
    [10]SONNENBERG GF, FOUSER LA, ARTIS D.Functional biology of the IL-22-IL-22R pathway in regulating immunity and inflammation at barrier surfaces[J].Adv Immunol, 2010, 107:1-29.
    [11]YANG X, ZHENG SG.Interleukin-22:A likely target for treatment of autoimmune diseases[J].Autoimmun Rev, 2014, 13 (6) :615-620.
    [12]LONGHI MS, MA Y, MIELI-VERGANI G, et al.Aetiopathogenesis of autoimmunehepatitis[J].J Autoimmun, 2010, 34 (1) :7-14.
    [13]LIBERAL R, GRANT CR, LONGHI MS, et al.Regulatory T cells:Mechanisms of suppression and impairment in autoimmune liver disease[J].Iubmb Life, 2015, 67 (2) :88-97.
    [14]SEBODE M, LOHSE AW.Future perspective:Immunomodulatory therapy for autoimmune hepatitis[J].Dig Dis, 2014, 32 (5) :502-506.
    [15]ZHANG L, LI YG, LI YH, et al.Increased frequencies of Th22 cells as well as Th17 cells in the peripheral blood of patients with ankylosing spondylitis and rheumatoid arthritis[J].Plos One, 2012, 7 (4) :e31000.
    [16]KAGAMI S, RIZZO HL, LEE JJ, et al.Circulating Th17, Th22, and Th1 cells are increased in psoriasis[J].J Invest Dermatol, 2010, 130 (5) :1373-1383.
    [17]ZHAO L, JIANG ZY, JIANG YF, et al.IL-22 (+) CD4 (+) T-cells in patients with active systemic lupus erythematosus[J].Exp Biol M, 2013, 238 (2) :193-199.
    [18]KAWATA K, TSUDA M, YANG GX, et al.Identification of potential cytokine pathways for therapeutic intervention in murine primary biliary cirrhosis[J].PLo S One, 2013, 8 (9) :e74225.
  • 加载中
计量
  • 文章访问数:  1913
  • HTML全文浏览量:  33
  • PDF下载量:  393
  • 被引次数: 0
出版历程
  • 收稿日期:  2018-03-03
  • 出版日期:  2018-08-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回