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B7-H4在实验性自身免疫性心肌炎小鼠中的表达 被引量:1

Expression of B7-H4 in experimental autoimmune myocarditis
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摘要 目的:研究新型共刺激分子B7-H4在实验性自身免疫性心肌炎小鼠发病中表达情况。方法:将BALB/c小鼠随机分为对照组与实验组。给实验组小鼠注射猪心肌肌凝蛋白建立实验性自身免疫性心肌炎模型,对照组给予同体积不含肌凝蛋白的完全弗氏佐剂及生理盐水。在实验的第14、21、30、45天分批处死小鼠,提取组织进行淋巴细胞增殖实验、苏木素-伊红(HE)染色、免疫组织化学染色及实时荧光定量PCR(real-time PCR)。结果:心肌炎症改变在第21、30天时最严重,之后逐渐降低;淋巴细胞增殖实验与real-time PCR的结果与心肌炎症情况类似,在实验期间随炎症情况变化,较正常均增高(P<0.05);免疫组化结果显示B7-H4蛋白在心肌炎的心肌血管内皮恒定表达。结论:新型共刺激分子B7-H4参与心肌炎病程,可能为心肌炎的发病机制提供新的研究思路。 Objective:To observe the expression of B7-H4 in experimental autoimmune myocarditis (EAM).Methods:BALB/c mice were randomly divided into 2 groups:the control group and the experimental group.The mice of experimental group were injected with myosin to establish EAM models , while the mice of control group were injected with complete Freund 's adjuvant and normal saline.All the mice were killed separately at the 14th,21st,30th and 45th day for lymphocyte proliferation assay ,hematoxylin-eosin staining,immunohistochemical staining and real-time PCR.Results:The inflammation infiltration of heart was most serious at the 14th and 21st day,then it was gradually relieved with time;the results of lymphocyte proliferation assay and real-time PCR were similar to that of the inflammation infiltration of heart ,which were in high level at the 14th and 21st day,and they were both higher than that of the control group ( P〈0.05 );B7-H4 protein were only detected in the experimental group ,and it was constantly expressed during the whole experiment on the endothelium of heart with myocarditis.Conclusion:B7-H4 participates in the progress of EAM ,and it may be a new way of studying the mechanism of myocarditis.
出处 《中国免疫学杂志》 CAS CSCD 北大核心 2014年第6期745-748,753,共5页 Chinese Journal of Immunology
基金 国家自然科学基金项目(81070188)资助
关键词 B7一H4 共刺激分子 实验性自身免疫性心肌炎 B7-H4 Costimulatory molecules Experimental autoimmune myocarditis
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  • 1Senger DR, Wirth DF, Hynes RO. Transformed mammalian cells secrete specific proteins and phosphoproteins [J]. Cell, 1979,16(4) : 885-893.
  • 2Bao LH, Sakaguchi H, Fujimoto J, et al. Osteopontin in metastatic lesions as a prognostic marker in ovarian cancers [J].J Biomed Sci, 2007,14(3):373-381.
  • 3Rosen DG, Wang L, Atkinson JN, et al. Potential markers that complement expression of CA125 in epithelial ovarian cancer[J].Gynecol Oncol, 2005,99 (2) : 267-277.
  • 4Kim JH, Skates SJ, Uede T, et al. Osteopontin as a potential diagnostic biomarker for ovarian cancer [J]. JAMA, 2002,287 (13) : 1671-1679.
  • 5Coppola D, Szabo M, Boulware D, et al. Correlation of osteopontin protein expression and pathological stage across a wide variety of tumor histologies [J]. Clin Cancer Res, 2004, 10( 1 ) : 184-190.
  • 6Denhardt DT, Mistretta D, Chambers AF, et al. Transcriptional regulation of osteopontin and the metastatic phenotype:evidence for a ras-activated enhancer in the human open promoter [ J ]. Clin Exp Metastasis, 2003,20 ( 1 ) : 77-84.
  • 7Ito T, Hashimoto Y, Tanaka E, et al. An inducible shorthairpin RNA vector against osteopontin reduces metastatic potential of human esophageal squamous cell carcinoma in vitro and in vivo [J]. Clin Cancer Res, 2006, 12 (4) : 1308-1316.
  • 8Sica GL, Choi IH, Zhu G, et al. B7-H4, a molecule of the B7 family, negatively regulates T cell immunity [J]. Immunity, 2003,18(6) : 849-861.
  • 9Sica GL, Choi IH, Zhu G, et al. B7-H4, a molecule of the B7 family, negatively regulates T cell immunity [J]. Immunity, 2003,18(6) : 849-861.
  • 10Choi ZH, Zhu GL, Sica GL, et al. Genomic organization and expression analysis of B7-H4, an immune inhibitory molecule of the B7 family [J]. Immunol, 2003,171(9) :4650-4654.

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