首页 | 本学科首页   官方微博 | 高级检索  
     

构建双基因共表达腺病毒载体转染关节炎模型大鼠的意义
引用本文:樊 萍,何 岚,郝志明,蒲 丹,吕晓虹,孙怡宁,胡 楠,王研华,丁小明,李 杨,薛武军. 构建双基因共表达腺病毒载体转染关节炎模型大鼠的意义[J]. 中国组织工程研究, 2015, 19(18): 2825-2830. DOI: 10.3969/j.issn.2095-4344.2015.18.007
作者姓名:樊 萍  何 岚  郝志明  蒲 丹  吕晓虹  孙怡宁  胡 楠  王研华  丁小明  李 杨  薛武军
作者单位:西安交通大学医学院第一附属医院,1风湿免疫科,2肾移植科,陕西省西安市 710061
基金项目:国家自然科学基金项目资助(81400677);陕西省科学技术研究发展计划项目资助(2012K16-09-02)
摘    要:
背景:淋巴细胞异常激活以及核因子κB依赖非特异性的炎症反应是类风湿关节炎关节组织炎症损害的两个重要方面。共刺激信号CD40/CD40L是T细胞识别、活化中最重要的共刺激分子。IκBα有效的抑制核因子κB的途径,可以在中心环节上抑制炎症反应的产生,抑制炎症因子滑膜组织的损害。目的:采用CD40LIg-IRES2-IκBα双基因表达的腺病毒载体转染到关节炎动物模型,探索双基因共表达腺病毒载体转染对免疫性关节炎的治疗效果。方法:构建pAdCD40LIg-IRES2-IκBα双基因共表达腺病毒载体。采用含1 g/L Ⅱ型胶原蛋的完全弗氏佐剂皮下多点注射构建关节炎Wistar大鼠模型。将20只构建成功的关节炎大鼠模型分为未处理组和转染组,分别给予2组大鼠四肢末端关节腔注射生理盐水和pAdCD40LIg-IRES2-IκBα腺病毒载体。结果与结论:转染14 d后,与未处理组相比,转染组大鼠关节炎评分、关节液中淋巴细胞CD40L表达水平、关节滑膜组织中核因子κB p65表达水平、关节液内白细胞介素2、白细胞介素6、肿瘤坏死因子α、间质金属蛋白酶3和间质金属蛋白酶9的水平降低。提示共表达CD40LIg和IκBα腺病毒载体局部转染可有效抑制关节炎大鼠关节炎症状,降低关节腔内炎性细胞因子及炎性分子在滑膜组织中的表达,取得良好的治疗效果。中国组织工程研究杂志出版内容重点:肾移植;肝移植;移植;心脏移植;组织移植;皮肤移植;皮瓣移植;血管移植;器官移植;组织工程全文链接:

关 键 词:实验动物  骨及关节损伤模型  关节炎  类风湿  CD40L  IκBα  核因子κB  共刺激信号  炎症  滑膜  国家自然科学基金  
收稿时间:2015-03-12

Transfection of double gene co-expressing adenovirus vector into arthritis rats
Fan Ping,He Lan,Hao Zhi-ming,Pu Dan,Lv Xiao-hong,Sun Yi-ning,Hu Nan,Wang Yan-hua,Ding Xiao-ming,Li Yang,Xue Wu-jun. Transfection of double gene co-expressing adenovirus vector into arthritis rats[J]. Chinese Journal of Tissue Engineering Research, 2015, 19(18): 2825-2830. DOI: 10.3969/j.issn.2095-4344.2015.18.007
Authors:Fan Ping  He Lan  Hao Zhi-ming  Pu Dan  Lv Xiao-hong  Sun Yi-ning  Hu Nan  Wang Yan-hua  Ding Xiao-ming  Li Yang  Xue Wu-jun
Affiliation:1Department of Rheumatism, 2Department of Renal Transplantation, First Affiliated Hospital of Xi’an Jiaotong University Health Science Center, Xi’an 710061, Shaanxi Province, China
Abstract:
BACKGROUND: Abnormal activation of lymphocytes and nuclear factor κB-dependent non-specific inflammation are two major manifestations of joint damage in rheumatoid arthritis. Co-stimulatory signal CD40/CD40L is the dominant co-stimulatory factor in the recognition and activation of T cells. IκBα effectively inhibits nuclear factor κB pathway, prevent the inflammation in the central link, and suppress the damage caused by inflammatory factor in the synovial tissue.OBJECTIVE: To investigate the therapeutic effect of double gene co-expressing adenovirus vector on arthritis based on an arthritis model rat transfected by CD40LIg-IRES2-IκBα co-expressing adenovirus vector.METHODS: The pAdCD40LIg-IRES2-IκBα co-expressing adenovirus vector was established. Arthritic model was established through multi-subcutaneous injections of complete Freund's adjuvant of type collagen II (1 g/L) into Wistar rats. Then 20 arthritic rats were divided into two groups: untreated group and transfection group, receiving an injection of saline and pAdCD40LIg-IRES2-IκBα adenovirus vector to distal joint cavity of limbs, respectively. RESULTS AND CONCLUSION: At 14 days post-transfection, compared with the untreated group, the mean arthritis index score, the CD40L expression of lymphocytes in synovial fluid, the nuclear factor-κB p65 expression in synovial tissue, and levels of interleukin-2, interleukin-6, tumor necrosis factor-α, matrix metalloproteinase-3 and matrix metalloproteinase-9 in synovial fluid of rats in transfection group were significantly lower than those in   untreated group. Focal transfection of the CD40LIg-IκBα co-expression adenovirus vector can effectively inhibit arthritic symptoms, and reduce the expressions of inflammatory cytokine in synovial fluid and inflammatory molecule in synovial tissue of arthritic rats, which shows good therapeutic effect.
Keywords:Arthritis  Adenoviridae Infections  Lymphocytes  T-Lymphocytes  
本文献已被 CNKI 等数据库收录!
点击此处可从《中国组织工程研究》浏览原始摘要信息
点击此处可从《中国组织工程研究》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号