• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Effectiveness of lentivirus-mediated RNA interference targeting mouse tumor necrosis factor α and .慢病毒介导的靶向小鼠肿瘤坏死因子α的RNA干扰的有效性及...... (原文此处不完整)
Exp Ther Med. 2018 Feb;15(2):2134-2139. doi: 10.3892/etm.2017.5609. Epub 2017 Dec 11.
2
Lentivirus-mediated short hairpin RNA interference targeting TNF-alpha in macrophages inhibits particle-induced inflammation and osteolysis in vitro and in vivo.慢病毒介导的巨噬细胞中靶向肿瘤坏死因子-α的短发夹RNA干扰在体内外均可抑制颗粒诱导的炎症和骨溶解。
BMC Musculoskelet Disord. 2016 Oct 18;17(1):431. doi: 10.1186/s12891-016-1290-6.
3
[Effects of exosomes from human adipose-derived mesenchymal stem cells on inflammatory response of mouse RAW264.7 cells and wound healing of full-thickness skin defects in mice].人脂肪间充质干细胞来源外泌体对小鼠RAW264.7细胞炎症反应及小鼠全层皮肤缺损创面愈合的影响
Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2022 Mar 20;38(3):215-226. doi: 10.3760/cma.j.cn501120-20201116-00477.
4
[Effects of Krüppel-like factor 4 on inflammatory response and organ injury in septic mice].[Krüppel样因子4对脓毒症小鼠炎症反应及器官损伤的影响]
Zhonghua Shao Shang Yu Chuang Mian Xiu Fu Za Zhi. 2022 Nov 20;38(11):1047-1056. doi: 10.3760/cma.j.cn501225-20220111-00005.
5
RNAi Silencing of IL-1β and TNF-α in the Treatment of Post-traumatic Arthritis in Rabbits.RNA干扰沉默白细胞介素-1β和肿瘤坏死因子-α在兔创伤后关节炎治疗中的应用
Chem Biol Drug Des. 2015 Dec;86(6):1466-70. doi: 10.1111/cbdd.12611. Epub 2015 Jul 20.
6
[Effect of Down-Regulating the CD59 by RNAi Lentivirus on the Expression of Acute T-lineage Leukemia Jurkat Cell Line].[RNA干扰慢病毒下调CD59对急性T淋巴细胞白血病Jurkat细胞系表达的影响]
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2019 Dec;27(6):1744-1748. doi: 10.19746/j.cnki.issn.1009-2137.2019.06.006.
7
Comparison of anti-rheumatic effects of local RNAi-based therapy in collagen induced arthritis rats using various cytokine genes as molecular targets.以多种细胞因子基因为分子靶点,比较基于RNA干扰的局部治疗对胶原诱导性关节炎大鼠的抗风湿效果。
Mod Rheumatol. 2009;19(2):125-33. doi: 10.1007/s10165-008-0131-3. Epub 2008 Nov 22.
8
Targeted knockout of TNF-α by injection of lentivirus-mediated siRNA into the subacromial bursa for the treatment of subacromial bursitis in rats.通过向大鼠肩峰下滑囊注射慢病毒介导的小干扰RNA靶向敲除肿瘤坏死因子-α用于治疗大鼠肩峰下滑囊炎
Mol Med Rep. 2015 Sep;12(3):4389-4395. doi: 10.3892/mmr.2015.3985. Epub 2015 Jun 23.
9
Anti-angiogenic effect of Shikonin in rheumatoid arthritis by downregulating PI3K/AKT and MAPKs signaling pathways.紫草素通过下调 PI3K/AKT 和 MAPKs 信号通路对类风湿关节炎的抗血管生成作用。
J Ethnopharmacol. 2020 Oct 5;260:113039. doi: 10.1016/j.jep.2020.113039. Epub 2020 Jun 1.
10
CXCR3 antagonist NBI-74330 mitigates joint inflammation in Collagen-Induced arthritis model in DBA/1J mice.CXCR3 拮抗剂 NBI-74330 可减轻 DBA/1J 小鼠胶原诱导性关节炎模型中的关节炎症。
Int Immunopharmacol. 2023 May;118:110099. doi: 10.1016/j.intimp.2023.110099. Epub 2023 Apr 3.

引用本文的文献

1
[Effects of lentivirus-mediated insulin-like growth factor 1 and platelet derived growth factor genes on nucleus pulposus tissue of human degenerated intervertebral disc].[慢病毒介导的胰岛素样生长因子1和血小板衍生生长因子基因对人退变椎间盘髓核组织的影响]
Zhongguo Xiu Fu Chong Jian Wai Ke Za Zhi. 2020 Jul 15;34(7):907-914. doi: 10.7507/1002-1892.201910101.

本文引用的文献

1
Construction and identification of an RNA interference lentiviral vector targeting the mouse TNF-α gene.靶向小鼠TNF-α基因的RNA干扰慢病毒载体的构建与鉴定
Exp Ther Med. 2015 Dec;10(6):2283-2288. doi: 10.3892/etm.2015.2813. Epub 2015 Oct 19.
2
Collagen-Induced Arthritis: A model for Murine Autoimmune Arthritis.胶原诱导性关节炎:一种小鼠自身免疫性关节炎模型。
Bio Protoc. 2015 Oct 20;5(20). doi: 10.21769/bioprotoc.1626.
3
Lentiviral transduction of neuronal cells.慢病毒介导的神经元细胞转导。
Methods Mol Biol. 2013;1078:141-6. doi: 10.1007/978-1-62703-640-5_12.
4
Lentiviral delivery of RNAi for in vivo lineage-specific modulation of gene expression in mouse lung macrophages.慢病毒介导的 RNAi 在体小鼠肺巨噬细胞中基因表达的谱系特异性调节。
Mol Ther. 2013 Apr;21(4):825-33. doi: 10.1038/mt.2013.19. Epub 2013 Feb 12.
5
Gene delivery to pancreatic exocrine cells in vivo and in vitro.体内和体外胰腺外分泌细胞的基因递送。
BMC Biotechnol. 2012 Oct 22;12:74. doi: 10.1186/1472-6750-12-74.
6
Targeting TNF receptors in rheumatoid arthritis.靶向治疗类风湿关节炎中的 TNF 受体。
Int Immunol. 2012 May;24(5):275-81. doi: 10.1093/intimm/dxs047. Epub 2012 Mar 28.
7
[Effects of RNAi on cyclooxygenase-2 expression and biologic activity of human rheumatoid arthritis synovial fibroblasts].RNA干扰对人类风湿关节炎滑膜成纤维细胞环氧化酶-2表达及生物学活性的影响
Zhonghua Yi Xue Za Zhi. 2007 Nov 6;87(41):2925-8.
8
Off-targeting and other non-specific effects of RNAi experiments in mammalian cells.RNA干扰实验在哺乳动物细胞中的脱靶效应及其他非特异性效应。
Curr Opin Mol Ther. 2007 Jun;9(3):248-57.
9
Off-target effects by siRNA can induce toxic phenotype.小干扰RNA的脱靶效应可诱导毒性表型。
RNA. 2006 Jul;12(7):1188-96. doi: 10.1261/rna.28106. Epub 2006 May 8.
10
3' UTR seed matches, but not overall identity, are associated with RNAi off-targets.3'非翻译区种子匹配而非整体一致性与RNA干扰脱靶效应相关。
Nat Methods. 2006 Mar;3(3):199-204. doi: 10.1038/nmeth854.

慢病毒介导的靶向小鼠肿瘤坏死因子α的RNA干扰的有效性及...... (原文此处不完整)

Effectiveness of lentivirus-mediated RNA interference targeting mouse tumor necrosis factor α and .

作者信息

Wang Jibo, Zhao Yingjie, Xin Miaomiao, Pan Lin, Wang Liqin, Yang Kun

机构信息

Department of Rheumatology and Clinical Immunology, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.

Department of Central Laboratory, The Affiliated Hospital of Qingdao University, Qingdao, Shandong 266003, P.R. China.

出版信息

Exp Ther Med. 2018 Feb;15(2):2134-2139. doi: 10.3892/etm.2017.5609. Epub 2017 Dec 11.

DOI:10.3892/etm.2017.5609
PMID:29434816
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5776641/
Abstract

The aim of the present study was to identify the effectiveness of lentivirus-mediated RNA interference (RNAi) targeting mouse tumor necrosis factor-α (TNF-α). RNAi lentivirus was used to transfect RAW264.7 cells, and the expression of -α, interleukin ()-β and mRNAs and TNF-α protein in RAW264.7 cells was measured by reverse transcription quantitative polymerase chain reaction (RT-qPCR) and enzyme-linked immunosorbent assay, respectively. , mice with collagen-induced arthritis (CIA) were injected intravenously with RNAi lentivirus, and CIA arthritis scores and the serum levels of TNF-α were detected. Additionally, joint tissues were subjected to pathological examination. In the cells, the expression level of -α mRNA in the RNAi lentivirus group was 0.29±0.02, which was significantly lower than that of the lentivirus negative control (0.93±0.01; t=25.4, P<0.001). In the mice, the serum TNF-α level in the RNAi lentivirus group was 249.25±11.22 ng/ml, which was significantly lower than that of the negative control group (381.86±6.28 ng/ml; P<0.05). However, no difference in α and mRNA levels was identified among the groups (t=1.00, P=0.37; t=1.22, P=0.29). The CIA arthritis score in the RNAi lentivirus group was significantly reduced compared with those in the control and negative control groups (P<0.05). Furthermore, the arthritis scores in the RNAi lentivirus and positive control groups continued to decrease for ≥2 weeks, and the serum TNF-α levels in the RNAi lentivirus and positive control groups were 31.58±2.18 and 35.21±2.25 pg/ml, which were significantly lower than those in the negative control group (46.62±3.02 pg/ml; P<0.05). Thus, targeting of the -α gene in mice via lentivirus-mediated RNAi and achieved TNF-α gene downregulation, which indicates that lentivirus-mediated RNA interference may be an effective form of gene therapy against rheumatoid arthritis.

摘要

本研究的目的是确定慢病毒介导的RNA干扰(RNAi)靶向小鼠肿瘤坏死因子-α(TNF-α)的有效性。使用RNAi慢病毒转染RAW264.7细胞,分别通过逆转录定量聚合酶链反应(RT-qPCR)和酶联免疫吸附测定法检测RAW264.7细胞中TNF-α、白细胞介素(IL)-β和mRNA的表达以及TNF-α蛋白。此外,将胶原诱导性关节炎(CIA)小鼠静脉注射RNAi慢病毒,检测CIA关节炎评分和TNF-α的血清水平。另外,对关节组织进行病理检查。在细胞中,RNAi慢病毒组中TNF-α mRNA的表达水平为0.29±0.02,显著低于慢病毒阴性对照组(0.93±0.01;t=25.4,P<0.001)。在小鼠中,RNAi慢病毒组的血清TNF-α水平为249.25±11.22 ng/ml,显著低于阴性对照组(381.86±6.28 ng/ml;P<0.05)。然而,各组之间α和mRNA水平未发现差异(t=1.00,P=0.37;t=1.22,P=0.29)。与对照组和阴性对照组相比,RNAi慢病毒组的CIA关节炎评分显著降低(P<0.05)。此外,RNAi慢病毒组和阳性对照组的关节炎评分持续下降≥2周,RNAi慢病毒组和阳性对照组的血清TNF-α水平分别为31.58±2.18和35.21±2.25 pg/ml,显著低于阴性对照组(46.62±3.02 pg/ml;P<0.05)。因此,通过慢病毒介导的RNAi靶向小鼠中的TNF-α基因可实现TNF-α基因下调,这表明慢病毒介导的RNA干扰可能是一种针对类风湿性关节炎的有效基因治疗形式。