• 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

基质细胞衍生因子-1 调节滑膜炎症大鼠颞下颌关节中白细胞介素-1β的分泌。

Stromal cell-derived factor-1 regulates the secretion of interleukin-1β in the temporomandibular joint of rats with synovial inflammation.

机构信息

Department of Prosthodontics, Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, Shandong University Stomatology Hospital, Jinan, China.

Department of Prosthodontics, Jinan Stomatological Hospital, Jinan, China.

出版信息

J Oral Pathol Med. 2020 Oct;49(9):933-939. doi: 10.1111/jop.13040. Epub 2020 Jun 13.

DOI:10.1111/jop.13040
PMID:32449535
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7586974/
Abstract

BACKGROUND

Synovitis is characterized by the infiltration of inflammatory cells and often accompanies the pathological progression of the clinical symptoms affecting the temporomandibular joint (TMJ), such as pain, snapping, and limited mouth opening. It has been suggested that the signal transduction pathway and resultant proinflammatory mediators play important roles in the pathogenesis of synovitis. Therefore, in this present research, we aimed to investigate the changes in the expressions of stromal cell-derived factor 1 (SDF-1) and interleukin (IL)-1β in rats with occlusal interference.

MATERIALS AND METHODS

We divided 36 male Wistar rats into the following groups: Group A (control group), Group B (occlusal interference group), and Group C (AMD3100 group). Synovial inflammation was induced in the rats in Groups B and C to establish the occlusal interference model. The inflammatory changes were detected, and the expressions of SDF-1 and IL-1β in the synovium were assayed via immunostaining and a real-time quantitative polymerase chain reaction (PCR).

RESULTS

In Group B, obvious inflammatory changes were observed in the synovial membranes; additionally, the SDF-1 and IL-1β expression levels were significantly higher at the protein and mRNA levels. However, in Group C, these experimental results were inhibited by an injection with AMD3100.

CONCLUSION

These results may indicate that SDF-1 regulates the expression level of inflammatory factors, such as IL-1β, in the synovial membranes of rats with occlusal interference. Our findings suggest that the SDF-1 axis may contribute to the onset of synovitis during the development of TMJ joint disease.

摘要

背景

滑膜炎的特征是炎症细胞浸润,常伴有影响颞下颌关节(TMJ)的临床症状的病理进展,如疼痛、弹响和开口受限。有研究表明,信号转导通路和由此产生的促炎介质在滑膜炎的发病机制中起重要作用。因此,在本研究中,我们旨在研究咬合干扰大鼠基质细胞衍生因子 1(SDF-1)和白细胞介素(IL)-1β表达的变化。

材料和方法

将 36 只雄性 Wistar 大鼠分为以下三组:A 组(对照组)、B 组(咬合干扰组)和 C 组(AMD3100 组)。在 B 组和 C 组大鼠中建立咬合干扰模型,诱导滑膜炎症,通过免疫染色和实时定量聚合酶链反应(PCR)检测滑膜炎症的变化,并检测 SDF-1 和 IL-1β在滑膜中的表达。

结果

在 B 组中,滑膜膜明显出现炎症变化;此外,SDF-1 和 IL-1β 的蛋白和 mRNA 水平表达显著升高。然而,在 C 组中,AMD3100 的注射抑制了这些实验结果。

结论

这些结果可能表明 SDF-1 调节了咬合干扰大鼠滑膜中炎症因子如 IL-1β 的表达水平。我们的发现表明,SDF-1 轴可能参与了 TMJ 关节疾病发展过程中滑膜炎的发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/af1ba34ceb48/JOP-49-933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/6ebe53bf6fec/JOP-49-933-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/536a18c03c94/JOP-49-933-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/af1ba34ceb48/JOP-49-933-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/6ebe53bf6fec/JOP-49-933-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/536a18c03c94/JOP-49-933-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3346/7586974/af1ba34ceb48/JOP-49-933-g003.jpg

相似文献

1
Stromal cell-derived factor-1 regulates the secretion of interleukin-1β in the temporomandibular joint of rats with synovial inflammation.基质细胞衍生因子-1 调节滑膜炎症大鼠颞下颌关节中白细胞介素-1β的分泌。
J Oral Pathol Med. 2020 Oct;49(9):933-939. doi: 10.1111/jop.13040. Epub 2020 Jun 13.
2
Effect of Toll-Like Receptor 4 on Synovial Injury of Temporomandibular Joint in Rats Caused by Occlusal Interference.Toll样受体4对大鼠咬合干扰所致颞下颌关节滑膜损伤的影响
Mediators Inflamm. 2016;2016:7694921. doi: 10.1155/2016/7694921. Epub 2016 Jun 20.
3
Toll-Like Receptor 4 (TLR4) Stimulates Synovial Injury of Temporomandibular Joint in Rats Through the Activation of p38 Mitogen-Activated Protein Kinase (MAPK) Signaling Pathway.Toll 样受体 4(TLR4)通过激活丝裂原活化蛋白激酶(MAPK)信号通路刺激大鼠颞下颌关节滑膜损伤。
Med Sci Monit. 2018 Jun 26;24:4405-4412. doi: 10.12659/MSM.908526.
4
Tumor necrosis factor-alpha increases chemokine gene expression and production in synovial fibroblasts from human temporomandibular joint.肿瘤坏死因子-α增加人颞下颌关节滑膜成纤维细胞中趋化因子基因的表达及产生。
J Oral Pathol Med. 2005 Jul;34(6):357-63. doi: 10.1111/j.1600-0714.2005.00302.x.
5
Expression of cyclooxygenase-1 and -2 in IL-1beta-induced synovitis of the temporomandibular joint.环氧合酶-1 和 -2 在白介素-1β诱导的颞下颌关节炎性滑膜中的表达。
J Oral Pathol Med. 2009 Aug;38(7):584-90. doi: 10.1111/j.1600-0714.2008.00733.x. Epub 2008 Dec 30.
6
MicroRNA-381 Favors Repair of Nerve Injury Through Regulation of the SDF-1/CXCR4 Signaling Pathway via LRRC4 in Acute Cerebral Ischemia after Cerebral Lymphatic Blockage.微小RNA-381通过脑淋巴阻塞后急性脑缺血中LRRC4调控SDF-1/CXCR4信号通路促进神经损伤修复。
Cell Physiol Biochem. 2018;46(3):890-906. doi: 10.1159/000488821. Epub 2018 Apr 13.
7
Effect of interleukin-1beta and dehydroepiandrosterone on the expression of lumican and fibromodulin in fibroblast-like synovial cells of the human temporomandibular joint.白细胞介素-1β和脱氢表雄酮对人颞下颌关节成纤维样滑膜细胞中核心蛋白聚糖和纤调蛋白表达的影响
Eur J Histochem. 2015 Feb 23;59(1):2440. doi: 10.4081/ejh.2015.2440.
8
Effect of p38 Mitogen Activated Protein Kinase Inhibitor on Temporomandibular Joint Synovitis Induced by Occlusal Alteration.p38丝裂原活化蛋白激酶抑制剂对咬合改变所致颞下颌关节滑膜炎的影响
J Oral Maxillofac Surg. 2016 Jun;74(6):1131-9. doi: 10.1016/j.joms.2015.12.020. Epub 2016 Jan 7.
9
AMD3100 Attenuates Matrix Metalloprotease-3 and -9 Expressions and Prevents Cartilage Degradation in a Monosodium Iodo-Acetate-Induced Rat Model of Temporomandibular Osteoarthritis.AMD3100减轻碘乙酸钠诱导的大鼠颞下颌骨关节炎模型中基质金属蛋白酶-3和-9的表达并预防软骨降解。
J Oral Maxillofac Surg. 2016 May;74(5):927.e1-927.e13. doi: 10.1016/j.joms.2015.12.018. Epub 2016 Jan 7.
10
Inflammation and Temporomandibular Joint Derangement.炎症与颞下颌关节紊乱
Biol Pharm Bull. 2019;42(4):538-542. doi: 10.1248/bpb.b18-00442.

引用本文的文献

1
IL-37 counteracts inflammatory injury in the temporomandibular joint via the intracellular pathway.白细胞介素-37通过细胞内途径对抗颞下颌关节的炎性损伤。
Front Pharmacol. 2023 Nov 20;14:1250216. doi: 10.3389/fphar.2023.1250216. eCollection 2023.
2
Potential pathological and molecular mechanisms of temporomandibular joint osteoarthritis.颞下颌关节骨关节炎的潜在病理及分子机制
J Dent Sci. 2023 Jul;18(3):959-971. doi: 10.1016/j.jds.2023.04.002. Epub 2023 Apr 18.
3
Painful Temporomandibular Joint Clicking: Genetic Point of View.

本文引用的文献

1
Inflammation and Temporomandibular Joint Derangement.炎症与颞下颌关节紊乱
Biol Pharm Bull. 2019;42(4):538-542. doi: 10.1248/bpb.b18-00442.
2
SDF1/CXCR7 Signaling Axis Participates in Angiogenesis in Degenerated Discs via the PI3K/AKT Pathway.SDF1/CXCR7 信号轴通过 PI3K/AKT 通路参与退变椎间盘的血管生成。
DNA Cell Biol. 2019 May;38(5):457-467. doi: 10.1089/dna.2018.4531. Epub 2019 Mar 13.
3
Effects of altered CXCL12/CXCR4 axis on BMP2/Smad/Runx2/Osterix axis and osteogenic gene expressions during osteogenic differentiation of MSCs.
颞下颌关节弹响疼痛的遗传学观点
J Oral Facial Pain Headache. 2022 Summer;36(3-4):229–235. doi: 10.11607/ofph.3115. Epub 2022 Nov 28.
间充质干细胞成骨分化过程中CXCL12/CXCR4轴改变对BMP2/Smad/Runx2/osterix轴及成骨基因表达的影响。
Am J Transl Res. 2017 Apr 15;9(4):1680-1693. eCollection 2017.
4
Synovitis in osteoarthritis: current understanding with therapeutic implications.骨关节炎中的滑膜炎:当前认识及治疗意义
Arthritis Res Ther. 2017 Feb 2;19(1):18. doi: 10.1186/s13075-017-1229-9.
5
Modulation of stromal cell-derived factor 1 alpha (SDF-1α) and its receptor CXCR4 in Porphyromonas gingivalis-induced periodontal inflammation.牙龈卟啉单胞菌诱导的牙周炎症中基质细胞衍生因子1α(SDF-1α)及其受体CXCR4的调节
BMC Oral Health. 2016 Jul 22;17(1):26. doi: 10.1186/s12903-016-0250-8.
6
Effect of Toll-Like Receptor 4 on Synovial Injury of Temporomandibular Joint in Rats Caused by Occlusal Interference.Toll样受体4对大鼠咬合干扰所致颞下颌关节滑膜损伤的影响
Mediators Inflamm. 2016;2016:7694921. doi: 10.1155/2016/7694921. Epub 2016 Jun 20.
7
Blockade of hypoxia-induced CXCR4 with AMD3100 inhibits production of OA-associated catabolic mediators IL-1β and MMP-13.用AMD3100阻断缺氧诱导的CXCR4可抑制骨关节炎相关分解代谢介质白细胞介素-1β和基质金属蛋白酶-13的产生。
Mol Med Rep. 2016 Aug;14(2):1475-82. doi: 10.3892/mmr.2016.5419. Epub 2016 Jun 21.
8
AMD3100 Attenuates Matrix Metalloprotease-3 and -9 Expressions and Prevents Cartilage Degradation in a Monosodium Iodo-Acetate-Induced Rat Model of Temporomandibular Osteoarthritis.AMD3100减轻碘乙酸钠诱导的大鼠颞下颌骨关节炎模型中基质金属蛋白酶-3和-9的表达并预防软骨降解。
J Oral Maxillofac Surg. 2016 May;74(5):927.e1-927.e13. doi: 10.1016/j.joms.2015.12.018. Epub 2016 Jan 7.
9
Association of Joint Inflammation With Pain Sensitization in Knee Osteoarthritis: The Multicenter Osteoarthritis Study.关节炎炎症与膝关节骨关节炎疼痛敏化的相关性:多中心骨关节炎研究。
Arthritis Rheumatol. 2016 Mar;68(3):654-61. doi: 10.1002/art.39488.
10
Sclareol exerts anti-osteoarthritic activities in interleukin-1β-induced rabbit chondrocytes and a rabbit osteoarthritis model.硬尾醇对白细胞介素-1β诱导的兔软骨细胞和兔骨关节炎模型具有抗骨关节炎活性。
Int J Clin Exp Pathol. 2015 Mar 1;8(3):2365-74. eCollection 2015.