NELL1 Growth Factor Suppresses the NF-KB Signaling Pathway During Orthodontic Tooth Movement and Attenuates the Inflammatory Response

被引:0
|
作者
Xu, Linlin [1 ]
Jiao, Yang [2 ]
Qu, Haitao [2 ]
Ye, Jing [3 ]
机构
[1] Jinan Stomatol Hosp, Repair Dept, Jinan 250000, Shandong, Peoples R China
[2] Jinan Stomatol Hosp, Oral & Maxillofacial Surg Dept, Jinan 250000, Shandong, Peoples R China
[3] Jinan Stomatol Hosp, Orthodont Dept, Jinan 250000, Shandong, Peoples R China
关键词
compression force; human PDL; NELL1; orthodontic tooth movement; NF; K B; inflammatory response;
D O I
10.23812/j.biol.regul.homeost.agents.20243801.14
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Exogenous Nel-like molecule type 1 (NELL1) is a viable alternative in orthodontics and other fields due to its osteogenic and angiogenic properties. This study aimed to elucidate the role of NELL1 in the inflammatory response elicited by orthodontic tooth movement (OTM), providing insights into the mechanisms behind this response and establishing a theoretical foundation for the utilizing NELL1 as a therapeutic option.Methods: Human periodontal ligament (hPDL) cells obtained from clinical samples were divided into three groups: control, compressive forces (CF), and CF+ NELL1. Inflammatory factors (cyclooxygenase 2 (COX2), interleukin-6 (IL-6), interleukin8 (IL-8), tumor necrosis factor-alpha (TNF-alpha), inducible nitric oxide synthase (iNOS) and interleukin-1 beta (IL-1 beta)) were measured using real-time quantitative PCR (RT-qPCR) and enzyme-linked immunosorbent assay (ELISA). Culture supernatants were cocultured with THP-1 cells to assess macrophage differentiation. Immunoblotting and Co-Immunoprecipitation (Co-IP) assays were employed to investigate the molecular mechanism of NELL1 in hPDL cells.Results: In comparison to the CF group, the CF+ NELL1 group exhibited reduced mRNA levels and production of inflammatory factors, including COX2, IL-6, IL-8, TNF-alpha, iNOS, and IL-1 beta (p < 0.05, p < 0.01, p < 0.001, and p < 0.0001) and reduced macrophage activation (p < 0.05). Immunoblotting assays showed that NELL1 could inhibit the activation of the nuclear factorkappa B (NF-KB) signaling pathway, consequently regulating the expression of inflammatory factors (p < 0.0001, p < 0.05, p < 0.05, and p < 0.01). Co-Immunoprecipitation (Co-IP) results confirmed the intermolecular interaction between NELL1 and inhibitor of kappa B kinase (IKK), and overexpression of IKK in hPDL cells could reduce the anti-inflammatory effect of NELL1 following CF treatment (p < 0.01,p < 0.001, and p < 0.0001).Conclusions: NELL1 presents a promising therapeutic option to inhibit the activation of the NF-KB signaling pathway by preventing phosphorylation and reducing the inflammatory response during the orthodontic tooth movement.
引用
收藏
页码:187 / 199
页数:13
相关论文
共 50 条
  • [21] The transcription factor NF-KB orchestrates nucleosome remodeling during the primary response to Toll-like receptor 4 signaling
    Feng, An-Chieh
    Thomas, Brandon J.
    Purbey, Prabhat K.
    de Melo, Filipe Menegatti
    Liu, Xin
    Daly, Allison E.
    Sun, Fei
    Lo, Jerry Hung-Hao
    Cheng, Lijing
    Carey, Michael F.
    Scumpia, Philip O.
    Smale, Stephen T.
    IMMUNITY, 2024, 57 (03) : 462 - 477.e9
  • [22] MiR-1294 suppresses ROS-dependent inflammatory response in atopic dermatitis via restraining STAT3/NF-KB pathway
    Chen Yan
    Jiang Ying
    Wang Lu
    Yang Changzhi
    Qian Qihong
    Mao Jingzhu
    Sun Dongjie
    Zhu Tingting
    CELLULAR IMMUNOLOGY, 2022, 371
  • [23] LACTATE SUPPRESSES MACROPHAGE PRO-INFLAMMATORY RESPONSE TO LPS STIMULATION BY INHIBITION OF YAP AND NF-KB ACTIVATION VIA GPR81 MEDIATED SIGNALING
    Yang, Kun
    Xu, JingJing
    Tu, Fei
    Wang, Xiaohui
    Fan, Min
    Ha, Tuanzhu
    Kalbfleisch, John
    Williams, David
    Li, Chuanfu
    SHOCK, 2020, 53 : 60 - 60
  • [24] Polystyrene nanoparticles carrying miR-375 alleviate inflammatory response of intervertebral disc nucleus pulposus cells via NF-KB signaling pathway
    Zhang, Teng
    Wang, Tonghao
    Xu, Baoshan
    MATERIALS EXPRESS, 2022, 12 (06) : 794 - 801
  • [25] HYPERGLYCEMIA INDUCES INFLAMMATORY RESPONSE AND AGGRAVATES THE DEGREE OF ISCHEMIC BRAIN INJURY IN THE BODY THROUGH THE PPARF/NF-KB P65 SIGNALING PATHWAY
    Wang, Pingli
    Wang, Yongsheng
    ACTA MEDICA MEDITERRANEA, 2021, 37 (04): : 2163 - 2167
  • [26] L-selectin Promotes Migration, Invasion and Inflammatory Response of Fibroblast-Like Synoviocytes in Rheumatoid Arthritis via NF-kB Signaling Pathway
    Wu, Weijie
    Cheng, Zhen
    Nan, Yunyi
    Pan, Gang
    Wang, Youhua
    INFLAMMATION, 2025,
  • [27] Carvacrol suppresses LPS-induced pro-inflammatory activation in RAW 264.7 macrophages through ERK1/2 and NF-kB pathway
    Somensi, Nauana
    Rabelo, Thallita Kelly
    Guimaraes, Adriana Gibara
    Quintans-Junior, Lucindo Jose
    de Souza Araujo, Adriano Antunes
    Fonseca Moreira, Jose Claudio
    Gelain, Daniel Pens
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2019, 75
  • [28] Increase of transforming growth factor-beta(1) in gingival crevicular fluid during human orthodontic tooth movement
    Uematsu, S
    Mogi, M
    Deguchi, T
    ARCHIVES OF ORAL BIOLOGY, 1996, 41 (11) : 1091 - 1095
  • [29] GRg1 inhibits the TLR4/NF-kB signaling pathway by upregulating miR-216a-5p to reduce growth factors and inflammatory cytokines in DR
    Liping Xue
    Min Hu
    Qin Zhu
    Yadi Li
    Guanglong Zhou
    Xiaofan Zhang
    Yuan Zhou
    Jieying Zhang
    Peng Ding
    Molecular Biology Reports, 2023, 50 : 9379 - 9394
  • [30] GRg1 inhibits the TLR4/NF-kB signaling pathway by upregulating miR-216a-5p to reduce growth factors and inflammatory cytokines in DR
    Xue, Liping
    Hu, Min
    Zhu, Qin
    Li, Yadi
    Zhou, Guanglong
    Zhang, Xiaofan
    Zhou, Yuan
    Zhang, Jieying
    Ding, Peng
    MOLECULAR BIOLOGY REPORTS, 2023, 50 (11) : 9379 - 9394