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成纤维细胞生长因子-2 抑制 CD40 介导的牙周炎症。

Fibroblast growth factor-2 inhibits CD40-mediated periodontal inflammation.

机构信息

Department of Periodontology, Osaka University Graduate School of Dentistry, Osaka, Japan.

Division of Periodontology and Endodontology, Tohoku University Graduate School of Dentistry, Miyagi, Japan.

出版信息

J Cell Physiol. 2019 May;234(5):7149-7160. doi: 10.1002/jcp.27469. Epub 2018 Oct 28.

Abstract

Fibroblast growth factor-2 (FGF-2) stimulates periodontal regeneration by a broad spectrum of effects on periodontal ligament (PDL) cells, such as proliferation, migration, and production of extracellular matrix. A critical factor in the success of periodontal regeneration is the rapid resolution of inflammatory responses in the tissue. We explored an anti-inflammatory effect of FGF-2 during periodontal regeneration and healing. We found that FGF-2 on mouse periodontal ligament cells (MPDL22) markedly downregulated CD40 expression, a key player of inflammation. In addition, FGF-2 inhibited CD40 signaling by the non-canonical nuclear factor-kappa B2 (NFκB2) pathway, resulting in decreased production of interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α), which have the potential to recruit immune cells to inflamed sites. Furthermore, in vivo treatment of FGF-2 enhanced healing of skin wounds by counteracting the CD40-mediated inflammation. These results reveal that FGF-2 has an important function as a negative regulator of inflammation during periodontal regeneration and healing.

摘要

成纤维细胞生长因子-2(FGF-2)通过对牙周韧带(PDL)细胞的多种作用刺激牙周再生,如增殖、迁移和细胞外基质的产生。牙周再生和愈合成功的一个关键因素是组织中炎症反应的迅速解决。我们探讨了 FGF-2 在牙周再生和愈合过程中的抗炎作用。我们发现 FGF-2 可显著下调牙周韧带细胞(MPDL22)上 CD40 的表达,CD40 是炎症的关键参与者。此外,FGF-2 通过非经典核因子-κB2(NFκB2)途径抑制 CD40 信号转导,导致白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)的产生减少,这些因子有可能招募免疫细胞到炎症部位。此外,体内给予 FGF-2 治疗可通过拮抗 CD40 介导的炎症来增强皮肤伤口的愈合。这些结果表明,FGF-2 在牙周再生和愈合过程中作为炎症的负调节剂具有重要功能。

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