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抑制素配体IN44可减轻牙龈卟啉单胞菌介导的炎症。

The prohibitin ligand IN44 decreases Porphyromonas gingivalis mediated inflammation.

作者信息

Stutz Céline, Gegout Pierre-Yves, Bloch Chloé, Özçelik Hayriye, Anton Nicolas, Tabti Redouane, Désaubry Laurent, Huck Olivier, Petit Catherine

机构信息

INSERM (French National Institute of Health and Medical Research), UMR 1260, Regenerative Nanomedicine, CRBS, 1 Rue Eugène Boeckel, Strasbourg, 67084, France.

Faculté de Chirurgie-dentaire, Dental Faculty, Université de Strasbourg, 8 rue Sainte-Elisabeth, Strasbourg, 67000, France.

出版信息

BMC Oral Health. 2024 Dec 21;24(1):1534. doi: 10.1186/s12903-024-05209-2.

Abstract

BACKGROUND

Periodontitis is an inflammatory disease causing destruction of periodontal tissues. Controlling inflammation is crucial for periodontitis treatment. Prohibitins (PHBs) are emerging targets in the treatment of inflammatory diseases. To identify compounds that would alleviate periodontitis, several small molecules that directly target PHBs and display various pharmacological activities were screened to decrease Porphyromonas gingivalis induced inflammation. Indeed, IN44, a new PHB ligand that has been shown to inhibit STAT3 and NF-kB signaling, suggesting that it may alleviate periodontitis. This study aimed to assess IN44's impact on inflammation elicited by P. gingivalis.

METHODS

In vitro, IN44 cytotoxicity was tested on periodontal cells with AlamarBlue and Live/Dead assays. Its effect on cytokines and mitochondrial ROS production were evaluated using ELISA and Mitosox assay. In mouse, systemic inflammation and experimental periodontitis were induced to assess IN44's therapeutic effects.

RESULTS

In vitro, IN44 (50 µM) showed no cytotoxicity on periodontal cells. It significantly reduced pro-inflammatory cytokine secretion and mitochondrial ROS in P. gingivalis-infected epithelial cells. Proteome analysis on infected epithelial cells revealed modulation of HSP60 and Akt expression by IN44. In vivo, IN44 demonstrated anti-inflammatory effects in a mouse model of systemic inflammation induced by P. gingivalis, and it improved periodontal healing.

CONCLUSION

These findings suggest that PHBs may warrant consideration as therapeutic targets for periodontitis and possibly other inflammatory disorders.

摘要

背景

牙周炎是一种导致牙周组织破坏的炎症性疾病。控制炎症对于牙周炎治疗至关重要。 prohibitin(PHB)是炎症性疾病治疗中新兴的靶点。为了鉴定可缓解牙周炎的化合物,筛选了几种直接靶向PHB并具有多种药理活性的小分子,以减少牙龈卟啉单胞菌诱导的炎症。实际上,IN44是一种新的PHB配体,已被证明可抑制STAT3和NF-κB信号传导,这表明它可能缓解牙周炎。本研究旨在评估IN44对牙龈卟啉单胞菌引发的炎症的影响。

方法

在体外,使用AlamarBlue和活/死检测法检测IN44对牙周细胞的细胞毒性。使用ELISA和Mitosox检测法评估其对细胞因子和线粒体ROS产生的影响。在小鼠中,诱导全身性炎症和实验性牙周炎以评估IN44的治疗效果。

结果

在体外,IN44(50μM)对牙周细胞无细胞毒性。它显著降低了牙龈卟啉单胞菌感染的上皮细胞中促炎细胞因子的分泌和线粒体ROS。对感染上皮细胞的蛋白质组分析显示IN44对HSP60和Akt表达有调节作用。在体内,IN44在牙龈卟啉单胞菌诱导的全身性炎症小鼠模型中表现出抗炎作用,并改善了牙周愈合。

结论

这些发现表明,PHB可能值得作为牙周炎以及可能其他炎症性疾病的治疗靶点加以考虑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe64/11662793/9673f9b66a9a/12903_2024_5209_Fig1_HTML.jpg

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