KAT6A促进巨噬细胞炎症和牙周炎

IF 5.8 1区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Shi‐Jia Huang, Shuo Xu, Hui‐Lin Ye, Lu‐Jun Zhou, Yong‐Li Wang, Sheng‐Zhong Duan
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引用次数: 0

摘要

表观遗传修饰和免疫调节在牙周炎(PD)中起重要作用。然而,巨噬细胞赖氨酸乙酰转移酶6A (KAT6A)在PD中的功能尚不清楚。在这项研究中,我们首先分析了单细胞RNA测序数据,并证明了PD患者牙周组织巨噬细胞中KAT6A表达上调。随后,产生巨噬细胞KAT6A敲除(MK6AKO)小鼠,并通过磨牙结扎和应用牙龈卟啉单胞菌(Pg)联合诱导PD。形态学分析显示,MK6AKO小鼠的牙槽骨吸收明显减少,qRT - PCR分析显示,与同窝小鼠相比,PD诱导后MK6AKO小鼠的牙龈炎症基因表达明显减弱。用Pg脂多糖(Pg‐LPS)刺激的腹膜巨噬细胞的RNA‐seq揭示了炎症通路的下调,特别是MK6AKO巨噬细胞的白细胞介素17通路。流式细胞术分析发现,PD诱导后MK6AKO小鼠牙龈中性粒细胞明显减少。此外,使用Cut&;tag技术,我们发现Pg‐LPS处理的MK6AKO巨噬细胞中,白细胞介素1β和肿瘤坏死因子启动子上核因子kappa‐B结合位点的组蛋白H3K27乙酰化水平降低。综上所述,我们的研究强调了KAT6A在调节巨噬细胞表型和PD进展中的重要作用,提示靶向KAT6A的治疗潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
KAT6A Promotes Macrophage Inflammation and Periodontitis
Both epigenetic modification and immunoregulation play important roles in periodontitis (PD). However, the function of macrophage lysine acetyltransferase 6A (KAT6A) in PD remains unknown. In this study, we first analysed single‐cell RNA sequencing data and demonstrated up‐regulated KAT6A expression in periodontal tissue macrophages of PD patients. Subsequently, macrophage KAT6A knockout (MK6AKO) mice were generated and subjected to PD induction by a combination of molar ligation and application of Porphyromonas gingivalis (Pg). Morphological analyses showed significantly decreased alveolar bone resorption in MK6AKO mice, and qRT‐PCR analysis showed markedly attenuated expression of inflammatory genes in the gingiva of MK6AKO mice compared to littermate mice after PD induction. RNA‐seq of peritoneal macrophages stimulated with Pg lipopolysaccharides (Pg‐LPS) unveiled down‐regulation of inflammatory pathways, particularly the interleukin 17 pathway in MK6AKO macrophages. Flow cytometry analysis detected a notable reduction of neutrophils in the gingiva of MK6AKO mice after PD induction. Furthermore, using the Cut&tag technique, we identified reduced histone H3K27 acetylation levels at nuclear factor kappa‐B binding sites on promoters of interleukin 1β and tumour necrosis factor in MK6AKO macrophages treated with Pg‐LPS. In summary, our study highlights the significant role of KAT6A in modulating macrophage phenotypes and the progression of PD, suggesting the therapeutic potential of targeting KAT6A.
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来源期刊
Journal of Clinical Periodontology
Journal of Clinical Periodontology 医学-牙科与口腔外科
CiteScore
13.30
自引率
10.40%
发文量
175
审稿时长
3-8 weeks
期刊介绍: Journal of Clinical Periodontology was founded by the British, Dutch, French, German, Scandinavian, and Swiss Societies of Periodontology. The aim of the Journal of Clinical Periodontology is to provide the platform for exchange of scientific and clinical progress in the field of Periodontology and allied disciplines, and to do so at the highest possible level. The Journal also aims to facilitate the application of new scientific knowledge to the daily practice of the concerned disciplines and addresses both practicing clinicians and academics. The Journal is the official publication of the European Federation of Periodontology but wishes to retain its international scope. The Journal publishes original contributions of high scientific merit in the fields of periodontology and implant dentistry. Its scope encompasses the physiology and pathology of the periodontium, the tissue integration of dental implants, the biology and the modulation of periodontal and alveolar bone healing and regeneration, diagnosis, epidemiology, prevention and therapy of periodontal disease, the clinical aspects of tooth replacement with dental implants, and the comprehensive rehabilitation of the periodontal patient. Review articles by experts on new developments in basic and applied periodontal science and associated dental disciplines, advances in periodontal or implant techniques and procedures, and case reports which illustrate important new information are also welcome.
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