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阿奇霉素对牙龈成纤维细胞促炎细胞因子产生及牙周组织重塑的影响。

Effect of Azithromycin on Proinflammatory Cytokine Production in Gingival Fibroblasts and the Remodeling of Periodontal Tissue.

作者信息

Nagano Takatoshi, Yamaguchi Takao, Kajiyama Sohtaro, Suzuki Takuma, Matsushima Yuji, Yashima Akihiro, Shirakawa Satoshi, Gomi Kazuhiro

机构信息

Department of Periodontology, Tsurumi University School of Dental Medicine, Yokohama 230-8501, Japan.

Aiko Yamaguchi Dental Clinic, Atsugi 243-0028, Japan.

出版信息

J Clin Med. 2020 Dec 30;10(1):99. doi: 10.3390/jcm10010099.

Abstract

Previous reports have shown that azithromycin (AZM), a macrolide antibiotic, affects collagen synthesis and cytokine production in human gingival fibroblasts (hGFs). However, there are few reports on the effect of AZM on human periodontal ligament fibroblasts (hPLFs). In the present study, we comparatively examined the effects of AZM on hGFs and hPLFs. We monitored the reaction of AZM under lipopolysaccharide (LPS) stimulation or no stimulation in hGFs and hPLFs. Gene expression analyses of interleukin-6 (IL-6), interleukin-8 (IL-8), matrix metalloproteinase-1 (MMP-1), matrix metalloproteinase-2 (MMP-2), and Type 1 collagen were performed using reverse transcription-polymerase chain reaction (RT-PCR). Subsequently, we performed Western blotting for the analysis of the intracellular signal transduction pathway. In response to LPS stimulation, the gene expression levels of IL-6 and IL-8 in hGFs increased due to AZM in a concentration-dependent manner, and phosphorylation of nuclear factor kappa B (NF-κB) was also promoted. Additionally, AZM caused an increase in MMP-1 expression in hGFs, whereas it did not affect the expression of any of the analyzed genes in hPLFs. Our findings indicate that AZM does not affect hPLFs and acts specifically on hGFs. Thus, AZM may increase the expression of IL-6 and IL-8 under LPS stimulation to modify the inflammatory response and increase the expression of MMP-1 to promote connective tissue remodeling.

摘要

先前的报告显示,大环内酯类抗生素阿奇霉素(AZM)会影响人牙龈成纤维细胞(hGFs)中的胶原蛋白合成和细胞因子产生。然而,关于AZM对人牙周膜成纤维细胞(hPLFs)影响的报道较少。在本研究中,我们比较研究了AZM对hGFs和hPLFs的影响。我们监测了在脂多糖(LPS)刺激或无刺激情况下AZM在hGFs和hPLFs中的反应。使用逆转录-聚合酶链反应(RT-PCR)对白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、基质金属蛋白酶-1(MMP-1)、基质金属蛋白酶-2(MMP-2)和I型胶原蛋白进行基因表达分析。随后,我们进行蛋白质免疫印迹以分析细胞内信号转导途径。响应LPS刺激,hGFs中IL-6和IL-8的基因表达水平因AZM呈浓度依赖性增加,并且核因子κB(NF-κB)的磷酸化也得到促进。此外,AZM导致hGFs中MMP-1表达增加,而它不影响hPLFs中任何分析基因的表达。我们的研究结果表明,AZM不影响hPLFs,而是特异性作用于hGFs。因此,AZM可能在LPS刺激下增加IL-6和IL-8的表达以改变炎症反应,并增加MMP-1的表达以促进结缔组织重塑。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8812/7794813/f42c30c399fb/jcm-10-00099-g001.jpg

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