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口腔微生物与宿主的相互作用:β-葡聚糖对炎性细胞因子基因表达和代谢组谱的影响

Oral microbe-host interactions: influence of β-glucans on gene expression of inflammatory cytokines and metabolome profile.

作者信息

Silva Viviam de Oliveira, Pereira Luciano José, Murata Ramiro Mendonça

机构信息

Herman Ostrow School of Dentistry, Division of Periodontology Diagnostic Sciences, Dental Hygiene & Biomedical Science, University of Southern California, Los Angeles, CA, USA.

Department of Veterinary Medicine, Physiology and Pharmacology Area, Federal University of Lavras, Lavras, Minas Gerais, Brazil.

出版信息

BMC Microbiol. 2017 Mar 7;17(1):53. doi: 10.1186/s12866-017-0946-1.

DOI:10.1186/s12866-017-0946-1
PMID:28270109
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5341410/
Abstract

BACKGROUND

The aim of this study was to evaluate the effects of β-glucan on the expression of inflammatory mediators and metabolomic profile of oral cells [keratinocytes (OBA-9) and fibroblasts (HGF-1) in a dual-chamber model] infected by Aggregatibacter actinomycetemcomitans. The periodontopathogen was applied and allowed to cross the top layer of cells (OBA-9) to reach the bottom layer of cells (HGF-1) and induce the synthesis of immune factors and cytokines in the host cells. β-glucan (10 μg/mL or 20 μg/mL) were added, and the transcriptional factors and metabolites produced were quantified in the remaining cell layers and supernatant.

RESULTS

The relative expression of interleukin (IL)-1-α and IL-18 genes in HGF-1 decreased with 10 μg/mL or 20 μg/mL of β-glucan, where as the expression of PTGS-2 decreased only with 10 μg/mL. The expression of IL-1-α increased with 20 μg/mL and that of IL-18 increased with 10 μg/mL in OBA-9; the expression of BCL 2, EP 300, and PTGS-2 decreased with the higher dose of β-glucan. The production of the metabolite 4-aminobutyric acid presented lower concentrations under 20 μg/mL, whereas the concentrations of 2-deoxytetronic acid NIST and oxalic acid decreased at both concentrations used. Acetophenone, benzoic acid, and pinitol presented reduced concentrations only when treated with 10 μg/mL of β-glucan.

CONCLUSIONS

Treatment with β-glucans positively modulated the immune response and production of metabolites.

摘要

背景

本研究旨在评估β-葡聚糖对受伴放线聚集杆菌感染的口腔细胞(双室模型中的角质形成细胞(OBA-9)和成纤维细胞(HGF-1))中炎症介质表达和代谢组学特征的影响。应用牙周病原体并使其穿过细胞顶层(OBA-9)到达细胞底层(HGF-1),诱导宿主细胞中免疫因子和细胞因子的合成。添加β-葡聚糖(10μg/mL或20μg/mL),并对剩余细胞层和上清液中产生的转录因子和代谢产物进行定量。

结果

在HGF-1中,10μg/mL或20μg/mL的β-葡聚糖可使白细胞介素(IL)-1-α和IL-18基因的相对表达降低,而PTGS-2的表达仅在10μg/mL时降低。在OBA-9中,20μg/mL时IL-1-α的表达增加,10μg/mL时IL-18的表达增加;较高剂量的β-葡聚糖可使BCL 2、EP 300和PTGS-2的表达降低。代谢产物4-氨基丁酸的产生在20μg/mL以下时浓度较低,而在两种使用浓度下,2-脱氧四糖酸NIST和草酸的浓度均降低。仅在使用10μg/mL的β-葡聚糖处理时,苯乙酮、苯甲酸和松醇的浓度降低。

结论

β-葡聚糖处理可正向调节免疫反应和代谢产物的产生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/9cfe21202dc3/12866_2017_946_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/61a1ff53e25d/12866_2017_946_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/f153fdcfe66b/12866_2017_946_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/d50175b0945b/12866_2017_946_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/eceb7f8f11b9/12866_2017_946_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/9cfe21202dc3/12866_2017_946_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/61a1ff53e25d/12866_2017_946_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/f153fdcfe66b/12866_2017_946_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/d50175b0945b/12866_2017_946_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/eceb7f8f11b9/12866_2017_946_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3717/5341410/9cfe21202dc3/12866_2017_946_Fig5_HTML.jpg

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