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来自被感染的人类巨噬细胞的色氨酰tRNA合成酶诱导与动脉粥样硬化相关的促炎反应。

Tryptophanyl tRNA Synthetase from Human Macrophages Infected by Induces a Proinflammatory Response Associated with Atherosclerosis.

作者信息

Sasaki Minoru, Shimoyama Yu, Kodama Yoshitoyo, Ishikawa Taichi

机构信息

Department of Microbiology, Division of Molecular Microbiology, Iwate Medical University, Morioka 028-3694, Japan.

出版信息

Pathogens. 2021 Dec 20;10(12):1648. doi: 10.3390/pathogens10121648.

DOI:10.3390/pathogens10121648
PMID:34959604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8708850/
Abstract

is the most common microorganism associated with adult periodontal disease, causing inflammation around the subgingival lesion. In this study, we investigated tryptophanyl tRNA synthase (WRS) production by THP-1 cells infected with . Cytokine production, leukocyte adhesion molecules, and low-density lipoprotein receptor (LDLR) expressions in cultured cells were examined. WRS was detected in THP-1 cell culture supernatants stimulated with from 1 to 24 h, and apparent production was observed after 4 h. No change in WRS mRNA expression was observed from 1 to 6 h in THP-1 cells, whereas its expression was significantly increased 12 h after stimulation with . Lactate dehydrogenase (LDH) activity was observed from 4 to 24 h. The TNF-α, IL-6, IL-8, and CXCL2 levels of THP-1 cells were upregulated after treatment with recombinant WRS (rWRS) and were significantly reduced when THP-1 cells were treated with C29. The MCP-1, ICAM-1, and VCAM-1 levels in human umbilical vein endothelial cells were upregulated following treatment with rWRS, and TAK242 suppressed these effects. Additionally, unmodified LDLR, macrophage scavenger receptor A, and lectin-like oxidized LDLRs were upregulated in THP-1 cells treated with rWRS. These results suggest that WRS from macrophages infected with is associated with atherosclerosis.

摘要

是与成人牙周病相关的最常见微生物,可导致龈下病变周围的炎症。在本研究中,我们调查了感染 的THP-1细胞产生色氨酰tRNA合成酶(WRS)的情况。检测了培养细胞中的细胞因子产生、白细胞粘附分子和低密度脂蛋白受体(LDLR)表达。在用 刺激THP-1细胞培养上清液1至24小时后检测到WRS,4小时后观察到明显产生。在THP-1细胞中,从1至6小时未观察到WRS mRNA表达的变化,而在用 刺激12小时后其表达显著增加。在4至24小时观察到乳酸脱氢酶(LDH)活性。用重组WRS(rWRS)处理后,THP-1细胞的TNF-α、IL-6、IL-8和CXCL2水平上调,而用C29处理THP-1细胞时这些水平显著降低。用rWRS处理后人脐静脉内皮细胞中的MCP-1、ICAM-1和VCAM-1水平上调,TAK242抑制了这些作用。此外,在用rWRS处理的THP-1细胞中,未修饰的LDLR、巨噬细胞清道夫受体A和凝集素样氧化LDLR上调。这些结果表明,感染 的巨噬细胞产生的WRS与动脉粥样硬化有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/57e9839d22de/pathogens-10-01648-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/c2e3bded447b/pathogens-10-01648-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/ea68a4fb4e80/pathogens-10-01648-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/17657d2ba914/pathogens-10-01648-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/634a6e77b22d/pathogens-10-01648-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/d4500d5827ef/pathogens-10-01648-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/57e9839d22de/pathogens-10-01648-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/c2e3bded447b/pathogens-10-01648-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/ea68a4fb4e80/pathogens-10-01648-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/17657d2ba914/pathogens-10-01648-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/634a6e77b22d/pathogens-10-01648-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/d4500d5827ef/pathogens-10-01648-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8ff/8708850/57e9839d22de/pathogens-10-01648-g006.jpg

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