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多聚胺诱导蛋白酪氨酸磷酸酶非受体型 2 激活发挥抗炎症作用,在人单核细胞 THP-1 和小鼠急性结肠炎模型中。

Activation of protein tyrosine phosphatase non-receptor type 2 by spermidine exerts anti-inflammatory effects in human THP-1 monocytes and in a mouse model of acute colitis.

机构信息

Division of Gastroenterology and Hepatology, University Hospital Zurich, Zurich, Switzerland.

出版信息

PLoS One. 2013 Sep 9;8(9):e73703. doi: 10.1371/journal.pone.0073703. eCollection 2013.

Abstract

BACKGROUND

Spermidine is a dietary polyamine that is able to activate protein tyrosine phosphatase non-receptor type 2 (PTPN2). As PTPN2 is known to be a negative regulator of interferon-gamma (IFN-γ)-induced responses, and IFN-γ stimulation of immune cells is a critical process in the immunopathology of inflammatory bowel disease (IBD), we wished to explore the potential of spermidine for reducing pro-inflammatory effects in vitro and in vivo.

METHODS

Human THP-1 monocytes were treated with IFN-γ and/or spermidine. Protein expression and phosphorylation were analyzed by Western blot, cytokine expression by quantitative-PCR, and cytokine secretion by ELISA. Colitis was induced in mice by dextran sodium sulfate (DSS) administration. Disease severity was assessed by recording body weight, colonoscopy and histology.

RESULTS

Spermidine increased expression and activity of PTPN2 in THP-1 monocytes and reduced IFN-γ-induced phosphorylation of signal transducer and activator of transcription (STAT) 1 and 3, as well as p38 mitogen-activated protein kinase (MAPK) in a PTPN2 dependent manner. Subsequently, IFN-γ-induced expression/secretion of intracellular cell adhesion molecule (ICAM)-1 mRNA, monocyte chemoattractant protein (MCP)-1, and interleukin (IL)-6 was reduced in spermidine-treated cells. The latter effects were absent in PTPN2-knockdown cells. In mice with DSS-induced colitis, spermidine treatment resulted in ameliorated weight loss and decreased mucosal damage indicating reduced disease severity.

CONCLUSIONS

Activation of PTPN2 by spermidine ameliorates IFN-γ-induced inflammatory responses in THP-1 cells. Furthermore, spermidine treatment significantly reduces disease severity in mice with DSS-induced colitis; hence, spermidine supplementation and subsequent PTPN2 activation may be helpful in the treatment of chronic intestinal inflammation such as IBD.

摘要

背景

亚精胺是一种膳食多胺,能够激活蛋白酪氨酸磷酸酶非受体型 2(PTPN2)。由于 PTPN2 是干扰素-γ(IFN-γ)诱导反应的负调节剂,而 IFN-γ 刺激免疫细胞是炎症性肠病(IBD)免疫病理学的关键过程,我们希望探索亚精胺在体外和体内减少促炎作用的潜力。

方法

用 IFN-γ 和/或亚精胺处理人 THP-1 单核细胞。通过 Western blot 分析蛋白表达和磷酸化,通过定量-PCR 分析细胞因子表达,通过 ELISA 分析细胞因子分泌。用葡聚糖硫酸钠(DSS)给药诱导小鼠结肠炎。通过记录体重、结肠镜检查和组织学评估疾病严重程度。

结果

亚精胺增加了 THP-1 单核细胞中 PTPN2 的表达和活性,并以 PTPN2 依赖的方式减少了 IFN-γ 诱导的信号转导和转录激活因子(STAT)1 和 3以及丝裂原活化蛋白激酶(MAPK)p38 的磷酸化。随后,IFN-γ 诱导的细胞内细胞间黏附分子(ICAM)-1 mRNA、单核细胞趋化蛋白(MCP)-1 和白细胞介素(IL)-6 的表达/分泌在亚精胺处理的细胞中减少。在 PTPN2 敲低细胞中不存在这些作用。在 DSS 诱导的结肠炎小鼠中,亚精胺治疗导致体重减轻减轻和粘膜损伤减少,表明疾病严重程度降低。

结论

亚精胺通过激活 PTPN2 改善了 THP-1 细胞中 IFN-γ 诱导的炎症反应。此外,亚精胺治疗显著降低了 DSS 诱导的结肠炎小鼠的疾病严重程度;因此,亚精胺补充和随后的 PTPN2 激活可能有助于治疗慢性肠道炎症,如 IBD。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1430/3767590/919d157205b5/pone.0073703.g001.jpg

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