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谷胱甘肽三硫化物可预防脂多糖诱导的视网膜色素上皮细胞炎症基因表达。

Glutathione Trisulfide Prevents Lipopolysaccharide-induced Inflammatory Gene Expression in Retinal Pigment Epithelial Cells.

机构信息

Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.

Department of Retinal Disease Control, Tohoku University Graduate School of Medicine, Sendai, Japan.

出版信息

Ocul Immunol Inflamm. 2022 May 19;30(4):789-800. doi: 10.1080/09273948.2020.1833224. Epub 2020 Nov 20.

Abstract

We investigated the effects of glutathione trisulfide (GSSSG) on lipopolysaccharide (LPS)-induced inflammatory gene expression in immortalized ARPE-19, and primary human and mouse retinal pigment epithelial (RPE) cells. Sulfane sulfur molecules were significantly increased in GSSSG-treated ARPE-19 cells. GSSSG prevented the LPS-induced upregulation of ()-, and () in ARPE-19/primary RPE cells. Moreover, GSSSG prevented the activation of the nuclear factor-kappa B p65 subunit, and promoted the activation of extracellular signal-regulated kinase 1/2 (ERK1/2) in LPS-treated ARPE-19 cells. ERK1/2 inhibition prevented the GSSSG-mediated inhibition of LPS-induced and upregulation. Additionally, ERK1/2 activation prevented the upregulation of these genes in the absence of GSSSG. Knockdown of or , known as anti-oxidative genes, did not affect the activity of GSSSG in the context of LPS stimulation. These findings suggest that GSSSG attenuates LPS-induced inflammatory gene expression via ERK signaling hyperactivation, independently of the NRF2/HMOX1 pathway.

摘要

我们研究了谷胱甘肽三硫化物(GSSSG)对脂多糖(LPS)诱导的永生化 ARPE-19 细胞、原代人源和鼠源视网膜色素上皮(RPE)细胞中炎症基因表达的影响。GSSSG 处理的 ARPE-19 细胞中硫磺酸分子显著增加。GSSSG 可预防 LPS 诱导的 ARPE-19/原代 RPE 细胞中 ()-和 () 的上调。此外,GSSSG 可预防 LPS 处理的 ARPE-19 细胞中核因子-κB p65 亚基的激活,并促进细胞外信号调节激酶 1/2(ERK1/2)的激活。ERK1/2 的抑制可阻止 GSSSG 介导的 LPS 诱导的 和 上调。此外,ERK1/2 的激活可阻止在没有 GSSSG 的情况下这些基因的上调。已知抗氧化基因 或 的敲低在 LPS 刺激的情况下并不影响 GSSSG 的活性。这些发现表明,GSSSG 通过 ERK 信号的过度激活来减轻 LPS 诱导的炎症基因表达,而不依赖于 NRF2/HMOX1 通路。

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