Department of Ophthalmology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Retinal Disease Control, Tohoku University Graduate School of Medicine, Sendai, Japan.
Ocul Immunol Inflamm. 2022 May 19;30(4):789-800. doi: 10.1080/09273948.2020.1833224. Epub 2020 Nov 20.
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.
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。