Department of Gastroenterology and Metabology, Ehime University Graduate School of Medicine, Shitsukawa, Toon, Ehime, Japan.
PLoS One. 2019 Feb 22;14(2):e0212589. doi: 10.1371/journal.pone.0212589. eCollection 2019.
Hepatic stellate cells (HSCs) were reported to promote the progression of hepatocellular carcinoma (HCC), however its mechanism is uncertain. We previously reported that protein kinase R (PKR) in hepatocytes regulated HCC proliferation. In this study, we focused on the role of PKR in HSCs, and clarified the mechanism of its association with HCC progression. We confirmed the activation of PKR in a human HSC cell line (LX-2 cell). IL-1β is produced from HSCs stimulated by lipopolysaccharide (LPS) or palmitic acid which are likely activators of PKR in non-alcoholic steatohepatitis (NASH). Production was assessed by real-time PCR and ELISA. C16 and small interfering RNA (siRNA) were used to inhibit PKR in HSCs. The HCC cell line (HepG2 cell) was cultured with HSC conditioning medium to assess HCC progression, which was evaluated by proliferation and scratch assays. Expression of PKR was increased and activated in stimulated HSCs, and IL-1β production was also increased molecular. Key molecules of the mitogen-activated protein kinase pathway were also upregulated and activated by LPS. Otherwise, PKR inhibition by C16 and PKR siRNA decreased IL-1β production. HCC progression was promoted by HSC-stimulated conditioning medium although it was reduced by the conditioning medium from PKR-inhibited HSCs. Moreover, palmitic acid also upregulated IL-1β expression in HSCs, and conditioning medium from palmitic acid-stimulated HSCs promoted HCC proliferation. Stimulated HSCs by activators of PKR in NASH could play a role in promoting HCC progression through the production of IL-1β, via a mechanism that seems to be dependent on PKR activation.
肝星状细胞(HSCs)被报道促进肝细胞癌(HCC)的进展,但其机制尚不确定。我们之前报道过肝细胞中的蛋白激酶 R(PKR)调节 HCC 的增殖。在这项研究中,我们专注于 PKR 在 HSCs 中的作用,并阐明了其与 HCC 进展相关的机制。我们证实了人 HSC 细胞系(LX-2 细胞)中 PKR 的激活。白细胞介素-1β(IL-1β)由脂多糖(LPS)或棕榈酸刺激的 HSCs 产生,这些物质可能是非酒精性脂肪性肝炎(NASH)中 PKR 的激活剂。通过实时 PCR 和 ELISA 评估其产生情况。使用 C16 和小干扰 RNA(siRNA)抑制 HSCs 中的 PKR。将 HCC 细胞系(HepG2 细胞)与 HSC 条件培养基共培养,以评估 HCC 进展,通过增殖和划痕实验进行评估。刺激的 HSCs 中 PKR 的表达增加并被激活,IL-1β 的产生也增加。LPS 还上调并激活丝裂原活化蛋白激酶途径的关键分子。相反,C16 和 PKR siRNA 抑制 PKR 减少了 IL-1β 的产生。尽管受 PKR 抑制的 HSCs 的条件培养基减少了 HCC 进展,但 HSC 刺激的条件培养基促进了 HCC 的增殖。NASH 中 PKR 的激活剂刺激的 HSCs 通过产生 IL-1β 可能在促进 HCC 进展中发挥作用,其机制似乎依赖于 PKR 的激活。