Department of Anesthesia, Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, 150, Ximen Street, Linhai City, Taizhou, 317000, Zhejiang, China.
Department of Anesthesia, The First Affiliated Hospital of Zhejiang Chinese Medical University (Zhejiang Provincial Hospital of Chinese Medicine), Hangzhou, 310000, Zhejiang, China.
Sci Rep. 2023 Jul 24;13(1):11913. doi: 10.1038/s41598-023-38852-w.
Acute liver injury (ALI) may manifest at any phase of sepsis, yet an explicit therapeutic approach remains elusive. In this study, LPS and cecum ligation and puncture (CLP) were utilized to establish an inflammatory cell model and a murine model of sepsis-induced liver injury, respectively, aiming to explore the potential protective effect of protein interacting with C α kinase 1 (PICK1) on sepsis-induced ALI and its underlying mechanisms. In both the cell supernatant and the murine whole blood, the concentrations of inflammatory factors were quantified by ELISA, while the protein and mRNA expressions of PICK1, cleaved-PARP-1, caspase1, TLR4, IκBα, and NF-κB were assessed via western blot and qRT-PCR. The outcomes revealed that the knockdown of PICK1 increased the levels of inflammatory factors and apoptosis, alongside activation of TLR4/NF-κB signaling pathway-related factors in both in vivo and in vitro models. Moreover, the murine liver samples were subjected to Hematoxylin-Eosin (HE) staining for assessment of histopathological morphology. The HE staining and liver injury scoring results manifested a markedly exacerbated hepatic damage in PICK1 knockout mice as compared to WT mice following CLP. Furthermore, the liver macrophages were isolated from murine livers, and the expression and activity of the factors associated with the TLR4/NF-κB signaling pathway were verified through RT-qPCR and western blot, and EMSA assay demonstrated an augmented NF-κB activity subsequent to PICK1 knockout. Finally, the expression and localization of PICK1 in macrophages were further scrutinized via immunofluorescence, and the interaction between PICK1 and TLR4 was identified through co-immunoprecipitation. In conclusion, the knockdown of PICK1 appeared to modulate inflammatory factors by activating the TLR4/NF-κB signaling pathway, thereby exacerbating hepatic damage induced by sepsis.
急性肝损伤(ALI)可能在脓毒症的任何阶段表现出来,但明确的治疗方法仍难以捉摸。在这项研究中,分别使用 LPS 和盲肠结扎穿孔(CLP)建立了炎症细胞模型和脓毒症诱导的肝损伤小鼠模型,旨在探讨蛋白相互作用的 Cα激酶 1(PICK1)对脓毒症诱导的 ALI 的潜在保护作用及其潜在机制。通过 ELISA 定量测定细胞上清液和小鼠全血中炎症因子的浓度,通过 Western blot 和 qRT-PCR 测定 PICK1、裂解型 PARP-1、caspase1、TLR4、IκBα 和 NF-κB 的蛋白和 mRNA 表达。结果表明,在体内和体外模型中,敲低 PICK1 会增加炎症因子和细胞凋亡水平,并激活 TLR4/NF-κB 信号通路相关因子。此外,对小鼠肝组织进行苏木精-伊红(HE)染色,评估组织病理学形态。HE 染色和肝损伤评分结果表明,与 WT 小鼠相比,CLP 后 PICK1 基因敲除小鼠的肝损伤明显加重。此外,从小鼠肝脏中分离出肝巨噬细胞,通过 RT-qPCR 和 Western blot 验证与 TLR4/NF-κB 信号通路相关的因子的表达和活性,EMSA 实验表明 PICK1 基因敲除后 NF-κB 活性增强。最后,通过免疫荧光进一步研究巨噬细胞中 PICK1 的表达和定位,并通过共免疫沉淀鉴定 PICK1 和 TLR4 之间的相互作用。综上所述,敲低 PICK1 通过激活 TLR4/NF-κB 信号通路来调节炎症因子,从而加重脓毒症引起的肝损伤。