Department of Surgery, School of Medicine, Kurume University, Fukuoka, Japan.
Anticancer Res. 2013 Jul;33(7):2887-94.
Heat-shock proteins (HSPs) are members of a chaperone protein family reported to modify stress responses. The aim of this study was to clarify the hypothesis of whether pre-treatment with heat shock reduces liver damage and influences liver regeneration after partial hepatectomy.
Mice (N=6) were divided into two groups: the control group underwent partial hepatectomy without heat shock pre-treatment, the heat shock (HS) group underwent partial hepatectomy 12 hours after pre-treatment with heat shock. Mice were sacrificed at different time points after hepatectomy, remnant liver and blood were collected for further analyses in blood samples and liver tissues. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), interleukin-6 (IL6), and tumor necrosis factor-alpha (TNFα) were measured using enzyme-linked immunosorbent assay (ELISA). We used tissue samples for several experiments: staining by 5-bromo-2-deoxyuridine (BrdU), evaluation of cytokines, transcription factors and signal-transduction associated proteins.
HSP70 levels in the liver were clearly increased from 6 h to 72 h after heat shock treatment. Serum ALT and AST levels were significantly reduced in the HS group compared to the control group after partial hepatectomy. Liver regeneration rate and BrdU labeling index were significantly higher in the HS group than in the control group after partial hepatectomy. IL6 and TNFα in serum and liver tissues were significantly reduced in the HS group compared to the control group after hepatectomy. We did not detect phosphorylation of signal transducer and activator of transcription-3 (STAT3) protein by western blotting. Binding activities of transcription factors: nuclear factor-interleukin-6 (NF-IL6) and nuclear factor-kappa B (NF-kB) were significantly lower in the HS group than in the control group after hepatectomy.
Pre-treatment with heat shock appears to reduce liver injury and promote liver regeneration, as HSP70 can reduce the inflammatory response and up-regulate liver regeneration without IL6 STAT signaling pathway in the liver after partial hepatectomy.
热休克蛋白(HSPs)是伴侣蛋白家族的成员,据报道其可以调节应激反应。本研究旨在阐明热休克预处理是否可以减轻肝损伤并影响部分肝切除后的肝再生。
将小鼠(N=6)分为两组:对照组未进行热休克预处理行部分肝切除术,热休克(HS)组在预处理后 12 小时行部分肝切除术。在肝切除术后的不同时间点处死小鼠,收集残余肝和血液,用于进一步分析血液样本和肝组织。采用酶联免疫吸附试验(ELISA)检测天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)、白细胞介素-6(IL6)和肿瘤坏死因子-α(TNFα)。我们使用组织样本进行了几项实验:5-溴-2-脱氧尿苷(BrdU)染色、细胞因子、转录因子和信号转导相关蛋白的评估。
热休克处理后,肝组织中 HSP70 水平从 6 小时到 72 小时明显升高。与对照组相比,部分肝切除术后 HS 组血清 ALT 和 AST 水平显著降低。与对照组相比,部分肝切除术后 HS 组肝再生率和 BrdU 标记指数明显升高。与对照组相比,部分肝切除术后 HS 组血清和肝组织中的 IL6 和 TNFα 明显减少。Western blot 检测未发现信号转导和转录激活因子 3(STAT3)蛋白的磷酸化。与对照组相比,肝切除术后 HS 组核因子-白细胞介素-6(NF-IL6)和核因子-κB(NF-kB)的转录因子结合活性明显降低。
热休克预处理似乎可以减轻肝损伤并促进肝再生,因为 HSP70 可以减轻肝部分切除术后肝组织中的炎症反应,并上调肝再生,而无需白细胞介素 6 STAT 信号通路。