Kandori Hitoshi, Aoki Masami, Miyamoto Yumiko, Nakamura Sayuri, Kobayashi Ryosuke, Matsumoto Mitsuharu, Yokoyama Kotaro
Integrated Pathology, Frontier Technology, Integrated & Translational Science, Axcelead Drug Discovery Partners, Inc., 26-1 Muraoka-Higashi 2-chome, Fujisawa-shi, Kanagawa 251-0012, Japan.
Integrated Biology, Kidney/Liver Disease, Integrated & Translational Science, Axcelead Drug Discovery Partners, Inc., 26-1 Muraoka-Higashi 2-chome, Fujisawa-shi, Kanagawa 251-0012, Japan.
J Toxicol Pathol. 2024 Jan;37(1):29-37. doi: 10.1293/tox.2023-0053. Epub 2023 Oct 27.
This study was conducted to visualize the lobular distribution of enhanced mRNA expression levels of heat shock proteins (HSPs) in liver samples from carbon tetra chloride (CCl4)-treated mice using hybridization (ISH). Male BALB/c mice given a single oral administration of CCl4 were euthanized 6 hours or 1 day after the administration (6 h or 1 day). Paraffin-embedded liver samples were obtained, ISH for HSPs was conducted, as well as hematoxylin-eosin staining and immunohistochemistry (IHC). At 6 h, centrilobular hepatocellular vacuolization was observed, and increased signals for , and , which are HSPs, were noted in the centrilobular area using ISH. At 1 day, zonal hepatocellular necrosis was observed in the centrilobular area, but mRNA signal increases for HSPs were no longer observed there. Some discrepancies between ISH and IHC for HSPs were observed, and they might be partly caused by post-transcriptional gene regulation, including the ribosome quality control mechanisms. It is known that CCl4 damages centrilobular hepatocytes through metabolization by cytochrome P450, mainly located in the centrilobular region, and HSPs are induced under cellular stress. Therefore, our ISH results visualized increased mRNA expression levels of HSPs in the centrilobular hepatocytes of mice 6 hours after a single administration of CCl4 as a response to cellular stress, and it disappeared 1 day after the treatment when remarkable necrosis was observed there.
本研究旨在通过原位杂交(ISH)观察四氯化碳(CCl4)处理的小鼠肝脏样本中热休克蛋白(HSPs)增强的mRNA表达水平的小叶分布。单次口服给予CCl4的雄性BALB/c小鼠在给药后6小时或1天(6小时或1天)实施安乐死。获取石蜡包埋的肝脏样本,进行HSPs的原位杂交,以及苏木精-伊红染色和免疫组织化学(IHC)。在6小时时,观察到中央小叶肝细胞空泡化,并且使用原位杂交在中央小叶区域发现HSPs中的HSP25、HSP70和HSP90的信号增加。在1天时,在中央小叶区域观察到带状肝细胞坏死,但在那里不再观察到HSPs的mRNA信号增加。观察到HSPs的原位杂交和免疫组织化学之间存在一些差异,它们可能部分由转录后基因调控引起,包括核糖体质量控制机制。已知CCl4通过主要位于中央小叶区域的细胞色素P450代谢损害中央小叶肝细胞,并且HSPs在细胞应激下被诱导。因此,我们的原位杂交结果显示,单次给予CCl4后6小时,小鼠中央小叶肝细胞中HSPs的mRNA表达水平增加,作为对细胞应激的反应,并且在治疗1天后当在那里观察到明显坏死时消失。