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Expression of interleukin 6 and apoptosis-related genes in suckling and weaning rat models of hepatectomy and liver regeneration.

机译:白细胞介素6和凋亡相关基因在乳,断奶大鼠肝切除和肝再生模型中的表达。

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摘要

BACKGROUND/PURPOSE: The most commonly used model to study the mechanisms of liver regeneration is the adult rat submitted to 70% to 80% hepatectomy. However, there are no studies using newborn or weaning rat models. The process of liver regeneration includes both the hypertrophy and hyperplasia of cells (processes regulated by growth factors and cytokines, mainly interleukin 6 [IL-6]) as well as apoptosis, or programmed cell death (a process regulated mainly by the Bcl-2 family of proteins). Proapoptotic proteins in this family include Bax and Bak. Conversely, Bcl-2 and Bcl-XL are antiapoptotic regulators. Therefore, to expand our understanding of liver regeneration, our study had 2 goals: first, to standardize 2 animal models of hepatectomy and liver regeneration using the newborn suckling and the weaning rat and second, to quantitate the expression levels of IL-6 and several members of the Bcl-2 gene family during the regeneration process. METHODS: To create the experimental models, newborn suckling rats (age, 5-7 days; weight, 6-10 g) and weaning rats (age, 21-23 days; weight, 30-50 g) underwent 70% hepatectomy. The animals were subsequently sacrificed at days 1, 2, 3, 4, and 7 after hepatectomy, and the remnant liver lobes were harvested for routine histologic examination. Groups of healthy animals not operated on served as controls. For the experimental study, 6 newborn rats and 6 weaning rats underwent hepatectomy. The animals were killed 1 day after liver resection and the remnant livers were harvested to assess gene expression by quantitative reverse transcription-polymerase chain reaction. The hepatectomized groups were compared with control and sham groups. RESULTS: During the creation of the experimental models, 70% of the suckling animals and all the weaning animals survived the hepatectomy. The decreased liver weight was completely restored to control levels by day 7 after hepatectomy. Histologically, the remnant livers of both hepatectomy groups exhibited steatosis, tumefaction of hepatocytes, and mitosis, which ceased at 7 days after the hepatectomy. The weaning rat model showed more robust gene expression responses. Specifically, expression levels of IL-6 gene were significantly increased after both surgical insult (sham group) and hepatectomy. However, this increase was significantly higher in the latter group. Furthermore, hepatectomy promoted a decrease in the expression levels of the proapoptotic genes and an increase in the expression levels of Bcl-2. CONCLUSIONS: Our data indicate that regulation of both IL-6 and genes involved in apoptosis are strongly implicated in the mechanisms of liver regeneration and that the weaning rat model represents an attractive model system for future investigations in this area.
机译:背景/目的:研究肝再生机制最常用的模型是接受70%至80%肝切除的成年大鼠。但是,尚无使用新生或断奶大鼠模型的研究。肝再生的过程包括细胞的肥大和增生(受生长因子和细胞因子调节的过程,主要是白介素6 [IL-6])以及细胞凋亡或程序性细胞死亡(主要受Bcl-2调节的过程)蛋白质家族)。该家族中的凋亡蛋白包括Bax和Bak。相反,Bcl-2和Bcl-XL是抗凋亡调节剂。因此,为了扩大我们对肝脏再生的理解,我们的研究有两个目标:首先,使用新生的乳头和断奶的大鼠标准化两种肝切除和肝脏再生的动物模型;其次,量化IL-6的表达水平和几种再生过程中Bcl-2基因家族的成员。方法:为建立实验模型,对新生的乳鼠(年龄5-7天;体重6-10 g)和断奶大鼠(年龄21-23天;体重30-50 g)进行70%肝切除术。随后在肝切除后的第1、2、3、4和7天处死动物,并收集残余的肝叶用于常规组织学检查。未进行手术的健康动物组作为对照。为了进行实验研究,对6只新生大鼠和6只断奶大鼠进行了肝切除术。肝脏切除后1天将动物处死,并通过定量逆转录-聚合酶链反应收集残余肝脏以评估基因表达。将肝切除组与对照组和假组进行比较。结果:在创建实验模型的过程中,有70%的哺乳动物和所有断奶动物都存活了肝切除术。肝切除后第7天,肝脏重量的减少已完全恢复到控制水平。从组织学上看,两组肝切除术后的残余肝均表现出脂肪变性,肝细胞肿瘤和有丝分裂,这些在肝切除术后第7天停止。断奶的大鼠模型显示出更强大的基因表达反应。具体而言,在手术损伤(假手术组)和肝切除术之后,IL-6基因的表达水平显着增加。但是,后者组的这种增加明显更高。此外,肝切除术促进促凋亡基因的表达水平降低和Bcl-2表达水平的升高。结论:我们的数据表明,IL-6和细胞凋亡相关基因的调节与肝再生机制密切相关,断奶大鼠模型代表了该领域未来研究的有吸引力的模型系统。

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