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A/JCr小鼠中与肝螺杆菌持续感染相关的慢性增殖性肝炎:螺杆菌诱导致癌作用的模型

Chronic proliferative hepatitis in A/JCr mice associated with persistent Helicobacter hepaticus infection: a model of helicobacter-induced carcinogenesis.

作者信息

Fox J G, Li X, Yan L, Cahill R J, Hurley R, Lewis R, Murphy J C

机构信息

Division of Comparative Medicine, Massachusetts Institute of Technology, Cambridge, USA.

出版信息

Infect Immun. 1996 May;64(5):1548-58. doi: 10.1128/iai.64.5.1548-1558.1996.

Abstract

Helicobacter hepaticus causes hepatitis in selected strains of mice and in A/JCr mice is linked to liver cancer. To analyze whether H. hepaticus persists in specified ecological niches, to determine whether biomarkers of infection exist, and to analyze the influence of H. hepaticus on hepatocyte proliferation, a longitudinal study of H. hepaticus-infected A/JCr mice was undertaken. A/JCr mice were serially euthanatized from 3 through 18 months and surveyed by enzyme-linked immunosorbent assay; bacterial culture of liver, colon, and cecum; histology; electron microscopy; hepatocyte proliferation indices determined by using 5-bromo-2'-deoxyuridine; and measurement of the liver enzyme alanine aminotransferase. In infected animals throughout the 18-month study, H. hepaticus was consistently isolated from the lower bowel but only sporadically from the liver. By electron microscopy, H. hepaticus was noted infrequently and only in bile canaliculi. Infected mice, particularly males, showed chronic inflammation; oval cell, Kupffer cell, and Ito cell hyperplasia; hepatocytomegaly; and bile duct proliferation. The inflammatory and necrotizing lesion was progressive and involved the hepatic parenchyma, portal triads, and intralobular venules. Hepatic adenomas were noted only in male mice, whereas 5-bromo-2'-deoxyuridine proliferation indices were markedly increased in both sexes, but especially in males, compared to control A/J mice. Infected mice also developed sustained anti-H. hepaticus serum immunoglobulin G antibody responses and elevated alanine aminotransferase levels. H. hepaticus, which persists in the lower bowels and livers of A/JCr mice, is associated with a chronic proliferative hepatitis, and hepatomas in selected male mice indicate that this novel bacterium may cause an increased risk of hepatic cancer induction in susceptible strains of mice. This murine model should prove useful in dissecting the molecular events operable in the development of neoplasms induced by bacteria belonging to this expanding genera of pathogenic Helicobacter species.

摘要

肝螺杆菌可在特定品系小鼠中引发肝炎,在A/JCr小鼠中还与肝癌有关。为分析肝螺杆菌是否在特定生态位中持续存在,确定是否存在感染生物标志物,并分析肝螺杆菌对肝细胞增殖的影响,对感染肝螺杆菌的A/JCr小鼠进行了一项纵向研究。从3个月至18个月连续对A/JCr小鼠实施安乐死,并通过酶联免疫吸附测定、肝脏、结肠和盲肠的细菌培养、组织学、电子显微镜检查、使用5-溴-2'-脱氧尿苷测定肝细胞增殖指数以及测量肝酶丙氨酸氨基转移酶进行检测。在整个18个月的研究中,感染动物的肝螺杆菌始终能从下消化道分离得到,但仅偶尔能从肝脏分离到。通过电子显微镜观察,肝螺杆菌很少被发现,且仅在胆小管中出现。受感染的小鼠,尤其是雄性小鼠,表现出慢性炎症、卵圆细胞、库普弗细胞和伊托细胞增生、肝细胞肿大以及胆管增生。炎症和坏死性病变呈进行性发展,累及肝实质、门三联管和小叶内小静脉。仅在雄性小鼠中发现了肝腺瘤,而与对照A/J小鼠相比,两性的5-溴-2'-脱氧尿苷增殖指数均显著升高,但雄性更为明显。受感染的小鼠还产生了持续的抗肝螺杆菌血清免疫球蛋白G抗体反应以及丙氨酸氨基转移酶水平升高。肝螺杆菌在A/JCr小鼠的下消化道和肝脏中持续存在,与慢性增殖性肝炎有关,而特定雄性小鼠中的肝癌表明这种新型细菌可能会增加易感品系小鼠诱发肝癌的风险。这个小鼠模型在剖析由属于这一不断扩大的致病性螺杆菌属细菌诱导肿瘤发生过程中可操作的分子事件方面应会很有用。

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