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由肝螺杆菌引起的小鼠慢性活动性肝炎。

Chronic active hepatitis in mice caused by Helicobacter hepaticus.

作者信息

Ward J M, Anver M R, Haines D C, Benveniste R E

机构信息

Veterinary and Tumor-Pathology Section, National Cancer Institute, NCI-Frederick Cancer Research, Maryland 21702-1201.

出版信息

Am J Pathol. 1994 Oct;145(4):959-68.

Abstract

Helicobacter infections cause chronic gastroenteritis in humans and several animal species. We recently discovered a new Helicobacter (H. hepaticus) that is the etiological agent of a unique chronic active hepatitis in mice. Natural infection appeared to be acquired early in life in enzootically infected colonies. Liver lesions arose as focal necrosis and focal nonsuppurative inflammation by 1 to 4 months of age in susceptible mouse strains. By 6 to 8 months, extensive liver involvement included hepatocytomegaly, bile ductular (oval cell) hyperplasia, and cholangitis. There was an age-related increase in proliferating cell nuclear antigen hepatocyte nuclear labeling index. The bacteria were usually found within bile canaliculi as determined by ultrastructural evaluation of liver lesions, the Steiner modification of the Warthin-Starry stain and immunohistochemistry with a rabbit antibody to Helicobacter pylori. Naturally infected mice showed an age-related increase in serum IgG antibodies to Helicobacter hepaticus proteins. The disease was experimentally reproduced by intraperitoneal injection of liver suspensions from affected livers or bacteria cultivated in vitro. The earliest lesions of the experimental disease appeared 4 weeks after injection. The course of spontaneous and experimental infection was slow and insidious and resulted in high titers of antibodies to bacterial proteins. This chronic bacterial infection represents a new model of chronic liver disease.

摘要

幽门螺杆菌感染可导致人类和多种动物患上慢性肠胃炎。我们最近发现了一种新的幽门螺杆菌(肝螺杆菌),它是小鼠独特的慢性活动性肝炎的病原体。在自然感染的种群中,自然感染似乎在生命早期就已发生。在易感小鼠品系中,1至4月龄时肝脏病变表现为局灶性坏死和局灶性非化脓性炎症。到6至8个月时,广泛的肝脏受累包括肝细胞肿大、胆管(卵圆细胞)增生和胆管炎。增殖细胞核抗原肝细胞核标记指数随年龄增长而增加。通过对肝脏病变的超微结构评估、Warthin-Starry染色的Steiner改良法以及使用抗幽门螺杆菌兔抗体进行免疫组织化学检测,发现细菌通常存在于胆小管内。自然感染小鼠血清中针对肝螺杆菌蛋白的IgG抗体随年龄增长而增加。通过腹腔注射来自患病肝脏的肝悬液或体外培养的细菌,可在实验中重现该疾病。实验性疾病最早在注射后4周出现。自发感染和实验性感染的病程缓慢且隐匿,并导致针对细菌蛋白的高滴度抗体产生。这种慢性细菌感染代表了一种新的慢性肝病模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f021/1887338/8f19445efae4/amjpathol00058-0218-a.jpg

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