Lee Ju Yup, Kim Nayoung, Choi Yoon Jeong, Nam Ryoung Hee, Choi Yoon Jin, Kwon Yong Hwan, Yoon Kichul, Suh Ji Hyung, Lee Seon Min, Lee Hye Seung, Lee Dong Ho
Departments of Internal Medicine, Seoul National University Bundang Hospital, Seoungnam, Korea.
Pathology, Seoul National University Bundang Hospital, Seoungnam, Korea.
J Cancer Prev. 2014 Sep;19(3):224-30. doi: 10.15430/JCP.2014.19.3.224.
The Helicobacter felis (H. felis) mouse model has been developed for the research regarding pathogenesis of chronic gastritis and gastric cancer. The aim of this study was to investigate long-term H. felis colonization in the stomachs of C57BL/6 mice and subsequent histologic findings and inflammatory reactions including pro-inflammatory cytokines.
Twenty-three female C57BL/6 mice at 4 weeks of age were gavaged with H. felis, and 13 control mice served as vehicle only. The mice were sacrificed at 4, 24, and 52 weeks after inoculation. The infection status and degree of inflammation were determined by culture and histopathology. The level of gastric mucosal myeloperoxidase (MPO), tumor necrosis factor alpha (TNF-α), and interleukin-1beta (IL-1β) were measured by ELISA.
The overall infection rate was 100%, as determined by the culture and histology. At 4, 24, and 52 weeks, the neutrophil and monocyte scores were significantly higher in infected mice than in control mice. At 24 weeks after inoculation, most of the infected mice showed mucosal atrophy with or without metaplasia, and a few showed focal dysplasia. Adenocarcinoma was observed in one mouse at 52 week post-infection. Gastric mucosal MPO and IL-1β levels were significantly higher in infected mice than those in control mice at 24 and 52 weeks. However, the expression of gastric mucosal TNF-α was not significantly different between the infected and control mice at any time-point.
Long-term H. felis-infection in C57BL/6 mice provoked a severe inflammatory reaction and it progressed into atrophy, metaplasia, dysplasia and cancer. IL-1β might play an important role in the inflammatory response of mice to Helicobacter species.
幽门螺杆菌(H. felis)小鼠模型已被用于慢性胃炎和胃癌发病机制的研究。本研究的目的是调查幽门螺杆菌在C57BL/6小鼠胃内的长期定植情况以及随后的组织学发现和炎症反应,包括促炎细胞因子。
23只4周龄的雌性C57BL/6小鼠经口灌胃感染幽门螺杆菌,13只对照小鼠仅给予溶剂。在接种后4周、24周和52周处死小鼠。通过培养和组织病理学确定感染状态和炎症程度。采用酶联免疫吸附测定法(ELISA)检测胃黏膜髓过氧化物酶(MPO)、肿瘤坏死因子α(TNF-α)和白细胞介素-1β(IL-1β)水平。
通过培养和组织学检查确定总体感染率为100%。在4周、24周和52周时,感染小鼠的中性粒细胞和单核细胞评分显著高于对照小鼠。接种后24周,大多数感染小鼠出现黏膜萎缩,伴有或不伴有化生,少数出现局灶性发育异常。感染后52周在1只小鼠中观察到腺癌。在24周和52周时,感染小鼠的胃黏膜MPO和IL-1β水平显著高于对照小鼠。然而在任何时间点,感染小鼠和对照小鼠胃黏膜TNF-α的表达均无显著差异。
C57BL/6小鼠长期感染幽门螺杆菌引发了严重的炎症反应,并进展为萎缩、化生、发育异常和癌症。IL-1β可能在小鼠对幽门螺杆菌的炎症反应中起重要作用。