Toyonaga T, Hino O, Sugai S, Wakasugi S, Abe K, Shichiri M, Yamamura K
Department of Developmental Genetics, Kumamoto University School of Medicine, Japan.
Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):614-8. doi: 10.1073/pnas.91.2.614.
Interferon-gamma may play an important role in the immune response and in inflammatory diseases, including chronic active hepatitis. To understand the role of interferon-gamma in the regulation of inflammation and to establish a mouse model of chronic active hepatitis, we produced transgenic mice in which the mouse interferon-gamma gene was regulated by a liver-specific promoter, the serum amyloid P component gene promoter. Four transgenic mouse lines were generated, and two of these lines expressed mRNA of interferon-gamma in the liver. Levels of serum transaminases increased gradually as a function of age and were significantly higher than those of interferon-gamma-negative littermates after 4 weeks after birth. One transgenic mouse line showed a histology of chronic active hepatitis similar to that found in human patients, although cirrhotic changes such as fibrosis were scarce. Thus, the liver-specific production of interferon-gamma is sufficient to induce chronic inflammatory disease and this mouse is a transgenic model of chronic active hepatitis.
干扰素-γ可能在免疫反应以及包括慢性活动性肝炎在内的炎症性疾病中发挥重要作用。为了了解干扰素-γ在炎症调节中的作用并建立慢性活动性肝炎小鼠模型,我们制备了转基因小鼠,其中小鼠干扰素-γ基因由肝脏特异性启动子——血清淀粉样P成分基因启动子调控。产生了四个转基因小鼠品系,其中两个品系在肝脏中表达干扰素-γ的mRNA。血清转氨酶水平随年龄增长逐渐升高,出生后4周时显著高于干扰素-γ阴性的同窝小鼠。一个转基因小鼠品系表现出与人类患者相似的慢性活动性肝炎组织学特征,尽管诸如纤维化等肝硬化改变很少见。因此,肝脏特异性产生干扰素-γ足以诱发慢性炎症性疾病,并且这种小鼠是慢性活动性肝炎的转基因模型。