Zlot C H, Flynn L M, Véniant M M, Kim E, Raabe M, McCormick S P, Ambroziak P, McEvoy L M, Young S G
Gladstone Institute of Cardiovascular Disease, San Francisco, CA 94141-9100, USA.
J Lipid Res. 1999 Jan;40(1):76-84.
Over the past 10 years, many laboratories have investigated lipid metabolism and atherogenesis with a variety of transgenic and gene knockout mouse models. Although many of these studies have yielded valuable insights, some have been hampered by a paucity of useful antibodies against mouse proteins. For example, many laboratories have analyzed genetic and dietary interventions affecting lipoprotein metabolism without useful antibodies against mouse apolipoprotein (apo) B. In this study, we sought to develop highly specific monoclonal antibodies against mouse apoB-100. To achieve this goal, gene-targeted mice that synthesize exclusively apoB-48 (apoB-48-only mice) were immunized with mouse apoB-100. The immune response against apoB-100 was robust, as judged by high titers of antibodies against mouse apoB-100. After fusing the splenic lymphocytes of the apoB-48-only mice with a myeloma cell line, we identified and cloned hybridomas that produced mouse apoB-100-specific monoclonal antibodies. Those antibodies were useful for developing sensitive and specific immunoassays for mouse apoB-100. This study illustrates the feasibility and utility of using gene-targeted mice to develop monoclonal antibodies against mouse proteins.
在过去10年里,许多实验室利用各种转基因和基因敲除小鼠模型研究了脂质代谢和动脉粥样硬化的发生机制。尽管其中许多研究都产生了有价值的见解,但有些研究因缺乏针对小鼠蛋白的有效抗体而受到阻碍。例如,许多实验室在没有针对小鼠载脂蛋白(apo)B的有效抗体的情况下,分析了影响脂蛋白代谢的遗传和饮食干预措施。在本研究中,我们试图开发针对小鼠apoB - 100的高度特异性单克隆抗体。为实现这一目标,用小鼠apoB - 100对仅合成apoB - 48的基因靶向小鼠(仅apoB - 48小鼠)进行免疫。从小鼠对apoB - 100的高滴度抗体判断,针对apoB - 100的免疫反应很强。将仅apoB - 48小鼠的脾淋巴细胞与骨髓瘤细胞系融合后,我们鉴定并克隆了产生小鼠apoB - 100特异性单克隆抗体的杂交瘤。这些抗体可用于开发针对小鼠apoB - 100的灵敏且特异的免疫测定方法。本研究说明了利用基因靶向小鼠开发针对小鼠蛋白的单克隆抗体的可行性和实用性。