Rajashekhar Gangaraju, Mitnacht-Kraus Rita, Ispe Ute, Garrison Jana, Hou Yonghao, Taylor Brian, Petrache Irina, Vestweber Dietmar, Clauss Matthias
Department of Cellular and Integrative Physiology, Indiana Center for Vascular Biology & Medicine, IU School of Medicine, Indianapolis, IN 46202, USA.
J Immunol Methods. 2009 Oct 31;350(1-2):22-8. doi: 10.1016/j.jim.2009.08.003. Epub 2009 Aug 14.
EMAP II is an endothelial cell and monocyte activating proinflammatory cytokine, which has been demonstrated to induce endothelial cell apoptosis. In order to analyze its role in disease models linked to inflammation and endothelial cell death, we aimed to develop a neutralizing antibody against mouse EMAP II. Therefore, we generated rat monoclonal anti-mouse EMAP II antibodies by immunization with recombinant full length, mouse pro-EMAP II protein. We could identify by ELISA, hybridoma clones from fusion with mouse myeloma SP2/0 cells which produced antibodies recognizing both full length and mature EMAP II. We further characterized one antibody, M7/1 and demonstrated its ability to detect both EMAP II forms in Western blotting and to neutralize EMAP II directed migration of human peripheral blood monocytes as well as EMAP II induced apoptosis of tumor and endothelial cells. We conclude that this antibody can be useful to both target and analyze murine disease models, in which EMAP II may be involved.
内皮单核细胞激活肽II(EMAP II)是一种可激活内皮细胞和单核细胞的促炎细胞因子,已被证明可诱导内皮细胞凋亡。为了分析其在与炎症和内皮细胞死亡相关的疾病模型中的作用,我们旨在开发一种抗小鼠EMAP II的中和抗体。因此,我们用重组全长小鼠前EMAP II蛋白进行免疫,制备了大鼠抗小鼠EMAP II单克隆抗体。通过酶联免疫吸附测定(ELISA),我们从与小鼠骨髓瘤SP2/0细胞融合产生的杂交瘤克隆中,鉴定出能识别全长和成熟EMAP II的抗体。我们进一步对一种名为M7/1的抗体进行了特性分析,证明它在蛋白质免疫印迹法中能检测到两种形式的EMAP II,并能中和EMAP II介导的人外周血单核细胞迁移以及EMAP II诱导的肿瘤细胞和内皮细胞凋亡。我们得出结论,这种抗体可用于靶向和分析可能涉及EMAP II的小鼠疾病模型。