Novel antibody to human BASP1 labels apoptotic cells post-caspase activation

被引:16
作者
Ohsawa, Shizue [1 ]
Watanabe, Tomomi [3 ,4 ]
Katada, Toshiaki [3 ]
Nishina, Hiroshi [4 ]
Miura, Masayuki [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Genet, Bunkyo Ku, Tokyo 1130033, Japan
[2] JST, CREST, Tokyo 1130033, Japan
[3] Univ Tokyo, Grad Sch Pharmaceut Sci, Dept Physiol Chem, Bunkyo Ku, Tokyo 1130033, Japan
[4] Tokyo Med & Dent Univ, Med Res Inst, Dept Dev & Regenerat Biol, Tokyo 1138510, Japan
基金
日本学术振兴会;
关键词
apoptosis; caspase; cell death-specific antibody; human BASP1;
D O I
10.1016/j.bbrc.2008.04.056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Apoptosis is associated with morphological changes, including membrane blebbing, cell shrinkage, and chromatin condensation. However, the molecular mechanisms of the dynamic changes in cellular components during apoptosis are largely unknown. Here we developed a new rat monoclonal antibody, 9B1, that specifically immunolabeled dying cells in tissues and in cell cultures. The 9B1 antibody labeled the cytoplasm of apoptotic cells in a caspase-dependent manner. We identified human brain abundant membrane attached signal protein 1 (hBASP1) as the 9B1 antigen using the liquid chromatography with tandem mass spectrometry (LC/MS/MS) method. hBASP1 was present in the nucleus of HeLa cells, but relocated from the nucleus to the cytoplasm after the caspase activation step of apoptosis. Immunostaining analysis revealed that 9B1 preferentially labeled this cytoplasmic form of hBASP1. Labeling by 9B1 to distinguish apoptotic changes could be a novel criterion for determining whether cells with activated caspases are fated for survival or death. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:639 / 643
页数:5
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