Jung Kyeong Cheon, Park Weon Seo, Kim Hae Jung, Choi Eun Young, Kook Myeong-Cherl, Lee Han-Woong, Bae Youngmee
Department of Pathology, Hallym University College of Medicine, Chuncheon, Korea.
J Immunol. 2004 Jan 15;172(2):795-802. doi: 10.4049/jimmunol.172.2.795.
CD24, also referred to as the heat-stable Ag, is a T cell differentiation Ag that is highly expressed on both CD4-CD8- double negative and CD4+CD8+ double positive thymocytes. Here, we report that CD24 ligation by a new anti-CD24 Ab, mT-20, induced the apoptosis of both double negative and double positive thymocytes, as well as the Scid.adh thymic lymphoma cell line, in the absence of TCR/CD3 engagement. CD24-mediated apoptosis of mouse thymocytes and its signaling pathway appeared not to be associated with p53, CD95, TNFR, or caspases. Furthermore, we found that cell death was blocked by the addition of scavengers of reactive oxygen species or by Bcl-2 overexpression, implying the role of CD24 signaling in the mitochondrial regulation. In this study, we suggest that CD24 ligation induced the apoptosis of immature thymocytes independently of both caspase and TCR.
CD24,也被称为热稳定抗原,是一种T细胞分化抗原,在CD4-CD8-双阴性和CD4+CD8+双阳性胸腺细胞上均高表达。在此,我们报道一种新的抗CD24抗体mT-20对CD24的连接在没有TCR/CD3参与的情况下诱导了双阴性和双阳性胸腺细胞以及Scid.adh胸腺淋巴瘤细胞系的凋亡。CD24介导的小鼠胸腺细胞凋亡及其信号通路似乎与p53、CD95、TNFR或半胱天冬酶无关。此外,我们发现通过添加活性氧清除剂或Bcl-2过表达可阻断细胞死亡,这意味着CD24信号在线粒体调节中的作用。在本研究中,我们认为CD24连接独立于半胱天冬酶和TCR诱导未成熟胸腺细胞凋亡。