Department of Molecular Pharmacology and Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Sendai, Japan.
Monoclon Antib Immunodiagn Immunother. 2022 Jun;41(3):133-141. doi: 10.1089/mab.2022.0010.
The CXC chemokine receptor 6 (CXCR6) is a member of the G protein-coupled receptor family that is highly expressed in helper T type 1 cells, natural killer cells, cytotoxic T lymphocytes, and various type of cells in tumor microenvironment (TME). CXCR6 has been proposed as a therapeutic target against tumors through regulation of the tumor TME. In this study, we developed specific and sensitive monoclonal antibodies (mAbs) for mouse CXCR6 (mCXCR6), which are useful for flow cytometry and Western blotting by N-terminal peptide immunization into rat. The established anti-mCXCR6 mAb, CxMab-1 (rat IgG, kappa), reacted with not only mCXCR6-overexpressed Chinese hamster ovary-K1 (CHO/mCXCR6) but also mCXCR6-endogenously expressed cell lines, such as P388 (mouse lymphoid neoplasm) and J774-1 (mouse macrophage-like) through flow cytometry. Kinetic analyses using flow cytometry indicated that the dissociation constants () of CxMab-1 for CHO/mCXCR6, P388, and J774-1 cells were 1.7 × 10 M, 3.4 × 10 M, and 3.8 × 10 M, respectively. Furthermore, CxMab-1 could detect endogenous mCXCR6 in P388 and J774-1 cells by Western blotting. These results indicated that CxMab-1 is useful for detecting mCXCR6 by flow cytometry and Western blotting, and provides a possibility for targeting CXCR6-expressing cells experiments.
CXC 趋化因子受体 6(CXCR6)是 G 蛋白偶联受体家族的成员,在辅助性 T 细胞 1 型、自然杀伤细胞、细胞毒性 T 淋巴细胞和肿瘤微环境(TME)中的各种类型的细胞中高度表达。CXCR6 已被提议通过调节肿瘤 TME 作为抗肿瘤的治疗靶点。在这项研究中,我们通过对大鼠进行 N 端肽免疫,开发了用于流式细胞术和 Western blot 的针对小鼠 CXCR6(mCXCR6)的特异性和灵敏性单克隆抗体(mAbs)。建立的抗 mCXCR6 mAb,CxMab-1(大鼠 IgG,kappa),不仅与过表达 mCXCR6 的中国仓鼠卵巢-K1(CHO/mCXCR6)反应,而且与 mCXCR6 内源性表达的细胞系,如 P388(小鼠淋巴样肿瘤)和 J774-1(小鼠巨噬细胞样)通过流式细胞术反应。使用流式细胞术进行的动力学分析表明,CxMab-1 与 CHO/mCXCR6、P388 和 J774-1 细胞的解离常数()分别为 1.7×10^-8 M、3.4×10^-8 M 和 3.8×10^-8 M。此外,CxMab-1 可以通过 Western blot 检测 P388 和 J774-1 细胞中的内源性 mCXCR6。这些结果表明,CxMab-1 可用于通过流式细胞术和 Western blot 检测 mCXCR6,并为靶向 CXCR6 表达细胞的实验提供了可能性。