Varona R, Zaballos A, Gutiérrez J, Martín P, Roncal F, Albar J P, Ardavín C, Márquez G
Departamento de Immunología y Onocología, Centro Nacional de Biotecnología, Universidad Autónoma de Madrid, Cantoblanco, Spain.
FEBS Lett. 1998 Nov 27;440(1-2):188-94. doi: 10.1016/s0014-5793(98)01450-1.
We have cloned the murine CCR6 receptor and its ligand, the beta-chemokine mMIP-3alpha. Calcium mobilization assays performed with mCCR6 transfectants showed significant responses upon addition of mMIP-3alpha. Murine MIP-3alpha RNA is expressed in thymus, small intestine and colon, whereas mCCR6 RNA is expressed in spleen and lymph nodes. RT-PCR analysis of FACS-sorted lymphoid and antigen presenting cell subsets showed mCCR6 expression mainly in B cells, CD8- splenic dendritic cells and CD4+ T cells. The cloning and functional characterization of the mCCR6 and mMIP-3alpha will allow the study of the role of these proteins in mouse models of inflammation and immunity.
我们已经克隆了小鼠CCR6受体及其配体β-趋化因子mMIP-3α。用mCCR6转染子进行的钙动员试验表明,加入mMIP-3α后有显著反应。小鼠MIP-3αRNA在胸腺、小肠和结肠中表达,而mCCR6 RNA在脾脏和淋巴结中表达。对通过荧光激活细胞分选术分选的淋巴细胞和抗原呈递细胞亚群进行逆转录聚合酶链反应分析表明,mCCR6主要在B细胞、脾脏CD8-树突状细胞和CD4+T细胞中表达。mCCR6和mMIP-3α的克隆及功能特性研究将有助于探讨这些蛋白质在小鼠炎症和免疫模型中的作用。