首页> 外文期刊>Journal of Leukocyte Biology: An Official Publication of the Reticuloendothelial Society >Cloning and functional expression of CC CKR5, a human monocyte CC chemokine receptor selective for MIP-1(alpha), MIP-1(beta), and RANTES.
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Cloning and functional expression of CC CKR5, a human monocyte CC chemokine receptor selective for MIP-1(alpha), MIP-1(beta), and RANTES.

机译:CC CKR5的克隆和功能表达,CC CKR5是对MIP-1α,MIP-1β和RANTES具有选择性的人单核细胞CC趋化因子受体。

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We have cloned a human cDNA for a novel CC chemokine receptor (CC CKR) designated CC CKR5 that has 48-75% amino acid identity to other CC CKRs. CC CKR5 mRNA was detected constitutively in primary adherent monocytes but not in primary neutrophils or eosinophils. Macrophage inflammatory protein-1alpha (MIP-1alpha), MIP-1beta, and RANTES were all potent agonists for CC CKR5 (EC50 = 3-30 nM) when calcium flux was measured in transfected HEK 293 cells, yet the apparent binding affinities of the corresponding iodinated chemokines to intact cells expressing the receptor were low (IC50 approximately 100 nM). The calcium flux responses were completely blocked by treatment of transfected cells with pertussis toxin. These data suggest that CC CKR5 is a G(i)-coupled receptor that may mediate monocyte responses to MIP-1alpha, MIP-1beta, and RANTES.
机译:我们已经为新型CC趋化因子受体(CC CKR)克隆了人cDNA,命名为CC CKR5,它与其他CC CKR具有48-75%的氨基酸同一性。在原代贴壁单核细胞中组成性检测到CC CKR5 mRNA,但在原代中性粒细胞或嗜酸性粒细胞中未检测到。当在转染的HEK 293细胞中测量钙通量时,巨噬细胞炎性蛋白1alpha(MIP-1alpha),MIP-1beta和RANTES都是CC CKR5(EC50 = 3-30 nM)的有效激动剂,但它们的表观结合亲和力完整的表达受体的细胞对应的碘化趋化因子很低(IC50约为100 nM)。通过用百日咳毒素处理转染的细胞可以完全阻断钙通量反应。这些数据表明CC CKR5是G(i)耦合的受体,可以介导对MIP-1alpha,MIP-1beta和RANTES的单核细胞应答。

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