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Identification of RANTES receptors on human monocytic cells: competition for binding and desensitization by homologous chemotactic cytokines

机译:人单核细胞上RANTES受体的鉴定:同源趋化细胞因子竞争结合和脱敏

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摘要

RANTES (regulated on activation, normal T expressed and secreted) is a member of the chemotactic cytokine (chemokine) beta subfamily. High affinity receptors for RANTES have been identified on a human monocytic leukemia cell line THP-1, which responded to RANTES in chemotaxis and calcium mobilization assays. Steady-state binding data analyses revealed approximately 700 binding sites/cell on THP-1 cells with a Kd value of 400 pM, comparable to that expressed on human peripheral blood monocytes. The RANTES binding to monocytic cells was competed for by monocyte chemotactic and activating factor (MCAF) and macrophage inflammatory protein 1 (MIP-1) alpha, two other chemokine beta cytokines. Although MCAF and MIP-1 alpha competed for RANTES binding to monocytes with apparent lower affinity (with estimated Kd of 6 and 1.6, nM respectively) both of these cytokines effectively desensitized the calcium mobilization induced by RANTES. The chemotactic response of THP- 1 cells to RANTES was also markedly inhibited by preincubation with MCAF or MIP-1 alpha. In contrast, RANTES did not desensitize the THP-1 calcium mobilization and chemotaxis in response to MCAF or MIP-1 alpha. These results, together with our previous observations that RANTES did not compete for MCAF or MIP-1 alpha binding on monocytic cells, indicate the expression of promiscuous receptors on monocytes that recognize one or more cytokines within the chemokine beta family.
机译:RANTES(受激活,正常T表达和分泌的调节)是趋化细胞因子(趋化因子)β亚家族的成员。在人单核细胞白血病细胞系THP-1上已鉴定出RANTES的高亲和力受体,该细胞系在趋化性和钙动员试验中对RANTES产生反应。稳态结合数据分析显示,THP-1细胞上约700个结合位点/细胞,Kd值为400 pM,与人外周血单核细胞上表达的Kd值相当。与单核细胞结合的RANTES由单核细胞趋化和激活因子(MCAF)和巨噬细胞炎性蛋白1(MIP-1)α(其他两种趋化因子β细胞因子)竞争。尽管MCAF和MIP-1α以明显较低的亲和力竞争RANTES与单核细胞的结合(估计Kd分别为6和1.6,nM),这两种细胞因子均有效地降低了RANTES诱导的钙动员。通过与MCAF或MIP-1α的预温育,THP-1细胞对RANTES的趋化反应也被显着抑制。相比之下,RANTES不会降低对MCAF或MIP-1α的THP-1钙动员和趋化性的敏感性。这些结果,加上我们先前的观察,即RANTES不竞争单核细胞上的MCAF或MIP-1 alpha结合,表明单核细胞上的混杂受体表达,这些受体识别趋化因子beta家族中的一种或多种细胞因子。

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