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首页> 外文期刊>Annals of the New York Academy of Sciences >G protein-coupled receptor crosstalk and signaling in hematopoietic stem and progenitor cells
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G protein-coupled receptor crosstalk and signaling in hematopoietic stem and progenitor cells

机译:造血干细胞和祖细胞中的G蛋白偶联受体串扰和信号传导

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摘要

A variety of G protein-coupled receptors (GPCRs) is expressed in hematopoietic stem and progenitor cells (HPCs), including the chemokine receptor CXCR4, the leukotriene receptor CysLT1, the sphingosine 1-phosphate receptor S1P1, the cannabinoid receptor CB2, and the complement receptor C3aR. While the role of CXCR4 in stem cell homing is largely established, the function of the other GPCRs expressed in HPCs is only partially understood. CXCR4 and CysLTl inhibit their own activation after ligand binding (homologous desensitization). Stimulation of S1P1 or C3aR has been shown to activate CXCR4 in HPCs that may sensitize CXCR4-dependent stem cell homing. In contrast, activation of CXCR4 results in a loss of CysLT1 function, which is most likely mediated by protein kinase C (PKC) signaling (heterologous desensitization) and could explain the ineffectiveness of CysLT1 antagonists to mobilize HPCs in vivo. Further characterization of GPCR crosstalk will allow a better understanding of HPC trafficking.
机译:多种G蛋白偶联受体(GPCR)在造血干细胞和祖细胞(HPC)中表达,包括趋化因子受体CXCR4,白三烯受体CysLT1,鞘氨醇1磷酸鞘氨醇受体S1P1,大麻素受体CB2和补体。受体C3aR。尽管在很大程度上确定了CXCR4在干细胞归巢中的作用,但仅部分了解了HPC中表达的其他GPCR的功能。在配体结合后(同源脱敏),CXCR4和CysLT1抑制其自身的活化。 S1P1或C3aR的刺激已显示可激活HPC中的CXCR4,这可能会使CXCR4依赖性干细胞归巢敏感。相反,CXCR4的激活导致CysLT1功能的丧失,这很可能是由蛋白激酶C(PKC)信号传导(异源脱敏)介导的,并且可以解释CysLT1拮抗剂在体内动员HPC的有效性。 GPCR串扰的进一步表征将有助于更好地了解HPC交易。

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