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G protein-coupled receptor crosstalk and signaling in hematopoietic stem and progenitor cells

机译:G蛋白偶联受体串扰和造血干细胞中的信号传导

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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 CysLT1 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:各种G蛋白偶联受体(GPCR)在造血干和祖细胞(HPC)中表达,包括趋化因子受体CXCR4,白酮受体CysLT1,鞘氨醇1-磷酸受体S1P1,大麻素受体CB2和补体受体C3AR。虽然CXCR4在茎细胞归巢中的作用在很大程度上建立,但仅部分地理解了HPC中表达的其他GPCR的功能。 CXCR4和CySLT1在配体结合后抑制自己的活化(同源脱敏)。已经显示S1P1或C3AR的刺激在HPC中激活CXCR4,其可以敏感CXCR4依赖性干细胞归巢。相比之下,CXCR4的激活导致Cyslt1功能的丧失,最可能由蛋白激酶C(PKC)信号传导(异源脱敏)介导,并且可以解释Cyslt1拮抗剂在体内动员HPC的无效性。 GPCR串扰的进一步表征将更好地了解HPC贩运。

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