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肥大细胞中催产素受体和5-羟色胺转运体的特性分析

Characterization of oxytocin receptors and serotonin transporters in mast cells.

作者信息

Vega Edgardo, Rudolph Maria Isolde

机构信息

Department of Pharmacology, Facultad de Ciencias Biológicas, Universidad de Concepción, Chile.

出版信息

Endocrine. 2002 Jul;18(2):167-72. doi: 10.1385/ENDO:18:2:167.

Abstract

Oxytocin (OT) inhibits the uptake of serotonin (5HT) into uterine mast cells. This may modulate 5HT bioavailability in the myometrium. Because 5HT isan important endogenous uterotonic compound, it has been postulated that this effect of OT may contribute to its potency as a labor inducer. This also predicts the presence of oxytocin receptors (OTRs) and transducing signals that will interact with 5HT transporters (SERT) in mast cells. In this study, OTR and SERT were characterized in murine peritoneal mast cells by radioligand-binding studies. Saturation assays for OTR showed no changes in Kd along the estrous cycle (6.95 +/- 2.76 nM in estrus and 4.07 +/- 1.73 nM in diestrus) but an increase in Bmax in estrus (0.71 +/- 0.08 pmol/10(6) cells and 0.37 +/- 0.05 pmol/10(6) cells in estrus and diestrus, respectively). Bmax and Kd for SERT were not affected along the estrous cycle. The signaling between the OTR and the SERT was analyzed by measuring the extent of inhibition of OT and PMA (activator of protein kinase C on 5HT uptake and the capability of Ro318220 (specific inhibitor of PKC) to increase 5HT uptake and block the effect of the above compounds in mast cells. The results showed that in murine peritoneal mast cells in vitro (1) ovarian hormones modulate OTR but not SERT expression, (2) the magnitude of OT action on 5HT uptake depends on the number of OTRs expressed in mast cells, and (3) the signaling between OTR and the SERT is mediated through the activation of protein kinase C. It is concluded that the ovarian hormones have a modulatory action on 5HT uptake which involves OT-mediated mechanism.

摘要

催产素(OT)可抑制子宫肥大细胞对血清素(5HT)的摄取。这可能会调节子宫肌层中5HT的生物利用度。由于5HT是一种重要的内源性子宫收缩化合物,因此推测OT的这种作用可能有助于其作为引产剂的效力。这也预示着催产素受体(OTRs)的存在以及将与肥大细胞中的5HT转运体(SERT)相互作用的转导信号。在本研究中,通过放射性配体结合研究对小鼠腹膜肥大细胞中的OTR和SERT进行了表征。OTR的饱和分析显示,在发情周期中Kd没有变化(发情期为6.95±2.76 nM,动情间期为4.07±1.73 nM),但发情期的Bmax增加(发情期和动情间期分别为0.71±0.08 pmol/10⁶细胞和0.37±0.05 pmol/10⁶细胞)。SERT的Bmax和Kd在发情周期中不受影响。通过测量OT和PMA(蛋白激酶C激活剂)对5HT摄取的抑制程度以及Ro318220(PKC特异性抑制剂)增加5HT摄取并阻断上述化合物在肥大细胞中作用的能力,分析了OTR和SERT之间的信号传导。结果表明,在体外小鼠腹膜肥大细胞中:(1)卵巢激素调节OTR而非SERT的表达;(2)OT对5HT摄取的作用强度取决于肥大细胞中表达的OTR数量;(3)OTR和SERT之间的信号传导是通过蛋白激酶C的激活介导的。得出的结论是,卵巢激素对5HT摄取具有调节作用,这涉及OT介导的机制。

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