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D(3) dopamine receptor activates phospholipase D through a pertussis toxin-insensitive pathway.

机译:D(3)多巴胺受体通过百日咳毒素不敏感途径激活磷脂酶D。

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摘要

Within the dopamine receptor family, the D(3) dopamine receptor's function remains inadequately described. The D(3) receptor has been shown to couple to inhibition of adenylyl cyclase, stimulation of mitogenesis, and regulation of K(+) and Ca(2+) currents, all in a pertussis toxin (PTX)-sensitive manner. Here we report D(3) receptor activation of the phospholipase D (PLD) enzyme in HEK 293 cells heterologously expressing the human D(3) receptor. Activation by agonist is dose dependent and displays the pharmacology expected of the D(3) receptor. The D(3) receptor specific antagonists AJ-76 and U99194A ablated the increase in activity by the preferring D(3) agonist (+) 7-OH DPAT. In addition, the D(3) receptor-mediated activation of PLD is not mediated by G-proteins of the G(i)/G(o) family, as pretreatment with PTX had no effect. PLD activation is a novel finding for the D(3) receptor, and is the first example of an effector system where D(3) signals without G(i)/G(o) protein intermediates.
机译:在多巴胺受体家族中,D(3)多巴胺受体的功能仍然没有充分描述。 D(3)受体已被证明对百日咳毒素(PTX)敏感的方式耦合到抑制腺苷酸环化酶,刺激有丝分裂以及调节K(+)和Ca(2+)电流。在这里我们报告异源表达人类D(3)受体的HEK 293细胞中的磷脂酶D(PLD)酶的D(3)受体激活。激动剂的激活是剂量依赖性的,并显示出预期的D(3)受体的药理作用。 D(3)受体特异性拮抗剂AJ-76和U99194A通过偏爱D(3)激动剂(+)7-OH DPAT消除了活性增加。此外,D(3)受体介导的PLD活化不受G(i)/ G(o)家族G蛋白的介导,因为PTX预处理无作用。 PLD激活是D(3)受体的新发现,并且是效应系统的第一个示例,其中D(3)信号不包含G(i)/ G(o)蛋白中间体。

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