Wilson S P
Department of Pharmacology, USC School of Medicine, Columbia 29208.
J Neurochem. 1993 Nov;61(5):1901-6. doi: 10.1111/j.1471-4159.1993.tb09832.x.
The synthesis of the neuropeptide precursor proenkephalin was measured in bovine adrenal chromaffin cells following radiolabeling with [35S]methionine. Treatment of chromaffin cells with pertussis toxin (100 ng/ml) approximately doubled proenkephalin synthesis without altering total protein synthesis. Pertussis toxin pretreatment also increased proenkephalin synthesis in chromaffin cells exposed to vasoactive intestinal peptide (VIP) and 3-isobutyl-1-methylxanthine (IBMX). Combinations of IBMX plus nicotine, VIP, or histamine also synergistically enhanced proenkephalin synthesis, with no further elevation when the cells were also pretreated with pertussis toxin. The action of forskolin, a direct activator of adenylate cyclase, on proenkephalin synthesis was similarly potentiated by pertussis toxin or IBMX, presumably reflecting the abilities of both the toxin and this phosphodiesterase inhibitor to enhance the cyclic AMP response to forskolin. In contrast, increased synthesis of proenkephalin in response to phorbol esters was not affected by pertussis toxin treatment. These results suggest that pertussis toxin potentiates proenkephalin synthesis primarily through inactivation of guanine nucleotide-binding proteins that inhibit adenylate cyclase, although other signaling pathways may also be involved.
在用[35S]甲硫氨酸进行放射性标记后,测定了牛肾上腺嗜铬细胞中神经肽前体脑啡肽原的合成。用百日咳毒素(100 ng/ml)处理嗜铬细胞,脑啡肽原合成增加了约一倍,而总蛋白合成未改变。百日咳毒素预处理还增加了暴露于血管活性肠肽(VIP)和3-异丁基-1-甲基黄嘌呤(IBMX)的嗜铬细胞中脑啡肽原的合成。IBMX与尼古丁、VIP或组胺的组合也协同增强了脑啡肽原的合成,当细胞也用百日咳毒素预处理时,没有进一步升高。腺苷酸环化酶的直接激活剂福斯高林对脑啡肽原合成的作用同样被百日咳毒素或IBMX增强,这大概反映了毒素和这种磷酸二酯酶抑制剂增强对福斯高林的环磷酸腺苷反应的能力。相反,佛波酯诱导的脑啡肽原合成增加不受百日咳毒素处理的影响。这些结果表明,百日咳毒素主要通过使抑制腺苷酸环化酶的鸟苷酸结合蛋白失活来增强脑啡肽原的合成,尽管其他信号通路可能也参与其中。