Mitchell F M, Buckley N J, Milligan G
Department of Biochemistry, University of Glasgow, Scotland, U.K.
Biochem J. 1993 Jul 15;293 ( Pt 2)(Pt 2):495-9. doi: 10.1042/bj2930495.
Treatment of CHO cells stably expressing the human M1 muscarinic acetylcholine (HM1) receptor with the cholinergic agonist carbachol results in a reduction in cellular levels of Gq alpha/G11 alpha. Half-maximal effects are produced by 3 h, and a new steady state of some 50% of the resting levels of Gq alpha/G11 alpha is subsequently established [Mullaney, Dodd, Buckley and Milligan, (1993) Biochem. J. 289, 125-131]. To analyse the mechanism of this effect, we examined the rate of turnover of Gq alpha/G11 alpha in these HM1-expressing cells in the presence and absence of carbachol (1 mM). In untreated cells the measured removal of 35S-labelled Gq alpha/G11 alpha was adequately described by a monoexponential curve with a half-time (t0.5) of 18.0 +/- 2.2 h. When the cells were treated with carbachol a more complex pattern of Gq alpha/G11 alpha degradation was observed. Upon addition of the agonist, the rate of degradation initially increased markedly (t0.5 = 2.9 +/- 0.2 h). The maintained presence of the agonist was unable, however, to sustain the enhanced rate of degradation. Beyond 8 h of treatment with carbachol, degradation of Gq alpha/G11 alpha returned to a rate close to that observed in untreated cells (t0.5 = 18.5 +/- 1.3 h). Parallel experiments indicated that the effect of carbachol was specific for Gq alpha/G11 alpha, as the t0.5 of Gi2 alpha (approx. 30 h) was not affected by the agonist. Analysis of Gq alpha/G11 alpha mRNA levels by reverse transcriptase/PCR indicated that there was no difference in cells maintained in the absence and presence of carbachol. Such data demonstrate that agonist-induced establishment of a new steady-state level of Gq alpha/G11 alpha results from an initial receptor-mediated enhancement of protein turnover followed by a desensitization of the receptor response.
用胆碱能激动剂卡巴胆碱处理稳定表达人M1毒蕈碱型乙酰胆碱(HM1)受体的CHO细胞,会导致细胞中Gqα/G11α水平降低。3小时产生半数最大效应,随后建立约为Gqα/G11α静息水平50%的新稳态[Mullaney、Dodd、Buckley和Milligan,(1993年)《生物化学杂志》289卷,125 - 131页]。为分析此效应的机制,我们检测了在有和没有卡巴胆碱(1 mM)存在的情况下,这些表达HM1的细胞中Gqα/G11α的周转速率。在未处理的细胞中,35S标记的Gqα/G11α的实测去除情况可用半衰期(t0.5)为18.0±2.2小时的单指数曲线充分描述。当细胞用卡巴胆碱处理时,观察到Gqα/G11α降解的模式更为复杂。加入激动剂后,降解速率最初显著增加(t0.5 = 2.9±0.2小时)。然而,激动剂的持续存在无法维持增强的降解速率。在用卡巴胆碱处理超过8小时后,Gqα/G11α的降解速率恢复到接近未处理细胞中观察到的速率(t0.5 = 18.5±1.3小时)。平行实验表明,卡巴胆碱的效应对Gqα/G11α具有特异性,因为Gi2α的t0.5(约30小时)不受激动剂影响。通过逆转录酶/聚合酶链反应分析Gqα/G11α mRNA水平表明,在有和没有卡巴胆碱存在的情况下培养的细胞中没有差异。这些数据表明,激动剂诱导的Gqα/G11α新稳态水平的建立是由于最初受体介导的蛋白质周转增强,随后是受体反应的脱敏。