Jacquemin C, Thibout H, Lambert B, Correze C
Nature. 1986;323(6084):182-4. doi: 10.1038/323182a0.
Although cholera toxin induces a marked stimulation of adenylate cyclase activity in rat adipocyte plasma membranes, the holotoxin induces only a slight increase of cyclic AMP accumulation in intact cells. A similar apparent anomaly is seen with pertussis toxin, which has been shown to inhibit the Gi subunit of adenylate cyclase, and has a greater effect on cAMP accumulation and lipolysis than the activation by cholera toxin of the Gs subunit. To understand better the way in which these bacterial toxins are modifying the adipocyte cells, we prepared adipocyte plasma membranes and submitted them to ADP-ribosylation by cholera and pertussis toxins. During the incubation of control cells, we found endogenous ADP-ribosylation of Gs as a result of sustained stimulation of Gi by adenosine. Our results point to a possible homoeostatic system in which the autonomous adjustment of the basal activity of Gs as a function of that of Gi, under the control of feedback inhibitory ligands, ensures a steady production of cAMP within the cell.
尽管霍乱毒素能显著刺激大鼠脂肪细胞质膜中的腺苷酸环化酶活性,但全毒素在完整细胞中仅能引起环磷酸腺苷(cAMP)积累的轻微增加。百日咳毒素也存在类似的明显异常情况,该毒素已被证明可抑制腺苷酸环化酶的Gi亚基,并且与霍乱毒素激活Gs亚基相比,其对cAMP积累和脂解的影响更大。为了更好地理解这些细菌毒素修饰脂肪细胞的方式,我们制备了脂肪细胞质膜,并使其受到霍乱毒素和百日咳毒素的ADP核糖基化作用。在对照细胞的孵育过程中,我们发现由于腺苷对Gi的持续刺激,导致了Gs的内源性ADP核糖基化。我们的结果表明存在一种可能的稳态系统,在反馈抑制性配体的控制下,Gs的基础活性根据Gi的活性进行自主调节,从而确保细胞内cAMP的稳定产生。