Olansky L, Myers G A, Pohl S L, Hewlett E L
Proc Natl Acad Sci U S A. 1983 Nov;80(21):6547-51. doi: 10.1073/pnas.80.21.6547.
Pertussis toxin (PT), a protein produced by Bordetella pertussis, was studied for its effect on lipolysis in isolated rat epididymal adipocytes. Exposure of adipocytes to pertussis toxin resulted in a significant increase in cyclic AMP levels and lipolysis after a lag of 1-2 hr. Both the maximal rate of lipolysis and the time lag (beyond 1 hr) were PT concentration-dependent. Heat treatment (95 degrees C, 30 min) or incubation with specific antibody directed against PT eliminated the ability of toxin to increase lipolysis. Cell-free culture medium from B. pertussis, but not from nontoxigenic Bordetella species, had the same effect on lipolysis as purified toxin. Comparison of the PT effect with the known lipolytic effect of cholera toxin (CT) revealed that the two toxins elicited responses that were indistinguishable in time course and magnitude. In contrast, the adenylate cyclase (EC 4.6.1.1) activities in membranes prepared from PT- or CT-treated adipocytes were different. Adenylate cyclase activity in membranes from control (untreated) adipocytes was inhibited 35-64% by the adenosine analogue N6-(L-2-phenylisopropyl)-adenosine. As expected from previous studies, membranes from CT-treated adipocytes demonstrated an increased basal activity but showed the same proportional inhibition by N6-(L-2-phenylisopropyl)-adenosine as controls. On the other hand, membranes from adipocytes exposed to PT (400 ng/ml for 4 hr) showed no increase in basal adenylate cyclase activity but had reduced sensitivity to N6-(L-2-phenylisopropyl)-adenosine inhibition, with the maximal effect ranging from 11 to 30% at 10(-6) M N6-(L-2-phenylisopropyl)-adenosine. These data support the hypothesis that PT promotes cyclic AMP-dependent lipolysis in a manner quantitatively equivalent to CT, but by a different mechanism involving increased cyclic AMP levels resulting from loss of responsiveness to endogenous inhibitors such as adenosine.
百日咳毒素(PT)是百日咳博德特氏菌产生的一种蛋白质,研究了其对分离的大鼠附睾脂肪细胞中脂肪分解的影响。脂肪细胞暴露于百日咳毒素后,经过1-2小时的延迟,环磷酸腺苷(cAMP)水平和脂肪分解显著增加。脂肪分解的最大速率和时间延迟(超过1小时)均与PT浓度相关。热处理(95℃,30分钟)或与针对PT的特异性抗体孵育可消除毒素增加脂肪分解的能力。来自百日咳博德特氏菌的无细胞培养基,但不是来自无毒博德特氏菌属的培养基,对脂肪分解的作用与纯化毒素相同。将PT的作用与已知的霍乱毒素(CT)的脂解作用进行比较,发现这两种毒素引发的反应在时间进程和幅度上无法区分。相反,由PT或CT处理的脂肪细胞制备的膜中的腺苷酸环化酶(EC 4.6.1.1)活性不同。腺苷类似物N6-(L-2-苯异丙基)-腺苷可抑制对照(未处理)脂肪细胞膜中的腺苷酸环化酶活性35-64%。正如先前研究所预期的那样,CT处理的脂肪细胞膜显示基础活性增加,但对N6-(L-2-苯异丙基)-腺苷的抑制比例与对照相同。另一方面,暴露于PT(400 ng/ml,4小时)的脂肪细胞膜的基础腺苷酸环化酶活性没有增加,但对N6-(L-2-苯异丙基)-腺苷抑制的敏感性降低,在10^(-6) M N6-(L-2-苯异丙基)-腺苷时最大抑制作用为11%至30%。这些数据支持以下假设:PT以与CT在数量上等效的方式促进cAMP依赖性脂肪分解,但通过不同的机制,即由于对内源性抑制剂如腺苷的反应性丧失导致cAMP水平升高。