Drummond I A, Chisholm R L
Department of Cell Biology and Anatomy, Northwestern University Medical School, Chicago, IL 60611.
Dev Genet. 1988;9(4-5):293-301. doi: 10.1002/dvg.1020090411.
We have analyzed the effects of the cAMP relay inhibitor, caffeine, and the receptor antagonist, adenosine, on the regulation of the cell-surface cAMP receptor in suspension-starved Dictyostelium discoideum cells by measuring ammonium sulfate-stabilized binding of [3-H]cAMP to intact cells. When cells were starved in fast (230 r.p.m.) shaken suspension in 10 mM Na+/5 mM K+ phosphate buffer, pH 6.5, plus 1 mM CaCl2 and 2.5 mM MgCl2, and assayed for specific cAMP binding, receptor accumulation peaked at approximately 6 hours, reaching a maximum of 1.5 pmol cAMP bound/10(7) cells (saturation binding). Neither caffeine nor adenosine inhibited the accumulation of cAMP receptors. Similar results were obtained in caffeine-treated, slow shaken (90 r.p.m.) suspension cultures. These results suggest that starvation alone is sufficient stimulus to induce the cAMP receptor. We have also tested the effects of different buffer ionic compositions on the accumulation of cAMP receptors. Elevation of the monovalent ion concentration to 30-40 mM was found to significantly inhibit the induction of cAMP receptors.
我们通过测量硫酸铵稳定的[3-H]cAMP与完整细胞的结合,分析了cAMP信号转导抑制剂咖啡因和受体拮抗剂腺苷对悬浮饥饿的盘基网柄菌细胞表面cAMP受体调节的影响。当细胞在10 mM Na+/5 mM K+磷酸盐缓冲液(pH 6.5)、1 mM CaCl2和2.5 mM MgCl2中,于快速(230转/分钟)振荡悬浮液中饥饿,并测定特异性cAMP结合时,受体积累在约6小时达到峰值,最高达到1.5 pmol cAMP结合/10(7)个细胞(饱和结合)。咖啡因和腺苷均未抑制cAMP受体的积累。在咖啡因处理的、缓慢振荡(90转/分钟)的悬浮培养物中也得到了类似结果。这些结果表明,仅饥饿就足以刺激诱导cAMP受体。我们还测试了不同缓冲液离子组成对cAMP受体积累的影响。发现单价离子浓度升高至30-40 mM会显著抑制cAMP受体的诱导。