Paris H, Bouscarel B, Cortinovis C, Murat J C
FEBS Lett. 1985 May 6;184(1):82-6. doi: 10.1016/0014-5793(85)80658-x.
The human colon adenocarcinoma cell-line HT 29 has been shown to possess functional alpha 2-adrenergic receptors. Here, [3H] clonidine was used as radioligand to study the evolution of alpha 2-adrenergic receptivity during the time course of HT 29 cell culture. Scatchard analysis of the saturation curves indicates that the number of [3H]clonidine binding sites increases throughout the 17 day culture period. The maximal number of alpha 2-adrenoceptors is found during the stationary phase of growth, when cell density is high and mitotic rate low. Moreover, the use of adrenaline and clonidine as alpha 2-adrenergic agonists reveals a relationship between the number of receptors and the intensity of the biological effect associated with their stimulation (inhibition of the VIP-induced cyclic AMP accumulation).
人结肠腺癌细胞系HT 29已被证明具有功能性α2 - 肾上腺素能受体。在此,[3H]可乐定用作放射性配体,以研究HT 29细胞培养过程中α2 - 肾上腺素能受体敏感性的演变。对饱和曲线的Scatchard分析表明,在整个17天的培养期内,[3H]可乐定结合位点的数量增加。当细胞密度高且有丝分裂率低时,在生长的静止期发现α2 - 肾上腺素能受体的最大数量。此外,使用肾上腺素和可乐定作为α2 - 肾上腺素能激动剂揭示了受体数量与其刺激相关的生物学效应强度(抑制VIP诱导的环磷酸腺苷积累)之间的关系。