Wang S Z, Hu J R, Long R M, Pou W S, Forray C, el-Fakahany E E
Department of Pharmacology and Toxicology, University of Maryland School of Pharmacy, Baltimore 21201.
FEBS Lett. 1990 Dec 10;276(1-2):185-8. doi: 10.1016/0014-5793(90)80538-t.
Agonist-induced reduction in both the number of m1 muscarinic receptors and the mRNA coding for the receptor protein was investigated in Chinese hamster ovary (CHO) cells which were transfected with the m1 muscarinic receptor gene. Receptor concentration was measured by the specific binding of the muscarinic ligand, [3H]quinuclidinyl benzilate ([3H]QNB), and Northern blot hybridization analysis was used to evaluate the levels of receptor mRNA. Incubation of cells with 1 mM of the muscarinic agonist, carbamylcholine (CBC), for 24 h decreased receptor density and mRNA levels in cells by 65% and 73%, respectively. These results indicate that agonist-induced down-regulation of m1 muscarinic receptors might be due to, at least in part, a decrease in receptor synthesis resulting from a reduction in the steady-state level of their mRNA.
在中国仓鼠卵巢(CHO)细胞中,研究了激动剂诱导的m1毒蕈碱受体数量和编码该受体蛋白的mRNA的减少情况,这些细胞已转染了m1毒蕈碱受体基因。通过毒蕈碱配体[3H]喹核醇基苯甲酸酯([3H]QNB)的特异性结合来测量受体浓度,并使用Northern印迹杂交分析来评估受体mRNA的水平。用1 mM毒蕈碱激动剂氨甲酰胆碱(CBC)孵育细胞24小时,可使细胞中的受体密度和mRNA水平分别降低65%和73%。这些结果表明,激动剂诱导的m1毒蕈碱受体下调可能至少部分是由于其mRNA稳态水平降低导致受体合成减少所致。