Weng G, Feinstein D, Reis D, Wahlestedt C
Department of Neurology and Neuroscience, Cornell University Medical College, New York, NY 10021, USA.
Regul Pept. 1996 May 7;63(1):53-6. doi: 10.1016/0167-0115(96)00030-4.
The mouse adrenocortical Y-1 cell line expresses a high level of neuropeptide Y1 receptor (NPY-Y1). Moreover the receptor density can be up-regulated by dexamethasone or down-regulated by cAMP. To determine whether such regulation occurs at the level of gene expression, Y1 receptor mRNA was measured using a reverse transcriptase-competitive PCR method. Dexamethasone treatment increased Y1 mRNA in Y-1 cells, whereas the cAMP and ACTH decreased it. We also observed that the amount of Y1 receptor RNA was unaffected by phorbol 12-myristate 13-acetate, a protein kinase C stimulator, but was abolished in a cell line expressing apolipoprotein E (apoE). The results indicated that NPY-Y1 receptor mRNA in Y-1 cells is highly regulated by several intracellular messengers. The role of apoE in such regulation is of particular interest in view of evidence that the isoform of the molecule is highly correlated to the age of onset of Alzheimer's disease. The effect observed in the Y-1 cell line which expresses apoE may implicate a possible role of this protein in the process of neuronal death that occurred in the Alzheimer's disease.
小鼠肾上腺皮质Y-1细胞系表达高水平的神经肽Y1受体(NPY-Y1)。此外,受体密度可被地塞米松上调或被cAMP下调。为了确定这种调节是否发生在基因表达水平,使用逆转录竞争性PCR方法测量Y1受体mRNA。地塞米松处理增加了Y-1细胞中的Y1 mRNA,而cAMP和促肾上腺皮质激素则使其减少。我们还观察到,Y1受体RNA的量不受蛋白激酶C刺激剂佛波酯12-肉豆蔻酸酯13-乙酸酯的影响,但在表达载脂蛋白E(apoE)的细胞系中被消除。结果表明,Y-1细胞中的NPY-Y1受体mRNA受到多种细胞内信使的高度调节。鉴于有证据表明该分子的异构体与阿尔茨海默病的发病年龄高度相关,apoE在这种调节中的作用尤其令人感兴趣。在表达apoE的Y-1细胞系中观察到的效应可能暗示了这种蛋白质在阿尔茨海默病中发生的神经元死亡过程中的可能作用。