Major pharmacological distinction of the ACTH receptor from other melanocortin receptors

被引:145
作者
Schioth, HB
Chhajlani, V
Muceniece, R
Klusa, V
Wikberg, JES
机构
[1] UPPSALA UNIV,DEPT PHARMACEUT PHARMACOL,UPPSALA,SWEDEN
[2] LATVIAN ACAD SCI,INST ORGAN SYNTH,PHARMACOL LAB,LV-226006 RIGA,LATVIA
[3] WA PHARM,UMEA,SWEDEN
关键词
melanocortin receptor subtypes; I-125] [Nle(4); D-Phe(7)]alpha-MSH ligand binding; ACTH; Y1;
D O I
10.1016/0024-3205(96)00370-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The mouse adrenocortical cell line Y1, that expresses ACTH receptors (MC2R), was used to probe the binding of ACTH and MSH peptides by using radio-labelled ACTH (1-39). The Y1 cells were found to bind [I-125]-labelled ACTH(1-39) with high affinity (K-d similar to 130 pM). However, none of the melanocortin peptides NDP-MSH, alpha-MSH, beta-MSH or gamma 1-MSH could compete with the binding of the labelled ACTH(1-39). When other MC receptor subtype DNAs (MC1, MC3 and MC4) were transfected into the Y1 cells, characteristic binding of the [I-125]NDP-MSH appeared for each of the receptor subtype, but no specific binding was present in non-transfected cells. This is the first report clearly demonstrating that the ACTH receptor binds only ACTH, but not other melanocortin peptides.
引用
收藏
页码:797 / 801
页数:5
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