Functional analysis of the Ala67Thr polymorphism in agouti related protein associated with anorexia nervosa and leanness

被引:15
作者
de Rijke, CE
Jackson, PJ
Garner, KM
van Rozen, RJ
Douglas, NR
Kas, MJH
Millhauser, GL
Adan, RAH
机构
[1] Univ Utrecht, Med Ctr, Dept Pharmacol & Anat, Rudolf Magnus Inst Neurosci, NL-3584 CG Utrecht, Netherlands
[2] Univ Calif Santa Cruz, Dept Chem & Biochem, Santa Cruz, CA 95064 USA
关键词
agouti related protein; melanocortin receptors; polymorphism; recombinant expression; weight regulation; anorexia;
D O I
10.1016/j.bcp.2005.04.033
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
AgRP is a neuropeptide that stimulates food intake through inhibition of central melanocortin receptors (MCRs), In humans, the non-conservative amino acid substitution Alanine (Ala) 67 Threonine (Thr) has been associated with Anorexia Nervosa and with leanness. In the present study, the cellular distribution, processing and in vitro and in vivo activities of Ala67 and Thr67 AgRP were investigated. Western blots of media and lysates of BHK cells stably transfected with Ala67 or Thr67 expression constructs showed identical AgRP bands. Both Ala67 and Thr67 AgRP colocalised with the Golgi apparatus, but not with the ER or lysmsomes when expressed in Att20 D16V cells. Also, no differences were observed between the potencies of bacterially expressed Ala67 and Thr67 AgRP to stimulate MC4R in a reporter gene assay or inhibit food intake in rats. Taken together, no evidence was found fora functional defect of Thr67 AgRP related to MC4R interactions. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:308 / 316
页数:9
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