Kupchak Brian R, Garitaonandia Ibon, Villa Nancy Y, Smith Jessica L, Lyons Thomas J
Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, USA.
Biochemistry. 2009 Jun 23;48(24):5504-6. doi: 10.1021/bi9006258.
The progestin and AdipoQ receptor (PAQR) family of proteins comprises three distinct structural classes, each with seemingly different agonist specificities. For example, Class I receptors, like the human adiponectin receptors (AdipoR1 and AdipoR2), sense proteins with a particular three-dimensional fold, while Class II receptors are nonclassical membrane receptors for the steroid hormone progesterone. Using a previously developed heterologous expression system to study PAQR receptor activity, we demonstrate that human PAQRs from all three classes are antagonized by both 1(S),2(R)-d-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol, a ceramidase inhibitor, and TNFalpha, a homologue of adiponectin that functions antagonistically to both adiponectin and progesterone in human cells.
孕激素与脂联素受体(PAQR)蛋白家族包含三个不同的结构类别,每个类别似乎具有不同的激动剂特异性。例如,I类受体,如人类脂联素受体(AdipoR1和AdipoR2),感知具有特定三维折叠的蛋白质,而II类受体是类固醇激素孕酮的非经典膜受体。利用先前开发的异源表达系统研究PAQR受体活性,我们证明来自所有三个类别的人类PAQR均受到1(S),2(R)-d-赤藓糖-2-(N-肉豆蔻酰氨基)-1-苯基-1-丙醇(一种神经酰胺酶抑制剂)和TNFα(脂联素的同源物,在人类细胞中对脂联素和孕酮均起拮抗作用)的拮抗。