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肿瘤坏死因子α和一种神经酰胺酶抑制剂对人脂联素受体及其膜孕酮受体旁系同源物的拮抗作用。

Antagonism of human adiponectin receptors and their membrane progesterone receptor paralogs by TNFalpha and a ceramidase inhibitor.

作者信息

Kupchak Brian R, Garitaonandia Ibon, Villa Nancy Y, Smith Jessica L, Lyons Thomas J

机构信息

Department of Chemistry, University of Florida, P.O. Box 117200, Gainesville, Florida 32611, USA.

出版信息

Biochemistry. 2009 Jun 23;48(24):5504-6. doi: 10.1021/bi9006258.

Abstract

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.

摘要

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。

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