Characterisation of the adiponectin receptors: The non-conserved N-terminal region of AdipoR2 prevents its expression at the cell-surface

被引:10
作者
Keshvari, Sahar [1 ]
Rose, Felicity J. [1 ]
Charlton, Hayley K. [1 ]
Scheiber, Nicole L. [2 ,3 ]
Webster, Julie [1 ]
Kim, Yu-Hee [1 ]
Choaping Ng [1 ]
Parton, Robert G. [2 ]
Whitehead, Jonathan P. [1 ]
机构
[1] Mater Med Res Inst, Brisbane, Qld, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, Brisbane, Qld, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Adipokine; Seven-transmembrane receptor; AdipoR; PAQR; Cell-surface expression; PROTEINS; PATHWAY; BINDING;
D O I
10.1016/j.bbrc.2013.01.092
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adiponectin is a beneficial adipokine with insulin-sensitizing, anti-inflammatory and anti-atherogenic effects. These effects are mediated by two poorly characterised, closely related, atypical seven-transmembrane receptors. In the current report we have used C-terminal, epitope-tagged AdipoR1 and AdipoR2 constructs to monitor cell-surface expression by indirect immunofluorescence microscopy and quantitative plate-based analysis. We demonstrate that only AdipoR1 is constitutively expressed on the cell-surface. Further investigations, involving characterisation of a number of chimeric and truncated constructs, show the non-conserved region of AdipoR2 (residues 1-81) restricts its cell-surface expression;Introduction or deletion of this region, into AdipoR1 or AdipoR2, resulted in inhibition or promotion of cell-surface expression, respectively. We also confirmed that AdipoR1 and AdipoR2 can form heterodimers when co-expressed and that co-expression leads to the cell-surface expression of AdipoR2. Collectively these studies demonstrate that the non-conserved region of AdipoR2 restricts its cell-surface expression and raise the possibility that the majority of cell-surface AdipoR2 may be present in the form of heterodimers. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:28 / 33
页数:6
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