Single-transmembrane domain IGF-II/M6P receptor:Potential interaction with g protein and its association with cholesterol-rich membrane domains

Amritraj, Asha and Posse De Chaves, Elena I. and Hawkes, Cheryl and MacDonald, Richard G. and Kar, Satyabrata (2012) Single-transmembrane domain IGF-II/M6P receptor:Potential interaction with g protein and its association with cholesterol-rich membrane domains. Endocrinology, 153 (10). pp. 4784-4798. ISSN 0013-7227

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Abstract

The IGF-II/mannose 6-phosphate (M6P) receptor is a single-transmembrane domain glycoprotein that plays an important role in the intracellular trafficking of lysosomal enzymes and endocytosis-mediated degradation of IGF-II. The receptor may also mediate certain biological effects in response to IGF-II binding by interacting with G proteins. However, the nature of the IGF-II/M6P receptor's interaction with the G protein or with G protein-coupled receptor (GPCR) interacting proteins such as β-arrestin remains unclear. Here we report that [125I]IGF-II receptor binding in the rat hippocampal formation is sensitive to guanosine-5′-[γ-thio]triphosphate, mastoparan, and Mas-7, which are known to interfere with the coupling of the classical GPCR with G protein. Monovalent and divalent cations also influenced [125I]IGF-II receptor binding. The IGF-II/M6P receptor, as observed for several GPCRs, was found to be associated with β-arrestin 2, which exhibits sustained ubiquitination after stimulation with Leu27IGF-II, an IGF-II analog that binds rather selectively to the IGF-II/M6P receptor. Activation of the receptor by Leu27IGF-II induced stimulation of extracellular signal-related kinase 1/2 via a pertussis toxin-dependent pathway. Additionally, we have shown that IGF-II/M6P receptors under normal conditions are associated mostly with detergent- resistant membrane domains, but after stimulation with Leu27IGF-II, are translocated to the detergent-soluble fraction along with a portion of β-arrestin 2. Collectively these results suggest that the IGF-II/M6P receptor may interact either directly or indirectly with G protein as well as β-arrestin 2, and activation of the receptor by an agonist can lead to alteration in its subcellular distribution along with stimulation of an intracellular signaling cascade.

Item Type:
Journal Article
Journal or Publication Title:
Endocrinology
Uncontrolled Keywords:
/dk/atira/pure/subjectarea/asjc/1300/1310
Subjects:
ID Code:
137309
Deposited By:
Deposited On:
07 Oct 2019 08:35
Refereed?:
Yes
Published?:
Published
Last Modified:
01 Jan 2020 12:16