Constitutive agonist-independent CCR5 oligomerization and antibody-mediated clustering occurring at physiological levels of receptors

…, C Blanpain, M Parmentier, C Labbé-Jullié… - Journal of Biological …, 2002 - ASBMB
Although homo-oligomerization has been reported for several G protein-coupled receptors,
this phenomenon was not studied at low concentrations of receptors. Furthermore, it is not …

Biochemical and pharmacological activities of SR 142948A, a new potent neurotensin receptor antagonist

…, V Santucci, N Vita, F Pecceu, C Labbé-Jullié… - … of Pharmacology and …, 1997 - ASPET
SR 142948A, 2-{[5-(2,6-dimethoxyphenyl)-1-(4-(N-(3-dimethylaminopropyl)-N-methylcarbamoyl)-2-isopropylphenyl)-1H-pyrazole-3-carbonyl]amino}adamantane-2-carboxylic
acid, …

Cooperative regulation of extracellular signal-regulated kinase activation and cell shape change by filamin A and β-arrestins

…, A Thuret, O Muntaner, C Labbé-Jullié… - … and cellular biology, 2006 - Taylor & Francis
β-Arrestins (βarr) are multifunctional adaptor proteins that can act as scaffolds for G protein-coupled
receptor activation of mitogen-activated protein kinases (MAPK). Here, we identify …

An escort for GPCRs: implications for regulation of receptor density at the cell surface

L Achour, C Labbé-Jullié, MGH Scott… - Trends in pharmacological …, 2008 - cell.com
G-protein-coupled receptors (GPCRs) are dynamically regulated by various mechanisms
that tune their response to external stimuli. Modulation of their plasma membrane density, via …

Identification of the receptor subtype involved in the analgesic effect of neurotensin

I Dubuc, P Sarret, C Labbe-Jullie, JM Botto… - Journal of …, 1999 - Soc Neuroscience
The neuropeptide neurotensin (NT) elicits hypothermic and naloxone-insensitive analgesic
responses after brain injection. Recent pharmacological evidence obtained with NT agonists …

Homo-and hetero-oligomerization of β-arrestins in living cells

…, M Coppey-Moisan, M Bouvier, C Labbé-Jullié… - Journal of Biological …, 2005 - ASBMB
Arrestins are important proteins, which regulate the function of serpentine heptahelical receptors
and contribute to multiple signaling pathways downstream of receptors. The ubiquitous …

Agonism, inverse agonism, and neutral antagonism at the constitutively active human neurotensin receptor 2

F Richard, S Barroso, J Martinez, C Labbé-Jullié… - Molecular …, 2001 - ASPET
Two G protein-coupled neurotensin (NT) receptors, termed NTR1 and NTR2, have been
identified so far. In contrast to the NTR1, which has been extensively studied, little is known …

Identification of residues involved in neurotensin binding and modeling of the agonist binding site in neurotensin receptor 1

…, JM Bernassau, P Kitabgi, C Labbé-Jullié - Journal of Biological …, 2000 - ASBMB
The neurotensin receptor 1 (NTR1) subtype belongs to the family of G protein-coupled
receptors and mediates most of the known effects of the neuropeptide including modulation of …

Mutagenesis and modeling of the neurotensin receptor NTR1: Identification of residues that are critical for binding SR 48692, a nonpeptide neurotensin antagonist

C Labbé-Jullié, S Barroso, D Nicolas-Eteve… - Journal of Biological …, 1998 - ASBMB
The two neurotensin receptor subtypes known to date, NTR1 and NTR2, belong to the
family of G-protein-coupled receptors with seven putative transmembrane domains (TM). SR …

β-arrestin 2 oligomerization controls the Mdm2-dependent inhibition of p53

…, M Coppey-Moisan, C Labbé-Jullié… - Proceedings of the …, 2007 - National Acad Sciences
β-arrestins (β-arrs), two ubiquitous proteins involved in serpentine heptahelical receptor
regulation and signaling, form constitutive homo- and heterooligomers stabilized by inositol 1,2,3…