Smoothened determines β-arrestin-mediated removal of the G protein-coupled receptor Gpr161 from the primary cilium

被引:99
|
作者
Pal, Kasturi [1 ]
Hwang, Sun-hee [1 ]
Somatilaka, Bandarigoda [1 ]
Badgandi, Hemant [1 ]
Jackson, Peter K. [2 ]
DeFea, Kathryn [3 ]
Mukhopadhyay, Saikat [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
[2] Stanford Univ, Sch Med, Dept Microbiol & Immunol, Stanford, CA 94305 USA
[3] Univ Calif Riverside, Div Biomed Sci, Riverside, CA 92521 USA
来源
JOURNAL OF CELL BIOLOGY | 2016年 / 212卷 / 07期
基金
美国国家卫生研究院;
关键词
ADRENERGIC-RECEPTOR; SONIC HEDGEHOG; SIGNAL-TRANSDUCTION; TRANSITION ZONE; KINASE; MEMBRANE; TRAFFICKING; COMPLEX; LOCALIZATION; PHOSPHORYLATION;
D O I
10.1083/jcb.201506132
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dynamic changes in membrane protein composition of the primary cilium are central to development and homeostasis, but we know little about mechanisms regulating membrane protein flux. Stimulation of the sonic hedgehog (Shh) pathway in vertebrates results in accumulation and activation of the effector Smoothened within cilia and concomitant disappearance of a negative regulator, the orphan G protein-coupled receptor (GPCR), Gpr161. Here, we describe a two-step process determining removal of Gprl 61 from cilia. The first step involves beta-arrestin recruitment by the signaling competent receptor, which is facilitated by the GPCR kinase Grk2. An essential factor here is the ciliary trafficking and activation of Smoothened, which by increasing Gpr161-beta-arrestin binding promotes Gpr161 removal, both during resting conditions and upon Shh pathway activation. The second step involves clathrin-mediated endocytosis, which functions outside of the ciliary compartment in coordinating Gprl 61 removal. Mechanisms determining dynamic compartmentalization of Gprl 61 in cilia define a new paradigm for down-regulation of GPCRs during developmental signaling from a specialized subcellular compartment.
引用
收藏
页码:861 / 875
页数:15
相关论文
共 50 条
  • [21] Arrestin recruitment and signaling by G protein-coupled receptor heteromers
    Mores, Kendall L.
    Cassell, Robert J.
    van Rijn, Richard M.
    NEUROPHARMACOLOGY, 2019, 152 : 15 - 21
  • [22] The Ciliary G-Protein-Coupled Receptor Gpr161 Negatively Regulates the Sonic Hedgehog Pathway via cAMP Signaling
    Mukhopadhyay, Saikat
    Wen, Xiaohui
    Ratti, Navneet
    Loktev, Alexander
    Rangell, Linda
    Scales, Suzie J.
    Jackson, Peter K.
    CELL, 2013, 152 (1-2) : 210 - 223
  • [23] Mechanism of β-arrestin recruitment by the μ-opioid G protein-coupled receptor
    Mafi, Amirhossein
    Kim, Soo-Kyung
    Goddard, William A., III
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2020, 117 (28) : 16346 - 16355
  • [24] Smoothened Signaling in Vertebrates Is Facilitated by a G Protein-coupled Receptor Kinase
    Philipp, Melanie
    Fralish, Gregory B.
    Meloni, Alison R.
    Chen, Wei
    MacInnes, Alyson W.
    Barak, Lawrence S.
    Caron, Marc G.
    MOLECULAR BIOLOGY OF THE CELL, 2008, 19 (12) : 5478 - 5489
  • [25] Competing G protein-coupled receptor kinases balance G protein and β-arrestin signaling
    Heitzler, Domitille
    Durand, Guillaume
    Gallay, Nathalie
    Rizk, Aurelien
    Ahn, Seungkirl
    Kim, Jihee
    Violin, Jonathan D.
    Dupuy, Laurence
    Gauthier, Christophe
    Piketty, Vincent
    Crepieux, Pascale
    Poupon, Anne
    Clement, Frederique
    Fages, Francois
    Lefkowitz, Robert J.
    Reiter, Eric
    MOLECULAR SYSTEMS BIOLOGY, 2012, 8
  • [26] GPR30: A G protein-coupled receptor for estrogen
    Prossnitz, Eric R.
    Arterburn, Jeffrey B.
    Sklar, Larry A.
    MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2007, 265 : 138 - 142
  • [27] Application of G Protein-Coupled Receptor-Heteromer Identification Technology to Monitor β-Arrestin Recruitment to G Protein-Coupled Receptor Heteromers
    See, Heng B.
    Seeber, Ruth M.
    Kocan, Martina
    Eidne, Karin A.
    Pfleger, Kevin D. G.
    ASSAY AND DRUG DEVELOPMENT TECHNOLOGIES, 2011, 9 (01) : 21 - 30
  • [28] The stability of the G protein-coupled receptor-β-arrestin interaction determines the mechanism and functional consequence of ERK activation
    Tohgo, A
    Choy, EW
    Gesty-Palmer, D
    Pierce, KL
    Laporte, S
    Oakley, RH
    Caron, MG
    Lefkowitz, RJ
    Luttrell, LM
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) : 6258 - 6267
  • [29] Cellular trafficking of G protein-coupled receptor/β-arrestin endocytic complexes
    Zhang, J
    Barak, LS
    Anborgh, PH
    Laporte, SA
    Caron, MG
    Ferguson, SSG
    JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) : 10999 - 11006
  • [30] The Diverse Roles of Arrestin Scaffolds in G Protein-Coupled Receptor Signaling
    Peterson, Yuri K.
    Luttrell, Louis M.
    PHARMACOLOGICAL REVIEWS, 2017, 69 (03) : 256 - 297