Literature DB >> 19249352

G protein-coupled receptors stimulation and the control of cell migration.

Mathieu Cotton1, Audrey Claing.   

Abstract

Cell migration is a fundamental biological process involved in normal physiology. Altered motile phenotypes are however often associated with the development and progression of diseases such as cancer and atherosclerosis. Remodeling of the actin cytoskeleton is required for cell shape changes and is controlled by a broad variety of cellular proteins. Interestingly, several extracellular stimuli can promote actin reorganization and result in enhanced cell migration. Namely, G protein-coupled receptors (GPCRs), which are activated by factors ranging from small amines, to hormones, and chemokines, initiate signalling cascades resulting in cell shape changes, formation of a migrating front (leading edge) and altered adhesion. GPCRs are heptahelical membrane proteins, which classically transmit signal via the activation of heterotrimeric G proteins. Sustained stimulation leads to the activation of G protein-coupled receptor kinases (GRKs) and the recruitment of arrestin proteins, which engage alternative signalling pathways. In this review, we will discuss the role of GPCR mediated signal transduction and review their importance in the regulation of actin remodeling leading to cell migration.

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Year:  2009        PMID: 19249352     DOI: 10.1016/j.cellsig.2009.02.008

Source DB:  PubMed          Journal:  Cell Signal        ISSN: 0898-6568            Impact factor:   4.315


  76 in total

Review 1.  BAR domain competition during directional cellular migration.

Authors:  Gabriel A Quiñones; Anthony E Oro
Journal:  Cell Cycle       Date:  2010-07-01       Impact factor: 4.534

2.  The orphan adhesion G protein-coupled receptor GPR97 regulates migration of lymphatic endothelial cells via the small GTPases RhoA and Cdc42.

Authors:  Nadejda Valtcheva; Adriana Primorac; Giorgia Jurisic; Maija Hollmén; Michael Detmar
Journal:  J Biol Chem       Date:  2013-10-31       Impact factor: 5.157

3.  RanBPM protein acts as a negative regulator of BLT2 receptor to attenuate BLT2-mediated cell motility.

Authors:  Jun-Dong Wei; Joo-Young Kim; Ae-Kyoung Kim; Sung Key Jang; Jae-Hong Kim
Journal:  J Biol Chem       Date:  2013-08-08       Impact factor: 5.157

Review 4.  Astrocytes in Migration.

Authors:  Jiang Shan Zhan; Kai Gao; Rui Chao Chai; Xi Hua Jia; Dao Peng Luo; Guo Ge; Yu Wu Jiang; Yin-Wan Wendy Fung; Lina Li; Albert Cheung Hoi Yu
Journal:  Neurochem Res       Date:  2016-11-11       Impact factor: 3.996

5.  The Ric-8A/Gα13/FAK signalling cascade controls focal adhesion formation during neural crest cell migration in Xenopus.

Authors:  Gabriela Toro-Tapia; Soraya Villaseca; Andrea Beyer; Alice Roycroft; Sylvain Marcellini; Roberto Mayor; Marcela Torrejón
Journal:  Development       Date:  2018-11-21       Impact factor: 6.868

6.  Genetic Deletion of β-Arrestin-2 and the Mitigation of Established Airway Hyperresponsiveness in a Murine Asthma Model.

Authors:  Minyong Chen; Akhil Hegde; Yeon Ho Choi; Barbara S Theriot; Richard T Premont; Wei Chen; Julia K L Walker
Journal:  Am J Respir Cell Mol Biol       Date:  2015-09       Impact factor: 6.914

7.  The small GTPase Arf6 regulates sea urchin morphogenesis.

Authors:  Nadezda A Stepicheva; Megan Dumas; Priscilla Kobi; Julie G Donaldson; Jia L Song
Journal:  Differentiation       Date:  2017-02-02       Impact factor: 3.880

Review 8.  Non-traditional roles of G protein-coupled receptors in basic cell biology.

Authors:  Xin Zhang; Ulrike S Eggert
Journal:  Mol Biosyst       Date:  2013-04-05

9.  The interplay between G protein-coupled receptor kinase 2 (GRK2) and histone deacetylase 6 (HDAC6) at the crossroads of epithelial cell motility.

Authors:  Vanesa Lafarga; Federico Mayor; Petronila Penela
Journal:  Cell Adh Migr       Date:  2012-10-17       Impact factor: 3.405

10.  G(i)-coupled GPCR signaling controls the formation and organization of human pluripotent colonies.

Authors:  Kenta Nakamura; Nathan Salomonis; Kiichiro Tomoda; Shinya Yamanaka; Bruce R Conklin
Journal:  PLoS One       Date:  2009-11-10       Impact factor: 3.240

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