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Adhesion G Protein-coupled Receptors

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Cover of 'Adhesion G Protein-coupled Receptors'

Table of Contents

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    Book Overview
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    Chapter 1 Introduction: History of the Adhesion GPCR Field.
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    Chapter 2 Classification, Nomenclature, and Structural Aspects of Adhesion GPCRs.
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    Chapter 3 7TM Domain Structure of Adhesion GPCRs.
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    Chapter 4 Understanding the Structural Basis of Adhesion GPCR Functions.
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    Chapter 5 Control of Adhesion GPCR Function Through Proteolytic Processing.
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    Chapter 6 Tethered Agonism: A Common Activation Mechanism of Adhesion GPCRs.
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    Chapter 7 Versatile Signaling Activity of Adhesion GPCRs.
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    Chapter 8 Adhesion G Protein-coupled Receptors
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    Chapter 9 The Relevance of Genomic Signatures at Adhesion GPCR Loci in Humans.
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    Chapter 10 Adhesion GPCRs as a Putative Class of Metabotropic Mechanosensors.
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    Chapter 11 Adhesion GPCRs Govern Polarity of Epithelia and Cell Migration.
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    Chapter 12 Adhesion GPCRs as Novel Actors in Neural and Glial Cell Functions: From Synaptogenesis to Myelination.
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    Chapter 13 Control of Skeletal Muscle Cell Growth and Size Through Adhesion GPCRs.
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    Chapter 14 Adhesion GPCR Function in Pulmonary Development and Disease.
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    Chapter 15 Adhesion GPCRs as Modulators of Immune Cell Function.
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    Chapter 16 Heart Development, Angiogenesis, and Blood-Brain Barrier Function Is Modulated by Adhesion GPCRs.
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    Chapter 17 Adhesion GPCRs in Tumorigenesis.
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    Chapter 18 Erratum to: 7TM Domain Structure of Adhesion GPCRs
Attention for Chapter 13: Control of Skeletal Muscle Cell Growth and Size Through Adhesion GPCRs.
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Chapter title
Control of Skeletal Muscle Cell Growth and Size Through Adhesion GPCRs.
Chapter number 13
Book title
Adhesion G Protein-coupled Receptors
Published in
Handbook of experimental pharmacology, November 2016
DOI 10.1007/978-3-319-41523-9_13
Pubmed ID
Book ISBNs
978-3-31-941521-5, 978-3-31-941523-9
Authors

James P. White, White, James P.

Editors

Tobias Langenhan, Torsten Schöneberg

Abstract

Skeletal muscle homeostasis is regulated by a constant influx of chemicals and exposure to mechanical stimuli. A number of key signaling pathways that translate these stimuli into changes in muscle physiology have been established. The GPCR family known as adhesion GPCRs (aGPCRs) has largely elusive roles in skeletal muscle biology; however, their unique capacity to activate adhesion and G protein signaling pathways makes them an attractive point of investigation. The skeletal muscle myofiber contains a highly organized cytoarchitecture to ensure contractile function. This requires intricate interactions with components of the extracellular matrix (ECM) surrounding each fiber. aGPCRs possess extended N-termini known to interact with ECM proteins and complexes suggesting a compatible role in skeletal muscle biology. Furthermore, recent work demonstrated the involvement of certain aGPCRs in whole muscle hypertrophy and differentiation of muscle progenitor cells. Signaling pathways downstream of aGPCRs are still incompletely understood; however, initial findings show involvement of the Gα12/13 subunit signaling to the pro-anabolic Akt/mTOR pathway. Together, this chapter will review the emerging role of aGPCRs in skeletal muscle biology and putative mechanism(s) employed to regulate skeletal muscle growth.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 12 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 12 100%

Demographic breakdown

Readers by professional status Count As %
Other 2 17%
Student > Master 2 17%
Student > Ph. D. Student 2 17%
Student > Postgraduate 2 17%
Researcher 1 8%
Other 1 8%
Unknown 2 17%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 25%
Medicine and Dentistry 2 17%
Pharmacology, Toxicology and Pharmaceutical Science 1 8%
Neuroscience 1 8%
Engineering 1 8%
Other 0 0%
Unknown 4 33%