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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 15: Adhesion GPCRs as Modulators of Immune Cell Function.
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Chapter title
Adhesion GPCRs as Modulators of Immune Cell Function.
Chapter number 15
Book title
Adhesion G Protein-coupled Receptors
Published in
Handbook of experimental pharmacology, November 2016
DOI 10.1007/978-3-319-41523-9_15
Pubmed ID
Book ISBNs
978-3-31-941521-5, 978-3-31-941523-9
Authors

Jörg Hamann, Cheng-Chih Hsiao, Chang Sup Lee, Kodi S. Ravichandran, Hsi-Hsien Lin

Editors

Tobias Langenhan, Torsten Schöneberg

Abstract

Immune cells express several adhesion G protein-coupled receptors (aGPCRs), including the ADGRE subfamily members EMR1 (F4/80, ADGRE1), EMR2 (ADGRE2), EMR3 (ADGRE3), EMR4 (FIRE, ADGRE4), and CD97 (ADGRE5), the ADGRB subfamily member BAI1 (ADGRB1), and the ADGRG subfamily members GPR56 (ADGRG1), GPR97 (Pb99, ADGRG3), and GPR114 (ADGRG5). Expression of these molecules in hematopoietic stem and progenitor cells, monocytes/macrophages (Mφs), dendritic cells, granulocytes, and lymphocytes depends on lineage diversification and maturation, making them suitable markers for individual leukocyte subsets (e.g., F4/80 on mouse Mφs). Recent studies revealed intriguing activities of aGPCRs in tolerance induction (EMR1), granulopoiesis (CD97), engulfment of apoptotic cells and bacteria (BAI1), hematopoietic stem cell formation (GPR56), and control of cytotoxicity (GPR56). Here, we review these findings and discuss their biological and translational implications.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 32 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 32 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 22%
Researcher 6 19%
Student > Bachelor 4 13%
Professor 2 6%
Student > Master 2 6%
Other 1 3%
Unknown 10 31%
Readers by discipline Count As %
Immunology and Microbiology 6 19%
Biochemistry, Genetics and Molecular Biology 5 16%
Agricultural and Biological Sciences 4 13%
Medicine and Dentistry 2 6%
Veterinary Science and Veterinary Medicine 1 3%
Other 3 9%
Unknown 11 34%