The Many and Varied Roles of Tetraspanins in Immune Cell Recruitment and Migration
Immune cell recruitment and migration is central to the normal functioning of the immune system in health and disease. Numerous adhesion molecules on immune cells and the parenchymal cells they interact with are well recognized for their roles in facilitating the movements of immune cells throughout...
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Published in | Frontiers in immunology Vol. 9; p. 1644 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
18.07.2018
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Subjects | |
Online Access | Get full text |
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Summary: | Immune cell recruitment and migration is central to the normal functioning of the immune system in health and disease. Numerous adhesion molecules on immune cells and the parenchymal cells they interact with are well recognized for their roles in facilitating the movements of immune cells throughout the body. A growing body of evidence now indicates that tetraspanins, proteins known for their capacity to organize partner molecules within the cell membrane, also have significant impacts on the ability of immune cells to migrate around the body. In this review, we examine the tetraspanins expressed by immune cells and endothelial cells that influence leukocyte recruitment and motility and describe their impacts on the function of adhesion molecules and other partner molecules that modulate the movements of leukocytes. In particular, we examine the functional roles of CD9, CD37, CD63, CD81, CD82, and CD151. This reveals the diversity of the functions of the tetraspanin family in this setting, both in the nature of adhesive and migratory interactions that they regulate, and the positive or inhibitory effects mediated by the individual tetraspanin proteins. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-3 content type line 23 ObjectType-Review-1 Edited by: Carlos Cabañas, Consejo Superior de Investigaciones Científicas (CSIC), Spain Reviewed by: Francisco Sanchez-Madrid, Universidad Autonoma de Madrid, Spain; Martin Johannes Hoogduijn, Erasmus University Rotterdam, Netherlands; Eric Rubinstein, INSERM U935 Modèles de Cellules Souches Malignes et Thérapeutiques, France Specialty section: This article was submitted to Antigen Presenting Cell Biology, a section of the journal Frontiers in Immunology |
ISSN: | 1664-3224 1664-3224 |
DOI: | 10.3389/fimmu.2018.01644 |