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Identification and characterization of adipose surface epitopes.

Biochem. J. 477, 2509-2541 (2020)
Publ. Version/Full Text DOI PMC
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Adipose tissue is a central regulator of metabolism and an important pharmacological target to treat the metabolic consequences of obesity, such as insulin resistance and dyslipidemia. Among the various cellular compartments, the adipocyte cell surface is especially appealing as a drug target as it contains various proteins that when activated or inhibited promote adipocyte health, change its endocrine function and eventually maintain or restore whole-body insulin sensitivity. In addition, cell surface proteins are readily accessible by various drug classes. However, targeting individual cell surface proteins in adipocytes has been difficult due to important functions of these proteins outside adipose tissue, raising various safety concerns. Thus, one of the biggest challenges is the lack of adipose selective surface proteins and/or targeting reagents. Here, we discuss several receptor families with an important function in adipogenesis and mature adipocytes to highlight the complexity at the cell surface and illustrate the problems with identifying adipose selective proteins. We then discuss that, while no unique adipocyte surface protein might exist, how splicing, posttranslational modifications as well as protein/protein interactions can create enormous diversity at the cell surface that vastly expands the space of potentially unique epitopes and how these selective epitopes can be identified and targeted.
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Publication type Article: Journal article
Document type Review
Corresponding Author
Keywords Adipogenesis ; Brown Adipose Tissue ; Insulin Resistance ; Obesity ; Surface Markers ; White Adipose Tissue
ISSN (print) / ISBN 0264-6021
e-ISSN 1470-8728
Quellenangaben Volume: 477, Issue: 13, Pages: 2509-2541 Article Number: , Supplement: ,
Publisher Portland Press
Non-patent literature Publications
Reviewing status Peer reviewed