Remodeling our concept of chemokine receptor function: From monomers to oligomers.

J Leukoc Biol

Department of Immunology and Oncology, Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.

Published: August 2018

AI Article Synopsis

  • Chemokines are crucial in directing the movement of leukocytes during both normal and inflammatory immune responses by binding to G protein-coupled receptors.
  • Advances in research over the past 25 years have revealed important details about how chemokines interact with receptors and their roles in various immune processes.
  • Recent biophysical techniques have demonstrated that chemokine receptors can form complex structures, such as dimers and oligomers, highlighting the intricate networks in which they operate and suggesting new potential therapeutic targets.

Article Abstract

The chemokines direct leukocyte recruitment in both homeostatic and inflammatory conditions, and are therefore critical for immune reactions. By binding to members of the class A G protein-coupled receptors, the chemokines play an essential role in numerous physiological and pathological processes. In the last quarter century, the field has accumulated much information regarding the implications of these molecules in different immune processes, as well as mechanistic insight into the signaling events activated through their binding to their receptors. Here, we will focus on chemokine receptors and how new methodological approaches have underscored the role of their conformations in chemokine functions. Advances in biophysical-based techniques show that chemokines and their receptors act in very complex networks and therefore should not be considered isolated entities. In this regard, the chemokine receptors can form homo- and heterodimers as well as oligomers at the cell surface. These findings are changing our view as to how chemokines influence cell biology, identify partners that regulate chemokine function, and open new avenues for therapeutic intervention.

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Source
http://dx.doi.org/10.1002/JLB.2MR1217-503RDOI Listing

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