Adiponectin's globular domain inhibits T cell activation by interacting with LAIR-1

Biochem Biophys Res Commun. 2021 Oct 8:573:117-124. doi: 10.1016/j.bbrc.2021.08.025. Epub 2021 Aug 12.

Abstract

Adiponectin (APN) is the most abundant adipokine in human plasma, and has insulin-sensitizing effect. Recent studies have reported that APN plays both anti- and pro-inflammatory roles under different circumstances. However, there is a lack of convincing evidence that decipher APN's anti-inflammatory role through the known receptors and their downstream signaling pathways. In this study, we evaluated a new molecular mechanism underlying APN's anti-inflammatory roles. Our results revealed that the globular domain of adiponectin (gAdp) interacted with the inhibitory leukocyte-associated immunoglobulin-like receptor-1 (LAIR-1). In vitro experiments showed that gAdp inhibited activation of the T cells via the LAIR-1, through a process that also involved downstream SHP-2. These findings indicate that LAIR-1 is a novel APN receptor, affirming APN's anti-inflammatory effect. In summary, we have identified a novel mechanism of peripheral immunoregulatory processes that provides baseline information for further studies on gAdp's role and its contribution to inflammation.

Keywords: Adiponectin; LAIR-1; SHP-2; T cell activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adiponectin / pharmacology*
  • Anti-Inflammatory Agents / pharmacology*
  • HEK293 Cells
  • Humans
  • Ligands
  • Receptors, Immunologic / antagonists & inhibitors*
  • Receptors, Immunologic / immunology
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / immunology

Substances

  • Adiponectin
  • Anti-Inflammatory Agents
  • Ligands
  • Receptors, Immunologic
  • leukocyte-associated immunoglobulin-like receptor 1