Annexin-A1: Therapeutic Potential in Microvascular Disease

Front Immunol. 2019 Apr 30:10:938. doi: 10.3389/fimmu.2019.00938. eCollection 2019.

Abstract

Annexin-A1 (ANXA1) was first discovered in the early 1980's as a protein, which mediates (some of the) anti-inflammatory effects of glucocorticoids. Subsequently, the role of ANXA1 in inflammation has been extensively studied. The biology of ANXA1 is complex and it has many different roles in both health and disease. Its effects as a potent endogenous anti-inflammatory mediator are well-described in both acute and chronic inflammation and its role in activating the pro-resolution phase receptor, FPR2, has been described and is now being exploited for therapeutic benefit. In the present mini review, we will endeavor to give an overview of ANXA1 biology in relation to inflammation and functions that mediate pro-resolution that are independent of glucocorticoid induction. We will focus on the role of ANXA1 in diseases with a large inflammatory component focusing on diabetes and microvascular disease. Finally, we will explore the possibility of exploiting ANXA1 as a novel therapeutic target in diabetes and the treatment of microvascular disease.

Keywords: Annexin-A1 (ANXA1); diabetes; inflammation; signaling; tissue protection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Addison Disease / drug therapy
  • Addison Disease / immunology
  • Addison Disease / pathology
  • Animals
  • Annexin A1 / immunology*
  • Cushing Syndrome / drug therapy
  • Cushing Syndrome / immunology
  • Cushing Syndrome / pathology
  • Diabetes Mellitus / drug therapy
  • Diabetes Mellitus / immunology
  • Diabetes Mellitus / pathology
  • Glucocorticoids / immunology
  • Glucocorticoids / therapeutic use
  • Humans
  • Inflammation / drug therapy
  • Inflammation / immunology
  • Inflammation / pathology
  • Receptors, Formyl Peptide / immunology*
  • Receptors, Lipoxin / immunology*
  • Vascular Diseases / drug therapy
  • Vascular Diseases / immunology*
  • Vascular Diseases / pathology

Substances

  • ANXA1 protein, human
  • Annexin A1
  • FPR2 protein, human
  • Glucocorticoids
  • Receptors, Formyl Peptide
  • Receptors, Lipoxin