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Annexin-A1: Therapeutic Potential in Microvascular Disease.
- Source :
-
Frontiers in immunology [Front Immunol] 2019 Apr 30; Vol. 10, pp. 938. Date of Electronic Publication: 2019 Apr 30 (Print Publication: 2019). - Publication Year :
- 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.
- Subjects :
- Addison Disease drug therapy
Addison Disease immunology
Addison Disease pathology
Animals
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
Vascular Diseases drug therapy
Vascular Diseases pathology
Annexin A1 immunology
Receptors, Formyl Peptide immunology
Receptors, Lipoxin immunology
Vascular Diseases immunology
Subjects
Details
- Language :
- English
- ISSN :
- 1664-3224
- Volume :
- 10
- Database :
- MEDLINE
- Journal :
- Frontiers in immunology
- Publication Type :
- Academic Journal
- Accession number :
- 31114582
- Full Text :
- https://doi.org/10.3389/fimmu.2019.00938