S100A12 in Digestive Diseases and Health: A Scoping Review

Author:

Carvalho Alexandre1,Lu Jacky2,Francis Jamisha D.2,Moore Rebecca E.3,Haley Kathryn P.4,Doster Ryan S.25,Townsend Steven D.3,Johnson Jeremiah G.6,Damo Steven M.789,Gaddy Jennifer A.2510ORCID

Affiliation:

1. Internal Medicine Program, St. Joseph Mercy Hospital, Ann Arbor, Michigan, USA

2. Department of Pathology, Microbiology, And Immunology, Vanderbilt University School of Medicine, Nashville, Tennessee, USA

3. Department of Chemistry, Vanderbilt University, Nashville, Tennessee, USA

4. Department of Biomedical Sciences, Grand Valley State University, Allendale, Michigan, USA

5. Division of Infectious Diseases, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA

6. Department of Microbiology, University of Tennessee, Knoxville, Tennessee, USA

7. Department of Life and Physical Sciences, Fisk University, Nashville, Tennessee, USA

8. Departments of Biochemistry and Chemistry, Vanderbilt University, Nashville, Tennessee, USA

9. Department of Structural Biology, Vanderbilt University, Nashville, Tennessee, USA

10. Tennessee Valley Healthcare Systems, Department of Veterans Affairs, Nashville, Tennessee, USA

Abstract

Calgranulin proteins are an important class of molecules involved in innate immunity. These members of the S100 class of the EF-hand family of calcium-binding proteins have numerous cellular and antimicrobial functions. One protein in particular, S100A12 (also called EN-RAGE or calgranulin C), is highly abundant in neutrophils during acute inflammation and has been implicated in immune regulation. Structure-function analyses reveal that S100A12 has the capacity to bind calcium, zinc, and copper, processes that contribute to nutritional immunity against invading microbial pathogens. S100A12 is a ligand for the receptor for advanced glycation end products (RAGE), toll-like receptor 4 (TLR4), and CD36, which promote cellular and immunological pathways to alter inflammation. We conducted a scoping review of the existing literature to define what is known about the association of S100A12 with digestive disease and health. Results suggest that S100A12 is implicated in gastroenteritis, necrotizing enterocolitis, gastritis, gastric cancer, Crohn’s disease, irritable bowel syndrome, inflammatory bowel disease, and digestive tract cancers. Together, these results reveal S100A12 is an important molecule broadly associated with the pathogenesis of digestive diseases.

Funder

National Center for Advancing Translational Sciences

Publisher

Hindawi Limited

Subject

Gastroenterology,Hepatology

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