Neuraminidase-induced externalization of phosphatidylserine activates ADAM17 and impairs insulin signaling in endothelial cells

Author:

Ferreira-Santos Larissa1ORCID,Ramirez-Perez Francisco I.1ORCID,Foote Christopher A.12,Augenreich Marc A.13ORCID,McMillan Neil J.13ORCID,Williams Morgan B.1ORCID,Gonzalez-Vallejo Juan D.1ORCID,Power Gavin13,Wheeler Andrew A.4ORCID,Manrique-Acevedo Camila156ORCID,Martinez-Lemus Luis A.127ORCID,Padilla Jaume136ORCID

Affiliation:

1. NextGen Precision Health, University of Missouri, Columbia, Missouri, United States

2. Department of Medical Pharmacology and Physiology, University of Missouri, Columbia, Missouri, United States

3. Department of Nutrition and Exercise Physiology, University of Missouri, Columbia, Missouri, United States

4. Department of Surgery, University of Missouri, Columbia, Missouri, United States

5. Division of Endocrinology and Metabolism, Department of Medicine, University of Missouri, Columbia, Missouri, United States

6. Harry S. Truman Memorial Veterans’ Hospital, Columbia, Missouri, United States

7. Center for Precision Medicine, Department of Medicine, University of Missouri, Columbia, Missouri, United States

Abstract

This work provides the first evidence that neuraminidase, an enzyme increased in the circulation of men and women with type 2 diabetes (T2D), promotes anoctamin-6 (ANO6)-dependent externalization of phosphatidylserine in endothelial cells, which in turn leads to activation of a disintegrin and metalloproteinase-17 (ADAM17) and consequent shedding of the insulin receptor-α from the cell surface. Hence, this work supports that consideration should be given to the neuraminidase-ANO6-ADAM17 axis as a novel potential target for restoring endothelial insulin sensitivity in T2D.

Funder

HHS | NIH | National Heart, Lung, and Blood Institute

HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases

Research Excellence Program at the University of Missouri-Columbia

Life Sciences Fellowship at the University of Missouri-Columbia

HHS | NIH | National Institute of General Medical Sciences

American Heart Association

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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