Protection Against Insulin Resistance by Apolipoprotein M/Sphingosine-1-Phosphate

Author:

Kurano Makoto1ORCID,Tsukamoto Kazuhisa23,Shimizu Tomo4,Kassai Hidetoshi5,Nakao Kazuki5,Aiba Atsu5,Hara Masumi6,Yatomi Yutaka1ORCID

Affiliation:

1. Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

2. Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan

3. Department of Metabolism, Diabetes and Nephrology, Aizu Medical Center, Fukushima Medical University, Fukushima, Japan

4. Research & Development Division, Tsukuba Research Institute, Sekisui Medical Co., Ltd., Ibaraki, Japan

5. Laboratory of Animal Resources, Center for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

6. Department of Internal Medicine, Mizonokuchi Hospital, Teikyo University School of Medicine, Kanagawa, Japan

Abstract

Subjects with low serum HDL cholesterol levels are reported to be susceptible to diabetes, with insulin resistance believed to be the underlying pathological mechanism. Apolipoprotein M (apoM) is a carrier of sphingosine-1-phosphate (S1P), a multifunctional lipid mediator, on HDL, and the pleiotropic effects of HDL are believed to be mediated by S1P. In the current study, we attempted to investigate the potential association between apoM/S1P and insulin resistance. We observed that the serum levels of apoM were lower in patients with type 2 diabetes and that they were negatively correlated with BMI and the insulin resistance index. While deletion of apoM in mice was associated with worsening of insulin resistance, overexpression of apoM was associated with improvement of insulin resistance. Presumably, apoM/S1P exerts its protective effect against insulin resistance by activating insulin signaling pathways, such as the AKT and AMPK pathways, and also by improving the mitochondrial functions through upregulation of SIRT1 protein levels. These actions of apoM/S1P appear to be mediated via activation of S1P1 and/or S1P3. These results suggest that apoM/S1P exerts protective roles against the development of insulin resistance.

Funder

Japan Society for the Promotion of Science

Mitsukoshi Health and Welfare Foundation 2017

Japan Heart Foundation

MSD Life Science Foundation, Public Interest Incorporated Foundation

Japan Agency for Medical Research and Development

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

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