4.6 Article

The Increased Expression of Regulator of G-Protein Signaling 2 (RGS2) Inhibits Insulin-Induced Akt Phosphorylation and Is Associated with Uncontrolled Glycemia in Patients with Type 2 Diabetes

期刊

METABOLITES
卷 11, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/metabo11020091

关键词

Akt protein; HbA1c; human endothelial cells; insulin resistance; palmitic acid; regulator of G-protein signaling 2; type 2 diabetes mellitus

资金

  1. Center for Research and Advanced Studies of the National Polytechnic Institute
  2. CONACYT/SEP Research Grant [167673]
  3. Estimulo a la Investigacion Medica Miguel Aleman Valdes 2018
  4. CONACYT [FC2016/2803]
  5. Autonomous University of Baja California

向作者/读者索取更多资源

Experimental evidence in mice models has shown that high levels of the regulator of G-protein signaling 2 (RSG2) protein are associated with insulin resistance, and in patients with type 2 diabetes mellitus, platelet RGS2 expression levels were higher than in healthy donors. Overexpression of RGS2 in human endothelial cells leads to decreased insulin signaling and is linked to poorly controlled diabetes.
Experimental evidence in mice models has demonstrated that a high regulator of G-protein signaling 2 (RSG2) protein levels precede an insulin resistance state. In the same context, a diet rich in saturated fatty acids induces an increase in RGS2 protein expression, which has been associated with decreased basal metabolism in mice; however, the above has not yet been analyzed in humans. For this reason, in the present study, we examined the association between RGS2 expression and insulin resistance state. The incubation with palmitic acid (PA), which inhibits insulin-mediated Akt Ser(473) phosphorylation, resulted in the increased RGS2 expression in human umbilical vein endothelial-CS (HUVEC-CS) cells. The RGS2 overexpression without PA was enough to inhibit insulin-mediated Akt Ser(473) phosphorylation in HUVEC-CS cells. Remarkably, the platelet RGS2 expression levels were higher in type 2 diabetes mellitus (T2DM) patients than in healthy donors. Moreover, an unbiased principal component analysis (PCA) revealed that RGS2 expression level positively correlated with glycated hemoglobin (HbA1c) and negatively with age and high-density lipoprotein cholesterol (HDL) in T2DM patients. Furthermore, PCA showed that healthy subjects segregated from T2DM patients by having lower levels of HbA1c and RGS2. These results demonstrate that RGS2 overexpression leads to decreased insulin signaling in a human endothelial cell line and is associated with poorly controlled diabetes.

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