Does Metformin Modulate Endoplasmic Reticulum Stress and Autophagy in Type 2 Diabetic Peripheral Blood Mononuclear Cells?


Por: Diaz-Morales N, Iannantuoni F, Escribano-Lopez I, Bañuls C, Rovira-Llopis S, Sola E, Rocha M, Hernandez-Mijares A and Victor VM

Publicada: 1 jun 2018 Ahead of Print: 1 nov 2017
Resumen:
Since type 2 diabetes (T2D) is associated with oxidative stress and metformin has been shown to exert a protective role against the said stress, we wondered whether metformin treatment might also modulate endoplasmic reticulum (ER) stress and autophagy in leukocytes of T2D patients. We studied 53 T2D patients (37 of whom had been treated with metformin 1700mg for at least 1 year) and 30 healthy volunteers. Leukocytes from both groups of T2D patients exhibited increased protein levels of 78-kDa glucose-regulated protein (GRP78) with respect to controls, whereas activating transcription factor 6 (ATF6) was enhanced specifically in nonmetformin-treated T2D, and s-xbp1 and phosphorylated eukaryotic initiation factor 2 (p-eIF2) increased only in the metformin-treated group. The autophagy markers becn1, atg7, and microtubule-associated protein 1A/1B-light chain 3II/I (LC3 II/I) increased in nonmetformin-treated T2D, and metformin treatment reduced mitochondrial superoxide and increased glutathione (GSH) levels. Our observations raise the question of whether metformin treatment could reduce oxidative stress and act as an ER stress modulator in T2D patients by promoting an adaptive unfolded protein response (s-xbp1 and p-eIF2) in their leukocytes; this was in contrast with nonmetformin-treated patients whose response could be driven by the ATF6-dependent pro-apoptotic pathway. Further, our findings lead to us to form the hypothesis of an autophagy-dependent clearance of misfolded proteins in nonmetformin-treated T2D patients that could be repressed by metformin treatment.Antioxid. Redox Signal. 00, 000-000.

Filiaciones:
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 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

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 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

 2 CIBERehd-Department of Pharmacology and Physiology, University of Valencia , Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

 3 Institute of Health Research INCLIVA, University of Valencia , Valencia, Spain

 4 Department of Medicine, University of Valencia , Valencia, Spain

:
 1 Service of Endocrinology, University Hospital Doctor Peset , Foundation for the Promotion of Health and Biomedical Research in the Valencian Region (FISABIO), Valencia, Spain

 2 CIBERehd-Department of Pharmacology and Physiology, University of Valencia , Valencia, Spain

 5 Department of Physiology, University of Valencia , Valencia, Spain
ISSN: 15230864





ANTIOXIDANTS & REDOX SIGNALING
Editorial
MARY ANN LIEBERT, INC, United States, Estados Unidos America
Tipo de documento: News Item
Volumen: 28 Número: 17
Páginas: 1562-1569
WOS Id: 000417254500001
ID de PubMed: 29061071

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