Metformin increases glucose uptake and acts renoprotectively by reducing SHIP2 activity. Issue 2 (15th October 2018)
- Record Type:
- Journal Article
- Title:
- Metformin increases glucose uptake and acts renoprotectively by reducing SHIP2 activity. Issue 2 (15th October 2018)
- Main Title:
- Metformin increases glucose uptake and acts renoprotectively by reducing SHIP2 activity
- Authors:
- Polianskyte-Prause, Zydrune
Tolvanen, Tuomas A.
Lindfors, Sonja
Dumont, Vincent
Van, Mervi
Wang, Hong
Dash, Surjya N.
Berg, Mika
Naams, Jette-Britt
Hautala, Laura C.
Nisen, Harry
Mirtti, Tuomas
Groop, Per-Henrik
Wähälä, Kristiina
Tienari, Jukka
Lehtonen, Sanna - Abstract:
- ABSTRACT: Metformin, the first‐line drug to treat type 2 diabetes (T2D), inhibits mitochondrial glycerolphosphate dehydrogenase in the liver to suppress gluconeogenesis. However, the direct target and the underlying mechanisms by which metformin increases glucose uptake in peripheral tissues remain uncharacterized. Lipid phosphatase Src homology 2 domain‐containing inositol‐5‐phosphatase 2 (SHIP2) is upregulated in diabetic rodent models and suppresses insulin signaling by reducing Akt activation, leading to insulin resistance and diminished glucose uptake. Here, we demonstrate that metformin directly binds to and reduces the catalytic activity of the recombinant SHIP2 phosphatase domain in vitro . Metformin inhibits SHIP2 in cultured cells and in skeletal muscle and kidney of db/db mice. In SHIP2‐overexpressing myotubes, metformin ameliorates reduced glucose uptake by slowing down glucose transporter 4 endocytosis. SHIP2 overexpression reduces Akt activity and enhances podocyte apoptosis, and both are restored to normal levels by metformin. SHIP2 activity is elevated in glomeruli of patients with T2D receiving nonmetformin medication, but not in patients receiving metformin, compared with people without diabetes. Furthermore, podocyte loss in kidneys of metformin‐treated T2D patients is reduced compared with patients receiving nonmetformin medication. Our data unravel a novel molecular mechanism by which metformin enhances glucose uptake and acts renoprotectively byABSTRACT: Metformin, the first‐line drug to treat type 2 diabetes (T2D), inhibits mitochondrial glycerolphosphate dehydrogenase in the liver to suppress gluconeogenesis. However, the direct target and the underlying mechanisms by which metformin increases glucose uptake in peripheral tissues remain uncharacterized. Lipid phosphatase Src homology 2 domain‐containing inositol‐5‐phosphatase 2 (SHIP2) is upregulated in diabetic rodent models and suppresses insulin signaling by reducing Akt activation, leading to insulin resistance and diminished glucose uptake. Here, we demonstrate that metformin directly binds to and reduces the catalytic activity of the recombinant SHIP2 phosphatase domain in vitro . Metformin inhibits SHIP2 in cultured cells and in skeletal muscle and kidney of db/db mice. In SHIP2‐overexpressing myotubes, metformin ameliorates reduced glucose uptake by slowing down glucose transporter 4 endocytosis. SHIP2 overexpression reduces Akt activity and enhances podocyte apoptosis, and both are restored to normal levels by metformin. SHIP2 activity is elevated in glomeruli of patients with T2D receiving nonmetformin medication, but not in patients receiving metformin, compared with people without diabetes. Furthermore, podocyte loss in kidneys of metformin‐treated T2D patients is reduced compared with patients receiving nonmetformin medication. Our data unravel a novel molecular mechanism by which metformin enhances glucose uptake and acts renoprotectively by reducing SHIP2 activity.—Polianskyte‐Prause, Z., Tolvanen, T. A., Lindfors, S., Dumont, V., Van, M., Wang, H., Dash, S. N., Berg, M., Naams, J.‐B., Hautala, L. C., Nisen, H., Mirtti, T., Groop, P.‐H., Wähälä, K., Tienari, J., Lehtonen, S. Metformin increases glucose uptake and acts renoprotectively by reducing SHIP2 activity. FASEB J. 33, 2858–2869 (2019). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 33:Issue 2(2019)
- Journal:
- FASEB journal
- Issue:
- Volume 33:Issue 2(2019)
- Issue Display:
- Volume 33, Issue 2 (2019)
- Year:
- 2019
- Volume:
- 33
- Issue:
- 2
- Issue Sort Value:
- 2019-0033-0002-0000
- Page Start:
- 2858
- Page End:
- 2869
- Publication Date:
- 2018-10-15
- Subjects:
- diabetic kidney disease -- insulin resistance -- lipid phosphatase -- podocyte -- type 2 diabetes
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201800529RR ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13220.xml