TIMP3 Overexpression in Macrophages Protects From Insulin Resistance, Adipose Inflammation, and Nonalcoholic Fatty Liver Disease in Mice
- Rossella Menghini1,
- Viviana Casagrande1,
- Stefano Menini2,
- Arianna Marino1,
- Valeria Marzano1,3,
- Marta L. Hribal4,
- Paolo Gentileschi5,
- Davide Lauro1,
- Orazio Schillaci6,7,
- Giuseppe Pugliese2,
- Paolo Sbraccia1,
- Andrea Urbani1,3,
- Renato Lauro1 and
- Massimo Federici1⇓
- 1Department of Internal Medicine, University of Rome “Tor Vergata,” Rome, Italy
- 2Department of Clinical and Molecular Medicine, “Sapienza” University, Rome, Italy
- 3Laboratory of Proteomics, EBRI/Santa Lucia Foundation, Rome, Italy
- 4Department of Medical and Surgical Sciences, University of Magna Graecia, Catanzaro, Italy
- 5Department of Surgery, University of Rome “Tor Vergata,” Rome, Italy
- 6Department of Diagnostic Imaging, University of Rome “Tor Vergata,” Rome, Italy
- 7Istituto di Ricovero e Cura a Carattere Scientifico Neuromed, Pozzilli, Italy
- Corresponding author: Massimo Federici, .
R.M. and V.C. contributed equally to this study.
The tissue inhibitor of metalloproteinase (TIMP)3, a stromal protein that restrains the activity of proteases and receptors, is reduced in inflammatory metabolic disorders such as type 2 diabetes mellitus (T2DM) and atherosclerosis. We overexpressed Timp3 in mouse macrophages (MacT3) to analyze its potential antidiabetic and antiatherosclerotic effects. Transgenic mice with myeloid cells targeting overexpression of TIMP3 were generated and fed a high-fat diet for 20 weeks. Physical and metabolic phenotypes were determined. Inflammatory markers, lipid accumulation, and insulin sensitivity were measured in white adipose tissue (WAT), liver, and skeletal muscle. In a model of insulin resistance, MacT3 mice were more glucose tolerant and insulin sensitive than wild-type mice in both in vitro and in vivo tests. Molecular and biochemical analyses revealed that increased expression of TIMP3 restrained metabolic inflammation and stress-related pathways, including Jun NH2-terminal kinase and p38 kinase activation, in WAT and liver. TIMP3 overexpression in macrophages resulted in reduced activation of oxidative stress signals related to lipid peroxidation, protein carbonylation, and nitration in WAT and liver. Our data show that macrophage-specific overexpression of TIMP3 protects from metabolic inflammation and related metabolic disorders such as insulin resistance, glucose intolerance, and nonalcoholic steatohepatitis.
This article contains Supplementary Data online at http://diabetes.diabetesjournals.org/lookup/suppl/doi:10.2337/db11-0613/-/DC1.
- Received May 9, 2011.
- Accepted November 21, 2011.
- © 2012 by the American Diabetes Association.
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