Muscle-specific inflammation induced by MCP-1 overexpression does not affect whole-body insulin sensitivity in mice

• Published in: Diabetologia 2016-03, Vol.59 (3), p.624-633
• Main Authors: Evers-van Gogh, Inkie J. A., Oteng, Antwi-Boasiako, Alex, Sheril, Hamers, Nicole, Catoire, Milene, Stienstra, Rinke, Kalkhoven, Eric, Kersten, Sander
• Format: Article
• Language: English
• Subjects: Animals; Body fat; Chemokine CCL2 - genetics; Chemokine CCL2 - metabolism; Chemokines; Cytokines; Diabetes; Diabetes Mellitus, Type 2 - metabolism; Glucose; Human Physiology; Hypotheses; Inflammation; Inflammation - metabolism; Insulin resistance; Insulin Resistance - genetics; Insulin Resistance - physiology; Internal Medicine; Male; MCP-1; Medicine; Medicine & Public Health; Metabolic Diseases; Metabolism; Mice; Muscle, Skeletal - metabolism; Muscle-specific; Musculoskeletal system; Myokine; Nutrition; Obesity; Plasma; Proteins; Type 2 diabetes
• ISSN: 0012-186X; 1432-0428
• DOI: 10.1007/s00125-015-3822-2

Aims/hypothesis Obesity is associated with a state of chronic low-grade inflammation that is believed to contribute to the development of skeletal muscle insulin resistance. However, the extent to which local and systemic elevation of cytokines, such as monocyte chemoattractant protein 1 (MCP-1), interferes with the action of insulin and promotes insulin resistance and glucose intolerance in muscle remains unclear. Here, we aim to investigate the effect of muscle-specific overexpression of MCP-1 on insulin sensitivity and glucose tolerance in lean and obese mice. Methods We used Mck – Mcp-1 transgenic (Tg) mice characterised by muscle-specific overexpression of Mcp-1 (also known as Ccl2 ) and elevated plasma MCP-1 levels. Mice were fed either chow or high-fat diet for 10 weeks. Numerous metabolic variables were measured, including glucose and insulin tolerance tests, muscle insulin signalling and plasma NEFA, triacylglycerol, cholesterol, glucose and insulin. Results Despite clearly promoting skeletal muscle inflammation, muscle-specific overexpression of Mcp- 1 did not influence glucose tolerance or insulin sensitivity in either lean chow-fed or diet-induced obese mice. In addition, plasma NEFA, triacylglycerol, cholesterol, glucose and insulin were not affected by MCP-1 overexpression. Finally, in vivo insulin-induced Akt phosphorylation in skeletal muscle did not differ between Mcp-1 -Tg and wild-type mice. Conclusions/interpretation We show that increased MCP-1 production in skeletal muscle and concomitant elevated MCP-1 levels in plasma promote inflammation in skeletal muscle but do not influence insulin signalling and have no effect on insulin resistance and glucose tolerance in lean and obese mice. Overall, our data argue against MCP-1 promoting insulin resistance in skeletal muscle and raise questions about the impact of inflammation on insulin sensitivity in muscle.