Diabetes 51:1859-1866, 2002
© 2002 by the American Diabetes Association, Inc.
Tanis: A Link Between Type 2 Diabetes and Inflammation?
Ken Walder1,
Lakshmi Kantham1,
Janine S. McMillan1,
James Trevaskis1,
Lyndal Kerr1,
Andrea de Silva1,
Terry Sunderland1,
Nathan Godde1,
Yuan Gao1,
Natalie Bishara1,
Kelly Windmill1,
Janette Tenne-Brown1,
Guy Augert2,
Paul Z. Zimmet3, and
Greg R. Collier1,4
1 Metabolic Research Unit, School of Health Sciences, Deakin University, Waurn Ponds, Victoria, Australia
2 Lipha SA Research and Development, Lyon, France
3 International Diabetes Institute, Caulfield, Australia
4 Autogen, South Melbourne, Australia
Here we describe a novel protein, which we have named Tanis, that is implicated in type 2 diabetes and inflammation. In Psammomys obesus, a unique polygenic animal model of type 2 diabetes and the metabolic syndrome, Tanis is expressed in the liver in inverse proportion to circulating glucose (P = 0.010) and insulin levels (P = 0.004) and in direct proportion with plasma triglyceride concentrations (P = 0.007). Hepatic Tanis gene expression was markedly increased (3.1-fold) after a 24-h fast in diabetic but not in nondiabetic P. obesus. In addition, glucose inhibited Tanis gene expression in cultured hepatocytes (P = 0.006) as well as in several other cell types (P = 0.0010.011). Thus, Tanis seems to be regulated by glucose and is dysregulated in the diabetic state. Yeast-2 hybrid screening identified serum amyloid A (SAA), an acute-phase inflammatory response protein, as an interacting protein of Tanis, and this was confirmed by Biacore experiments. SAA and other acute-phase proteins have been the focus of recent attention as risk factors for cardiovascular disease, and we contend that Tanis and its interaction with SAA may provide a mechanistic link among type 2 diabetes, inflammation, and cardiovascular disease.

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Copyright © 2002 by the American Diabetes Association.
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