PTPR£f Protein expression could be the link between obesity and insulin resistance in liver cells found a new study
Highlights
- By deciphering PTPR£f protein, the factors linking obesity and insulin resistance and role played by the liver in the onset of type 2 diabetes has been discovered
- The expansion of fat cells, a characteristic of obesity, leads to an increase in inflammatory signals
- PTPR£f content in liver may increase upon inflammation and this could directly affect insulin receptors by inhibiting insulin action leading to diabetes
The expansion of fat cells, a characteristic of obesity, leads to an increase in inflammatory signals that have effects on the liver as well as on several other organs.
Obesity-induced inflammation triggers the activation of a transcription factor called NF-k£], which seems to be instrumental in the development of diabetes. But what are the exact cellular and molecular mechanisms at stake and how could they lead to new therapeutic strategies?
"To answer these questions, we focused on a protein called PTPR£f (for Protein Tyrosine Phosphatase Receptor Gamma), which is a target of NF-k£]", explains Professor Roberto Coppari, coordinator of the UNIGE Faculty of Medicine Diabetes Centre.
"We first examined various human cohorts: these human studies indicated that PTPR£f content in liver increases upon inflammation, an effect that could directly affect insulin receptors by inhibiting insulin action", he adds.
To test their hypothesis, the scientists modified the levels of PTPR£f expression in mice, by either suppressing, normally expressing or over expressing it, and observed the effect on insulin resistance.
"The mice totally lacking PTPR£f, when put on a high-calorie diet, did develop obesity. But they did not show any sign of insulin resistance and seemed to be entirely protected from diet-induced diabetes", explains Xavier Brenachot, a researcher at UNIGE Faculty of Medicine and first author of this study.
To fine-tune their analysis, Roberto Coppari and his colleagues reconstituted the expression of PTPR£f at normal levels, but only in hepatocytes (liver cells). The mice were again prone to insulin resistance, indicating the pivotal role of the liver.
Moreover, a two-fold over expression in the liver (mimicking the natural patho-physiology of obesity) was sufficient to cause insulin resistance.
Can this PTPR£f protein be used as therapeutic target?
The metabolic functions of this protein were never characterized; this discovery therefore opens the door for potential new therapies. Previous studies had already studied PTP proteins in search for diabetes treatments, unfortunately to no avail.
However, contrary to some of its family members that are intra-cellular, the protein identified in Geneva is located on the cell membrane. It is therefore of much easier access for therapeutic molecules.
Interestingly, the very form of this protein allows for potential inhibition strategies: when two independent PTPR£f molecules are brought together by a ligand, they cannot act any more. The researchers are now working on identifying the endogenous ligand produced by the body, or on developing molecules that could mimic its function.
"This study would not have been possible without the UNIGE Faculty Diabetes Center, established in 2015 to enhance interactions between clinical and basic researchers", indicates Roberto Coppari.
"Indeed, our research started with clinical observations made by Prof. Francesco Negro - also a member of UNIGE Faculty Diabetes Center - at the University Hospitals of Geneva. We now hope that our preclinical and clinical results will in turn be translated into clinical progress and contribute to a better management of type-2 diabetes that, today, affects 1 in 11 adults globally, or 422 million people."
Reference
- Xavier Brenachot, Giorgio Ramadori, Rafael M. Ioris, Christelle Veyrat-Durebex, Jordi Altirriba, Ebru Aras, Sanda Ljubicic, Daisuke Kohno, Salvatore Fabbiano, Sophie Clement, Nicolas Goossens, Mirko Trajkovski, Sheila Harroch, Francesco Negro & Roberto Coppari. Hepatic protein tyrosine phosphatase receptor gamma links obesity-induced inflammation to insulin resistance, Nature Communications (2017) . DOI:10.1038/s41467-017-02074-2
Source-Eurekalert