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Journal of Obesity
Volume 2013 (2013), Article ID 476240, 7 pages
Research Article

PTPIP51: A New Interaction Partner of the Insulin Receptor and PKA in Adipose Tissue

1Institute of Anatomy and Cell Biology, Justus Liebig University Giessen, Aulweg 123, 35392 Giessen, Germany
2Department of Neurology, Justus Liebig University Giessen, 35392 Giessen, Germany
3Department of Sports Medicine, Justus Liebig University Giessen, 35394 Giessen, Germany

Received 5 November 2012; Accepted 8 February 2013

Academic Editor: Francesco Saverio Papadia

Copyright © 2013 M. A. Bobrich et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.


Aims. Our previous experiments revealed an association of PTPIP51 (protein tyrosine phosphatase interacting protein 51) with the insulin signalling pathway through PTP1B and 14-3-3beta. We aimed to clarify the role of PTPIP51 in adipocyte metabolism. Methods. Four groups of ten C57Bl/6 mice each were used. Two groups were fed a standard diet; two groups were fed a high-fat diet. Two groups (one high-fat diet and one standard diet) were submitted to endurance training, while the remaining two groups served as untrained control groups. After ten weeks, we measured glucose tolerance of the mice. Adipose tissue samples were analyzed by immunofluorescence and Duolink proximity ligation assay to quantify interactions of PTPIP51 with either insulin receptor (IR) or PKA. Results. PTPIP51 and the IR and PTPIP51 and PKA, respectively, were colocalized in all groups. Standard diet animals that were submitted to endurance training showed low PTPIP51-IR and PTPIP51-PKA interactions. The interaction levels of both the IR and PKA differed between the feeding and training groups. Conclusion. PTPIP51 might serve as a linking protein in adipocyte metabolism by connecting the IR-triggered lipogenesis with the PKA-dependent lipolysis. PTPIP51 interacts with both proteins, therefore being a potential gateway for the cooperation of both pathways.