Plakoglobin regulates adipocyte differentiation independently of the Wnt/ β-catenin signaling pathway

The scaffold protein 14-3-3 zeta is an established regulator of adipogenesis and postnatal adiposity. We and others have demonstrated the 14-3-3 zeta interactome to be diverse and dynamic, and it can be examined to identify novel regulators of physiological processes, including adipogenesis. In the present study, we sought to determine if factors that influence adipogenesis during the development of obesity could be identified in the 14-3-3 zeta interactome found in white adipose tissue of lean or obese TAP-tagged-14-3-3 zeta overexpressing mice. Using mass spectrometry, differences in the abundance of novel, as well as established, adipogenic factors within the 14-3-3 zeta interactome could be detected in adipose tissues. One novel candidate was revealed to be plakoglobin, the homolog of the known adipogenic inhibitor, beta-catenin, and herein, we report that plakoglobin is involved in adipocyte differentiation. Plakoglobin is expressed in murine 3T3 -L1 cells and is primarily localized to the nucleus, where its abundance decreases during adipogenesis. Depletion of plakoglobin by siRNA inhibited adipogenesis and reduced PPAR gamma 2 expression, and similarly, plakoglobin depletion in human adipose-derived stem cells also impaired adipogenesis and reduced lipid accumulation post-differentiation. Transcriptional assays indicated that plakoglobin does not participate in Wnt/beta-catenin signaling, as its depletion did not affect Wnt3amediated transcriptional activity. Taken together, our results establish plakoglobin as a novel regulator of adipogenesis in vitro and highlights the ability of using the 14-3-3 zeta interactome to identify potential pro-obesogenic factors.