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National Institute of Environmental Health Sciences

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Publication Detail

Title: Targeted Proteomic Analysis of Small GTPases in Murine Adipogenesis.

Authors: Yang, Yen-Yu; Huang, Ming; Wang, Yinsheng

Published In Anal Chem, (2020 May 05)

Abstract: Small GTPases are essential signaling molecules for regulating glucose uptake in adipose tissues upon insulin stimulation, and this regulation maintains an appropriate range of glycemia. The involvement of small GTPases in adipogenesis, however, has not been systemically investigated. In this study, we applied a high-throughput scheduled multiple-reaction monitoring (MRM) method, along with the use of synthetic stable isotope-labeled peptides, to identify differentially expressed small GTPase proteins during adipogenesis of cultured murine cells. We were able to quantify the relative levels of expression of 55 and 49 small GTPases accompanied by adipogenic differentiation in 3T3-L1 and C3H10T1/2 cells, respectively. When compared with analysis conducted in the data-dependent acquisition (DDA) mode, the MRM-based proteomic platform substantially increased the coverage of the small GTPase proteome. Western blot analysis further corroborated the MRM quantification results for selected small GTPases. Interestingly, overall a significant number of small GTPases were down-regulated during adipogenesis. Among them, the expression levels of Rab32 protein were consistently lower in differentiated adipocytes than the corresponding undifferentiated precursors in both cell lines. Overexpression of Rab32 in 3T3-L1 and C3H10T1/2 cells prior to adipogenesis induction suppressed their differentiation. Together, this is the first comprehensive analysis of the alterations in small GTPase proteome during adipogenesis, and we reveal a previously unrecognized role of Rab32 in adipogenic differentiation.

PubMed ID: 32237738 Exiting the NIEHS site

MeSH Terms: 3T3-L1 Cells; Adipocytes/metabolism; Adipogenesis; Animals; Cell Differentiation; Cells, Cultured; Chromatography, Liquid; GTP Phosphohydrolases/analysis*; GTP Phosphohydrolases/metabolism; High-Throughput Screening Assays; Mice; Proteomics*; Tandem Mass Spectrometry

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