Abstract
Inter-organ communication is central to mammalian metabolism, allowing for the coordination of crucial homeostatic processes such as food intake, body weight, and blood glucose. Dissecting this process at a cellular and molecular level requires the establishment of a reductionist system in which cell types of interest can be investigated as the source and target of biologically relevant signals. Here, we describe a system to study the interaction between adipocytes and hepatocytes using either conditioned media from cultured adipocytes or co-culture of hepatocytes with adipose explants. These methods have the potential to identify novel polypeptides and metabolites involved in the adipose-liver metabolic axis.
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References
Rosen ED, Spiegelman BM (2014) What we talk about when we talk about fat. Cell 156:20–44
Zhang Y, Proenca R, Maffei M et al (1994) Positional cloning of the mouse obese gene and its human homologue. Nature 372:425–432
Cook KS, Min HY, Johnson D et al (1987) Adipsin: a circulating serine protease homolog secreted by adipose tissue and sciatic nerve. Science 237:402–405
Scherer PE, Williams S, Fogliano M et al (1995) A novel serum protein similar to C1q, produced exclusivelt in adipocytes. J Biol Chem 270:26746–26749
Steppan CM, Bailey ST, Bhat S et al (2001) The hormone resistin links obesity to diabetes. Nature 409:307–312
Yang Q, Graham TE, Mody N et al (2005) Serum retinol binding protein 4 contributes to insulin resistance in obesity and type 2 diabetes. Nature 436:356–362
Dahlman I, Elsen M, Tennagels N et al (2012) Functional annotation of the human fat cell secretome. Arch Physiol Biochem 118:84–91
Roca-Rivada A, Belen Bravo S, Perez-Sotelo D et al (2015) CILAIR-based secretome analysis of obese visceral and subcutaneous adipose tissue reveals distinctive ECM remodeling and inflammation mediators. Sci Rep. doi:10.1038/srep12214
Cohen P, Levy JD, Zhang Y et al (2014) Ablation of PRDM16 and beige adipose causes metabolic dysfunction and a subcutaneous to visceral fat switch. Cell 156:304–316
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O’Connor, S., Cohen, P. (2017). In Vitro Approaches to Model and Study Communication Between Adipose Tissue and the Liver. In: Wu, J. (eds) Thermogenic Fat. Methods in Molecular Biology, vol 1566. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-6820-6_15
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DOI: https://doi.org/10.1007/978-1-4939-6820-6_15
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Publisher Name: Humana Press, New York, NY
Print ISBN: 978-1-4939-6819-0
Online ISBN: 978-1-4939-6820-6
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