| Literature DB >> 31668873 |
Atul S Deshmukh1, Lone Peijs2, Jacqueline L Beaudry3, Naja Z Jespersen4, Carsten H Nielsen5, Tao Ma6, Andreas D Brunner7, Therese J Larsen4, Rafael Bayarri-Olmos8, Bhargav S Prabhakar9, Charlotte Helgstrand10, Mai C K Severinsen4, Birgitte Holst11, Andreas Kjaer12, Mads Tang-Christensen10, Annika Sanfridson10, Peter Garred8, Gilbert G Privé13, Bente K Pedersen4, Zachary Gerhart-Hines6, Søren Nielsen4, Daniel J Drucker3, Matthias Mann14, Camilla Scheele15.
Abstract
Adipokines secreted from white adipose tissue play a role in metabolic crosstalk and homeostasis, whereas the brown adipose secretome is less explored. We performed high-sensitivity mass-spectrometry-based proteomics on the cell media of human adipocytes derived from the supraclavicular brown adipose and from the subcutaneous white adipose depots of adult humans. We identified 471 potentially secreted proteins covering interesting categories such as hormones, growth factors, extracellular matrix proteins, and proteins of the complement system, which were differentially regulated between brown and white adipocytes. A total of 101 proteins were exclusively quantified in brown adipocytes, and among these was ependymin-related protein 1 (EPDR1). EPDR1 was detected in human plasma, and functional studies suggested a role for EPDR1 in thermogenic determination during adipogenesis. In conclusion, we report substantial differences between the secretomes of brown and white human adipocytes and identify novel candidate batokines that can be important regulators of human metabolism.Entities:
Keywords: adipocyte complement factors; adipokines; brown fat commitment; brown fat differentiation; extracellular matrix proteins; human batokines; human brown adipocytes; human brown fat; mitochondria; secretomics
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Year: 2019 PMID: 31668873 DOI: 10.1016/j.cmet.2019.10.001
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287