4.8 Article

Proteomics-Based Comparative Mapping of the Secretomes of Human Brown and White Adipocytes Reveals EPDR1 as a Novel Batokine

Journal

CELL METABOLISM
Volume 30, Issue 5, Pages 963-+

Publisher

CELL PRESS
DOI: 10.1016/j.cmet.2019.10.001

Keywords

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Funding

  1. TrygFonden [101390, 20045]
  2. Danish National Research Foundation [DNRF55]
  3. Danish Council for Strategic Research [09-067009, 09075724]
  4. Novo Nordisk Foundation [NNF18CC0034900, NNF14CC001, NNF18OC0034378]
  5. Max-Planck-Society for the Advancement of Science
  6. Banting and Best Diabetes Centre-Novo Nordisk Chair in Incretin Biology
  7. CIHR operating grant [154321]
  8. European Research Council (ERC) under the European Union's Horizon 2020 Research and Innovation Programme [639382]
  9. Danish Diabetes Academy - Novo Nordisk Foundation [DFF-6110-00489]
  10. Novo Nordisk A/S
  11. Danish Research Foundation of Independent Research [DFF-6110-00489]
  12. European Research Council (ERC) [639382] Funding Source: European Research Council (ERC)

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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.

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