Bone Marrow Adipose Tissue Is an Endocrine Organ that Contributes to Increased Circulating Adiponectin during Caloric Restriction

William P. Cawthorn*, Erica L. Scheller, Brian S. Learman, Sebastian D. Parlee, Becky R. Simon, Hiroyuki Mori, Xiaomin Ning, Adam J. Bree, Benjamin Schell, David T. Broome, Sandra S. Soliman, Jenifer L. DelProposto, Carey N. Lumeng, Aditi Mitra, Sandeep V. Pandit, Katherine A. Gallagher, Joshua D. Miller, Venkatesh Krishnan, Susanta K. Hui, Miriam A. BredellaPouneh K. Fazeli, Anne Klibanski, Mark C. Horowitz, Clifford J. Rosen, Ormond A. MacDougald

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

The adipocyte-derived hormone adiponectin promotes metabolic and cardiovascular health. Circulating adiponectin increases in lean states such as caloric restriction (CR), but the reasons for this paradox remain unclear. Unlike white adipose tissue (WAT), bone marrow adipose tissue (MAT) increases during CR, and both MAT and serum adiponectin increase in many other clinical conditions. Thus, we investigated whether MAT contributes to circulating adiponectin. We find that adiponectin secretion is greater from MAT than WAT. Notably, specific inhibition of MAT formation in mice results in decreased circulating adiponectin during CR despite unaltered adiponectin expression in WAT. Inhibiting MAT formation also alters skeletal muscle adaptation to CR, suggesting that MAT exerts systemic effects. Finally, we reveal that both MAT and serum adiponectin increase during cancer therapy in humans. These observations identify MAT as an endocrine organ that contributes significantly to increased serum adiponectin during CR and perhaps in other adverse states.

Original languageEnglish
Pages (from-to)368-375
Number of pages8
JournalCell Metabolism
Volume20
Issue number2
Early online date3 Jul 2014
DOIs
Publication statusPublished - 5 Aug 2014

Keywords / Materials (for Non-textual outputs)

  • ANOREXIA-NERVOSA
  • METABOLISM
  • EXPRESSION
  • MICE
  • PROTEIN
  • DIET
  • DIFFERENTIATION
  • MITOCHONDRIAL
  • PREGNANCY
  • GLUCOSE

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