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Inside out: Bone marrow adipose tissue as a source of circulating adiponectin

Journal

ADIPOCYTE
Volume 5, Issue 3, Pages 251-269

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/21623945.2016.1149269

Keywords

adiponectin; anorexia nervosa; bone marrow adipose tissue; caloric restriction; lipodystrophy; obesity; white adipose tissue

Funding

  1. National Institutes of Health (USA) [K99-DE024178, T32-DK101357, R24-DK092759]
  2. Medical Research Council (UK) [MR/M021394/1]
  3. University of Edinburgh
  4. MRC [MR/M021394/1] Funding Source: UKRI
  5. Medical Research Council [MR/M021394/1] Funding Source: researchfish
  6. EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT [T32HD007505] Funding Source: NIH RePORTER
  7. NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH [R00DE024178, K99DE024178] Funding Source: NIH RePORTER
  8. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [P30DK020572] Funding Source: NIH RePORTER

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The adipocyte-derived hormone adiponectin mediates beneficial cardiometabolic effects, and hypoadiponectinemia is a biomarker for increased metabolic and cardiovascular risk. Indeed, circulating adiponectin decreases in obesity and insulin-resistance, likely because of impaired production from white adipose tissue (WAT). Conversely, lean states such as caloric restriction (CR) are characterized by hyperadiponectinemia, even without increased adiponectin production from WAT. The reasons underlying this paradox have remained elusive, but our recent research suggests that CR-associated hyperadiponectinemia derives from an unexpected source: bone marrow adipose tissue (MAT). Herein, we elaborate on this surprising discovery, including further discussion of potential mechanisms influencing adiponectin production from MAT; additional evidence both for and against our conclusions; and observations suggesting that the relationship between MAT and adiponectin might extend beyond CR. While many questions remain, the burgeoning study of MAT promises to reveal further key insights into MAT biology, both as a source of adiponectin and beyond.

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