Exercise training remodels inguinal white adipose tissue through adaptations in innervation, vascularization, and the extracellular matrix

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  • Pasquale Nigro
  • Maria Vamvini
  • Jiekun Yang
  • Tiziana Caputo
  • Li Lun Ho
  • Nicholas P. Carbone
  • Danae Papadopoulos
  • Royce Conlin
  • Jie He
  • Michael F. Hirshman
  • Joseph D. White
  • Jacques Robidoux
  • Robert C. Hickner
  • Søren Nielsen
  • Pedersen, Bente Klarlund
  • Manolis Kellis
  • Roeland J.W. Middelbeek
  • Laurie J. Goodyear
Inguinal white adipose tissue (iWAT) is essential for the beneficial effects of exercise training on metabolic health. The underlying mechanisms for these effects are not fully understood, and here, we test the hypothesis that exercise training results in a more favorable iWAT structural phenotype. Using biochemical, imaging, and multi-omics analyses, we find that 11 days of wheel running in male mice causes profound iWAT remodeling including decreased extracellular matrix (ECM) deposition and increased vascularization and innervation. We identify adipose stem cells as one of the main contributors to training-induced ECM remodeling, show that the PRDM16 transcriptional complex is necessary for iWAT remodeling and beiging, and discover neuronal growth regulator 1 (NEGR1) as a link between PRDM16 and neuritogenesis. Moreover, we find that training causes a shift from hypertrophic to insulin-sensitive adipocyte subpopulations. Exercise training leads to remarkable adaptations to iWAT structure and cell-type composition that can confer beneficial changes in tissue metabolism.
OriginalsprogEngelsk
Artikelnummer112392
TidsskriftCell Reports
Vol/bind42
Udgave nummer4
Antal sider22
ISSN2211-1247
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This work was supported by NIH grants R01DK099511 and R01DK101043 (to L.J.G.); K23DK114550 (to R.J.W.M.); T32DK00726042 , F32DK12643201 , and Joslin DRC Pilot and Feasibility Program award (to M.V.); and the Joslin Diabetes Center DRC ( P30 DK36836 ). The Center for Physical Activity Research (CFAS) is supported by TrygFonden (grant IDs 101390 , 20045 , and 125132 ). The Center of Inflammation and Metabolism (CIM) was supported by a grant from the Danish National Research Foundation ( DNRF55 ). We thank Dr. Krithika Ramachandran and Madison M. Columbus for scientific feedback, Drs. Michael R. Blanchard and Mahmoud EL-Rifai for technical assistance with Adipo-Clear image acquisition, and Drs. Hui Pan and Jonathan M. Dreyfuss for statistical analysis support.

Publisher Copyright:
© 2023 The Authors

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