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Activation of PPARγ induces profound multilocularization of adipocytes in adult mouse white adipose tissues

  • Young Jun Koh
  • , Byung Hyun Park
  • , Ji Hyun Park
  • , Jinah Han
  • , In Kyu Lee
  • , Jin Woo Park
  • , Gou Young Koh
  • Korea Advanced Institute of Science and Technology
  • Jeonbuk National University
  • Kyungpook National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

We sought to determine the effects of activation of peroxisome proliferator-activated receptor-γ (PPAR-γ) on multilocularization of adipocytes in adult white adipose tissue (WAT). Male C57BL/6 normal, db/db, and ob/ob mice were treated with agonists of PPAR-γ, PPAR-α, or β3-adrenoceptor for 3 weeks. To distinguish multilocular adipocytes from unilocular adipocytes, wholemounted adipose tissues were co-immunostained for perilipin and collagen IV. PPAR-γ activation with rosiglitazone or pioglitazone induced a profound change of unilocular adipocytes into smaller, multilocular adipocytes in adult WAT in a time-dependent, dose-dependent, and reversible manner. PPAR-α activation with fenofibrate did not affect the number of locules or remodeling. db/db and ob/ob obese mice exhibited less multilocularization in response to PPAR-γ activation compared to normal mice. Nevertheless, all adipocytes activated by PPAR-γ contained a single nucleus regardless of locule number. Multilocular adipocytes induced by PPAR-γ activation contained substantially increased mitochondrial content and enhanced expression of uncoupling protein-1, PPAR-γ coactivator-1-α, and perilipin. Taken together, PPAR-γ activation induces profound multilocularization and enhanced mitochondrial biogenesis in the adipocytes of adult WAT. These changes may affect the overall function of WAT.

Original languageEnglish
Pages (from-to)880-895
Number of pages16
JournalExperimental and Molecular Medicine
Volume41
Issue number12
DOIs
StatePublished - 2009.12.31

Keywords

  • Mitochondria
  • Mitochondrial uncoupling protein
  • Pioglitazone
  • Receptors, adrenergic, β-3
  • Rosiglitazone

Quacquarelli Symonds(QS) Subject Topics

  • Medicine
  • Biological Sciences

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