Tfe3 and Tfeb Transcriptionally Regulate Peroxisome Proliferator-Activated Receptor γ2 Expression in Adipocytes and Mediate Adiponectin and Glucose Levels in Mice

• Published in: Molecular and cellular biology Vol. 37; no. 15
• Main Authors: Salma, Nunciada, Song, Jun S., Kawakami, Akinori, Devi, Suprabha P., Khaled, Mehdi, Cacicedo, José M., Fisher, David E.
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 01.08.2017; American Society for Microbiology
• Subjects: 3T3-L1 Cells; adipocyte; Adipogenesis; Adiponectin; Animals; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - analysis; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism; development; Energy Metabolism; Female; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; PPAR gamma - genetics; Pparγ; Promoter Regions, Genetic; Tfe3; Tfe3KO mouse; Tfeb; transcription; Transcriptional Activation; Up-Regulation; Tfe3KO mouse; development; transcription; Tfe3; adipocyte; Tfeb; Pparγ
• ISSN: 1098-5549; 0270-7306; 1098-5549
• DOI: 10.1128/MCB.00608-16

Members of the MiT transcription factor family are pivotal regulators of several lineage-selective differentiation programs. We show that two of these, Tfeb and Tfe3, control the regulator of adipogenesis, peroxisome proliferator-activated receptor γ2 (Pparγ2). Knockdown of Tfeb or Tfe3 expression during in vitro adipogenesis causes dramatic downregulation of Pparγ2 expression as well as adipogenesis. Additionally, we found that these factors regulate Pparγ2 in mature adipocytes. Next, we demonstrated that Tfeb and Tfe3 act directly by binding to consensus E-boxes within the Pparγ transcriptional regulatory region. This transcriptional control also exists in vivo, as we discovered that wild-type mice in the fed state increased their expression of Tfe3, Tf3b, and Pparγ in white adipose tissue. Furthermore, Tfe3 knockout (Tfe3KO) mice in the fed state failed to upregulate Pparγ and the adiponectin gene, a Pparγ-dependent gene, confirming the in vivo role for Tfe3. Lastly, we found that blood glucose is elevated and serum adiponectin levels are suppressed in the Tfe3KO mice, indicating that the Tfe3/Tfeb/Pparγ2 axis may contribute to whole-body energy balance. Thus, we offer new insights into the upstream regulation of Pparγ by Tfe3/Tf3b and propose that targeting these transcription factors may offer opportunities to complement existing approaches for the treatment of diseases that have dysregulated energy metabolism.