4.7 Article

The conserved Mediator subunit cyclin C (CCNC) is required for brown adipocyte development and lipid accumulation

Journal

MOLECULAR METABOLISM
Volume 64, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.molmet.2022.101548

Keywords

CCNC; brown fat; Lipid droplet; Progenitor; Proliferation; Lipogenesis

Funding

  1. National Institutes of Health [P30 DK020541, DK098439, DK117417, DK110063]
  2. Natural Science Foundation of Guangxi Province [2020GXNSFAA297043]
  3. Youth Science Foundation of National Natural Science Foundation of China [82100913]

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CCNC-Mediator plays an important role in the development of brown adipose tissue (BAT) and lipid accumulation in brown adipocytes. Conditional knock-out of CCNC gene leads to BAT paucity and affects brown adipose tissue development and cell proliferation, but not cell death. CCNC in brown adipocytes regulates the expression of lipogenic genes through the C/EBP alpha/GLUT4/ChREBP pathway.
Objective: Cyclin C (CCNC) is the most conserved subunit of the Mediator complex, which is an important transcription cofactor. Recently, we have found that CCNC facilitates brown adipogenesis in vitro by activating C/EBP alpha-dependent transcription. However, the role of CCNC in brown adipose tissue (BAT) in vivo remains unclear. Methods: We generated conditional knock-out mice by crossing Ccnc(flox/flox) mice with Myf5(Cre), Ucp1(Cre) or Adipoq(Cre) transgenic mice to investigate the role of CCNC in BAT development and function. We applied glucose and insulin tolerance test, cold exposure and indirect calorimetry to capture the physiological phenotypes and used immunostaining, immunoblotting, qRT-PCR, RNA-seq and cell culture to elucidate the underlying mechanisms. Results: Here, we show that deletion of CCNC in Myf5(+) progenitor cells caused BAT paucity, despite the fact that there was significant neonatal lethality. Mechanistically different from in vitro, CCNC deficiency impaired the proliferation of embryonic brown fat progenitor cells without affecting brown adipogenesis or cell death. Interestingly, CCNC deficiency robustly reduced age-dependent lipid accumulation in differentiated brown adipocytes in all three mouse models. Mechanistically, CCNC in brown adipocytes is required for lipogenic gene expression through the activation of the C/EBP alpha/GLUT4/ChREBP axis. Consistent with the importance of de novo lipogenesis under carbohydrate-rich diets, high-fat diet (HFD) feeding abolished CCNC deficiency -caused defects of lipid accumulation in BAT. Although insulin sensitivity and response to acute cold exposure were not affected, CCNC deficiency in Ucp1(+) cells enhanced the browning of white adipose tissue (beiging) upon prolonged cold exposure. Conclusions: Together, these data indicate an important role of CCNC-Mediator in the regulation of BAT development and lipid accumulation in brown adipocytes. (C) 2022 The Authors. Published by Elsevier GmbH.

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