Clock represses preadipocytes adipogenesis via GILZ. Issue 8 (27th February 2018)
- Record Type:
- Journal Article
- Title:
- Clock represses preadipocytes adipogenesis via GILZ. Issue 8 (27th February 2018)
- Main Title:
- Clock represses preadipocytes adipogenesis via GILZ
- Authors:
- Zhu, Zhu
Xu, Lirong
Cai, Tingting
Yuan, Gongsheng
Sun, Ning
Lu, Chao
Qian, Ruizhe - Abstract:
- Abstract : Adiposity is a worldwide health threat that needs to be prevented. Circadian gene Clock (circadian locomotor output cycles kaput) is closely correlated to adiposity; for example, weight gain, adipocytes size expansion, and serum lipid level rise in Clock Δ19 mice compared to C57BL/6J mice. However, the precise role of Clock during adipogenic differentiation is unknown. Herein, the circadian gene Clock is shown to regulate adipogenesis mediated by GILZ. Clock ‐mediated attenuation and upregulation influenced lipid synthesis and affected the levels of adipogenic transcriptional factors, C/EBP‐β, C/EBP‐α, PPAR‐γ, and FABP4, both in vivo and in vitro (primary adipose‐derived stromal cells and 3T3‐L1 cells). Chromatin immunoprecipitation (ChIP) assay, reporter gene assay, and serum shock assay found that Clock transcriptionally regulated the glucocorticoid‐induced leucine zipper (GILZ). Furthermore, GILZ attenuation could relieve the inhibitory effect of Clock on lipid synthesis and GILZ overexpression also reduced the promotion role of Clock attenuation in adipogenesis suggesting that Clock inhibits adipogenic differentiation of preadipocytes via GILZ. The current results demonstrate how circadian genes are likely to regulate adiposity, affecting the adipogenic differentiation process, as well as, increasing the fat cells number. Therefore, this study may provide novel insights into the underlying mechanism explaining the correlation between Clock mutation andAbstract : Adiposity is a worldwide health threat that needs to be prevented. Circadian gene Clock (circadian locomotor output cycles kaput) is closely correlated to adiposity; for example, weight gain, adipocytes size expansion, and serum lipid level rise in Clock Δ19 mice compared to C57BL/6J mice. However, the precise role of Clock during adipogenic differentiation is unknown. Herein, the circadian gene Clock is shown to regulate adipogenesis mediated by GILZ. Clock ‐mediated attenuation and upregulation influenced lipid synthesis and affected the levels of adipogenic transcriptional factors, C/EBP‐β, C/EBP‐α, PPAR‐γ, and FABP4, both in vivo and in vitro (primary adipose‐derived stromal cells and 3T3‐L1 cells). Chromatin immunoprecipitation (ChIP) assay, reporter gene assay, and serum shock assay found that Clock transcriptionally regulated the glucocorticoid‐induced leucine zipper (GILZ). Furthermore, GILZ attenuation could relieve the inhibitory effect of Clock on lipid synthesis and GILZ overexpression also reduced the promotion role of Clock attenuation in adipogenesis suggesting that Clock inhibits adipogenic differentiation of preadipocytes via GILZ. The current results demonstrate how circadian genes are likely to regulate adiposity, affecting the adipogenic differentiation process, as well as, increasing the fat cells number. Therefore, this study may provide novel insights into the underlying mechanism explaining the correlation between Clock mutation and adiposity. Abstract : The circadian gene Clock is shown to regulate adipogenesis. And Clock transcriptionally regulated the glucocorticoid‐induced leucine zipper. … (more)
- Is Part Of:
- Journal of cellular physiology. Volume 233:Issue 8(2018:Aug.)
- Journal:
- Journal of cellular physiology
- Issue:
- Volume 233:Issue 8(2018:Aug.)
- Issue Display:
- Volume 233, Issue 8 (2018)
- Year:
- 2018
- Volume:
- 233
- Issue:
- 8
- Issue Sort Value:
- 2018-0233-0008-0000
- Page Start:
- 6028
- Page End:
- 6040
- Publication Date:
- 2018-02-27
- Subjects:
- 3T3‐L1 preadipocyte -- adipogenesis -- adipose tissue‐derived stem cells -- Clock -- glucocorticoid‐induced leucine zipper
Physiology -- Periodicals
Cell physiology -- Periodicals
571.6 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/jcp.26420 ↗
- Languages:
- English
- ISSNs:
- 0021-9541
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4955.020000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 23392.xml