| First Author | Zhu Z | Year | 2018 |
| Journal | J Cell Physiol | Volume | 233 |
| Issue | 8 | Pages | 6028-6040 |
| PubMed ID | 29278648 | Mgi Jnum | J:313206 |
| Mgi Id | MGI:6791627 | Doi | 10.1002/jcp.26420 |
| Citation | Zhu Z, et al. (2018) Clock represses preadipocytes adipogenesis via GILZ. J Cell Physiol 233(8):6028-6040 |
| abstractText | 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(Delta19) 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-beta, C/EBP-alpha, PPAR-gamma, 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. |
