| First Author | Lee JS | Year | 2022 |
| Journal | Cell Rep | Volume | 38 |
| Issue | 8 | Pages | 110408 |
| PubMed ID | 35196497 | Mgi Jnum | J:339550 |
| Mgi Id | MGI:7520754 | Doi | 10.1016/j.celrep.2022.110408 |
| Citation | Lee JS, et al. (2022) SENP2 suppresses browning of white adipose tissues by de-conjugating SUMO from C/EBPbeta. Cell Rep 38(8):110408 |
| abstractText | The adipose tissue is a key site regulating energy metabolism. One of the contributing factors behind this is browning of white adipose tissue (WAT). However, knowledge of the intracellular determinants of the browning process remains incomplete. By generating adipocyte-specific Senp2 knockout (Senp2-aKO) mice, here we show that SENP2 negatively regulates browning by de-conjugating small ubiquitin-like modifiers from C/EBPbeta. Senp2-aKO mice are resistant to diet-induced obesity due to increased energy expenditure and heat production. Senp2 knockout promotes beige adipocyte accumulation in inguinal WAT by upregulation of thermogenic gene expression. In addition, SENP2 knockdown promotes thermogenic adipocyte differentiation of precursor cells isolated from inguinal and epididymal WATs. Mechanistically, sumoylated C/EBPbeta, a target of SENP2, suppresses expression of HOXC10, a browning inhibitor, by recruiting a transcriptional repressor DAXX. These findings indicate that a SENP2-C/EBPbeta-HOXC10 axis operates for the control of beige adipogenesis in inguinal WAT. |
