Effect of estrogen on expression of prohibitin in white adipose tissue and liver of diet-induced obese rats
Choi, M; Chaudhari, HN; Ji, YR; Ryoo, ZY; Kim, SW; Yun, JW
HERO ID
2902041
Reference Type
Journal Article
Year
2015
Language
English
PMID
| HERO ID | 2902041 |
|---|---|
| In Press | No |
| Year | 2015 |
| Title | Effect of estrogen on expression of prohibitin in white adipose tissue and liver of diet-induced obese rats |
| Authors | Choi, M; Chaudhari, HN; Ji, YR; Ryoo, ZY; Kim, SW; Yun, JW |
| Journal | Molecular and Cellular Biochemistry |
| Volume | 407 |
| Issue | 1-2 |
| Page Numbers | 181-196 |
| Abstract | Prohibitin (PHB) is a ubiquitously expressed and highly conserved protein that participates in diverse cellular processes, and its functions are linked to a variety of diseases. In the present study, to explore transcriptional activation and signaling pathways involved in PHB regulation in response to sex hormone treatment, we investigated the effects of estrogen (17-β-estradiol, E2) on regulation of PHB in several metabolic tissues from male and female rats. Elevated expression of PHB was prominent in white adipose tissue (WAT) and the liver, and E2 stimulated PHB expression in both ND and HFD-fed rats. To further confirm the expression of PHB which was increased in WAT and the liver, we analyzed PHB expression levels in 3T3-L1 and C9 cells after the treatment of E2. Transcription and protein levels of PHB were dose-dependently increased by E2 treatment in both cell types, supporting our in vivo data. To further evaluate the possible role of E2 in elevation of PHB via estrogen receptors (ER), the potent ER inhibitor fulvestrant was treated to 3T3-L1 and C9 cells. Fulvestrant markedly suppressed both transcription and protein levels of PHB, suggesting that PHB expression in both tissues may be regulated through ERs. GeneMANIA, a predictive web interface, was used to show that Phb is regulated via the intracellular steroid hormone receptor signaling pathway, suggesting a role for ERs in expression of Phb as well as other metabolically important genes. Based on these results, we expect that targeting PHB would be a useful therapeutic approach for treatment of obesity. |
| Doi | 10.1007/s11010-015-2468-1 |
| Pmid | 26048717 |
| Wosid | WOS:000359778900019 |
| Url | http://link.springer.com/10.1007/s11010-015-2468-1 |
| Is Certified Translation | No |
| Dupe Override | No |
| Is Public | Yes |
| Language Text | English |