17β-Oestradiol Attenuates the Photoreceptor Apoptosis in Mice with Retinitis Pigmentosa by Regulating N-myc Downstream Regulated Gene 2 Expression

• Published in: Neuroscience 2021-01, Vol.452, p.280-294
• Main Authors: Xiong, Ye-Cheng, Chen, Tao, Yang, Xiao-Bei, Deng, Chun-Lei, Ning, Qi-Lan, Quan, Rui, Yu, Xiao-Rui
• Format: Article
• Language: English
• Subjects: 17β-oestradiol; Animals; Apoptosis; Disease Models, Animal; Estradiol - pharmacology; Mice; N-myc downstream regulated gene 2; Photoreceptor Cells; Photoreceptor Cells, Vertebrate; photoreceptors; Retinal Degeneration; retinitis pigmentosa; Retinitis Pigmentosa - drug therapy
• ISSN: 0306-4522; 1873-7544
• DOI: 10.1016/j.neuroscience.2020.11.010

•βE2 reduces the apoptosis of photoreceptor cells in RP models.•βE2 protects photoreceptor cells against apoptosis in RP models by maintaining NDRG2 expression.•βE2 may regulate NDRG2 expression in RP models via a classic ER-mediated mechanism. Retinitis pigmentosa (RP) is a heterogeneous group of retinal degenerative diseases in which the final pathological feature is photoreceptor cell apoptosis. Currently, the pathogenesis of RP remains poorly understood and therapeutics are ineffective. 17β-Oestradiol (βE2) is universally acknowledged as a neuroprotective factor in neurodegenerative diseases and has manifested neuroprotective effects in a light-induced retinal degeneration model. Recently, we identified N-myc downstream regulated gene 2 (NDRG2) suppression as a molecular marker of mouse retinal photoreceptor-specific cell death. βE2 has also been reported to regulate NDRG2 in salivary acinar cells. Therefore, in this study, we investigated whether βE2 plays a protective role in RP and regulates NDRG2 in photoreceptor cells. To this end, we generated RP models and observed that βE2 not only reduced the apoptosis of photoreceptor cells, but also restored the level of NDRG2 expression in RP models. Then, we showed that siNDRG2 inhibits the anti-apoptotic effect of βE2 on photoreceptor cells in a cellular RP model. Subsequently, we used a classic oestrogen receptor (ER) antagonist to attenuate the effects of βE2, suggesting that βE2 exerted its effects on RP models via the classic ERs. In addition, we performed a bioinformatics analysis, and the results indicated that the reported oestrogen response element (ERE) sequence is present in the promoter region of the mouse NDRG2 gene. Overall, our results suggest that βE2 attenuated the apoptosis of photoreceptor cells in RP models by maintaining NDRG2 expression via a classic ER-mediated mechanism.