Please use this identifier to cite or link to this item: https://hdl.handle.net/11147/12315
Title: The role of cycloastragenol at the intersection of NRF2/ARE, telomerase, and proteasome activity
Authors: Yılmaz, Sinem
Bedir, Erdal
Ballar Kırmızıbayrak, Petek
Ege Üniversitesi
01. Izmir Institute of Technology
Ege Üniversitesi
Keywords: Aging
Cycloastragenol
Neuroprotection
Oxidative stress
Telomerase
Issue Date: Aug-2022
Publisher: Elsevier
Abstract: Aging is well-characterized by the gradual decline of cellular functionality. As redox balance, proteostasis, and telomerase systems have been found to be associated with aging and age-related diseases, targeting these systems with small compounds has been considered a promising therapeutic approach. Cycloastragenol (CA), a small molecule telomerase activator obtained from Astragalus species, has been reported to positively affect several age-related pathophysiologies, but the mechanisms underlying CA activity have yet to be reported. Here, we presented that CA increased NRF2 nuclear localization and activity leading to upregulation of cytoprotective enzymes and attenuation of oxidative stress-induced ROS levels. Furthermore, CA-mediated induction of telomerase activity was found to be regulated by NRF2. CA not only increased the expression of hTERT but also its nuclear localization via upregulating the Hsp90-chaperon complex. In addition to modulating nuclear hTERT levels at unstressed conditions, CA alleviated oxidative stress-induced mitochondrial hTERT levels while increasing nuclear hTERT levels. Concomitantly, H2O2-induced mitochondrial ROS level was found to be significantly decreased by CA administration. Our data also revealed that CA strongly enhanced proteasome activity and assembly. More importantly, the proteasome activator effect of CA is dependent on the induction of telomerase activity, which is mediated by NRF2 system. In conclusion, our results not only revealed the cross-talk among NRF2, telomerase, and proteasome systems but also that CA functions at the intersection of these three major aging-related cellular pathways.
Description: This study was supported by Scientific and Technological Research Council of Turkey (TUBITAK, Grant number: 119Z086)
URI: https://doi.org/10.1016/j.freeradbiomed.2022.06.230
https://hdl.handle.net/11147/12315
Appears in Collections:Bioengineering / Biyomühendislik
PubMed İndeksli Yayınlar Koleksiyonu / PubMed Indexed Publications Collection
Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
WoS İndeksli Yayınlar Koleksiyonu / WoS Indexed Publications Collection

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