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Nuclear factor erythroid 2 related Factor-1 is stimulated by the nutraceutical celastrol at proteasome inhibiting
Alireza Ahadiabhari1, Lei Li1, Shennan Su1
1Department of Anatomy, Physiology, and Pharmacology, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Abstract:
The mechanism by which many nutraceuticals promote health is incompletely understood. Some act by inhibiting the proteasome. Nuclear Factor Erythroid 2 Related Factor 1 (NRF1) is a stress-protective transcription factor that is stimulated by suppressed proteasome activity, such as upon exposure to proteasome inhibitor. Here, we investigated whether nutraceutical compounds with proteasome inhibitory properties stimulate NRF1 to regulate stress-protective genes. Using a luciferase-based promoter reporting the activity of NRF1 and its homolog NRF2 in Hepa 1-6 cells, we performed a small nutraceutical screen and identified that 2 and 4 μM treatment with celastrol exhibited robust stimulatory effect. Using the same reporter in wild type and gene deleted murine embryonic fibroblasts, we found that Nrf1 deficiency reduced celastrol-stimulated luciferase activity. In Hep3B cells, we found that 2 μM celastrol, but not lower concentrations, increased NRF1 processing and nuclear accumulation while also suppressing trypsin-like, chymotrypsin-like, and caspase-like activities of the proteasome, similar to proteasome inhibiting drugs. However, using control and NRF1 deficient Hep3B cells treated with 2 μM celastrol, MG132, bortezomib, or vehicle, we found distinct effects by celastrol versus MG132 and bortezomib on NRF1-dependent regulation of stress-protective genes. Our results show that celastrol can stimulate NRF1 at concentrations that suppress proteasome activity, but its effect on gene regulation is distinct compared to proteasome inhibitor. Overall, our findings reveal that NRF1 may play a role in the health promoting effects of celastrol and possibly other nutraceuticals with proteasome inhibitory properties.
Insights
Celastrol stimulates the stress-protective factor Nuclear Factor Erythroid 2 Related Factor 1 (NRF1) by inhibiting proteasome activity. However, celastrol
Area of Science:
- Molecular Biology
- Cell Biology
- Pharmacology
Background:
- The health benefits of many nutraceuticals are not fully understood, with some acting via proteasome inhibition.
- Nuclear Factor Erythroid 2 Related Factor 1 (NRF1) is a transcription factor activated by suppressed proteasome activity.
Purpose of the Study:
- To investigate if nutraceuticals with proteasome inhibitory properties stimulate NRF1.
- To determine if celastrol, a nutraceutical compound, activates NRF1 and regulates stress-protective genes.
Main Methods:
- Utilized a luciferase-based reporter assay in Hepa 1-6 cells to screen nutraceuticals for NRF1 and NRF2 activity.
- Employed wild-type and Nrf1-deficient murine embryonic fibroblasts and Hep3B cells to assess celastrol's effects.
- Measured proteasome activity and NRF1 processing, nuclear accumulation, and downstream gene regulation.
Main Results:
- Celastrol at 2 and 4 μM robustly stimulated NRF1 activity in Hepa 1-6 cells.
- Nrf1 deficiency attenuated celastrol-induced reporter activity in murine embryonic fibroblasts.
- Celastrol (2 μM) increased NRF1 processing and nuclear accumulation in Hep3B cells, suppressing proteasome activity.
- Celastrol demonstrated distinct NRF1-dependent gene regulation compared to proteasome inhibitors like MG132 and bortezomib.
Conclusions:
- Celastrol stimulates NRF1 at concentrations that inhibit proteasome activity.
- Celastrol's regulation of stress-protective genes differs from that of traditional proteasome inhibitors.
- NRF1 may mediate some health benefits of celastrol and other proteasome-inhibiting nutraceuticals.
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