Nrf2 modulates cytosolic and mitochondrial calcium signal.
Preziuso Alessandra, Baev Artyom Y, Rustamova Fozila R, Naidu Sharadha Dayalan, Millichap Lauren, Angelova Plamena R, Lariccia Vincenzo, Dinkova-Kostova Albena T, Abramov Andrey Y
Abstract
Nrf2 is a transcription factor which regulates ∼1% of the mammalian genome and is responsible for orchestrating the cellular defense against oxidative, inflammatory and metabolic stress. Calcium (Ca2+) is a ubiquitous intracellular messenger which controls most cellular processes, from fertilization to cell death. Nrf2 and Ca2+ are involved in a large number of similar physiological processes, but it is not clear if they can regulate each other. Here, using primary co-cultures of neurons and astrocytes we asked if Nrf2 activation or deficiency alters physiological Ca2+ signaling and mitochondrial Ca2+ handling in brain cells. We found that activation of Nrf2 leads to an increase in the amplitude of Ca2+ peak and a faster Ca2+efflux in response to glutamate and ATP in neurons and astrocytes. Interestingly, Nrf2-deficient neurons and astrocytes also had higher Ca2+ peaks in response to glutamate and ATP, but the recovery in neurons was significantly delayed. Genetic (Keap1-knockdown) or pharmacological (ovameloxolone, RTA-408) activation of Nrf2 increases mitochondrial Ca2+ uptake and mitochondrial Ca2+ capacity, and this correlates with increased activity of the Na+/Ca2+/Li+ exchanger (NCLX) and inhibition of the mitochondrial permeability transition pore (mPTP). Conversely, mitochondria in neurons and astrocytes from Nrf2-knockout mice had a lower Ca2+ uptake, lower mitochondrial Ca2+ capacity and lower mitochondrial Ca2+efflux, making these cell vulnerable to Ca2+-induced cell death. Thus, Nrf2 modulates cytosolic calcium signaling and activates the mitochondrial NCLX, increasing the mitochondrial Ca2+ capacity, which adds another critical aspect to the multifaceted nature of Nrf2-mediated cytoprotection.
Key Findings
- Activation of Nrf2 increases the amplitude of cytosolic calcium peaks and accelerates calcium efflux in neurons and astrocytes.
- Nrf2 deficiency leads to higher calcium peaks but delayed recovery in neurons, indicating impaired calcium signaling.
- Nrf2 activation enhances mitochondrial calcium uptake and capacity by increasing NCLX activity and inhibiting mPTP, while Nrf2 knockout reduces these mitochondrial calcium handling capabilities, increasing vulnerability to calcium-induced cell death.
Clinical Significance
These findings highlight Nrf2's critical role in regulating calcium signaling and mitochondrial function, suggesting that modulating Nrf2 activity could protect brain cells from calcium-induced damage in oxidative stress-related neurological conditions.
Citation
Preziuso Alessandra, Baev Artyom Y, Rustamova Fozila Ret al.. Nrf2 modulates cytosolic and mitochondrial calcium signal. Redox biology. 2026-May-15.