Spatial and temporal control of mitochondrial H2O2 release in intact human cells. (11th February 2022)
- Record Type:
- Journal Article
- Title:
- Spatial and temporal control of mitochondrial H2O2 release in intact human cells. (11th February 2022)
- Main Title:
- Spatial and temporal control of mitochondrial H2O2 release in intact human cells
- Authors:
- Hoehne, Michaela Nicole
Jacobs, Lianne J H C
Lapacz, Kim Jasmin
Calabrese, Gaetano
Murschall, Lena Maria
Marker, Teresa
Kaul, Harshita
Trifunovic, Aleksandra
Morgan, Bruce
Fricker, Mark
Belousov, Vsevolod V
Riemer, Jan - Abstract:
- Abstract: Hydrogen peroxide (H2 O2 ) has key signaling roles at physiological levels, while causing molecular damage at elevated concentrations. H2 O2 production by mitochondria is implicated in regulating processes inside and outside these organelles. However, it remains unclear whether and how mitochondria in intact cells release H2 O2 . Here, we employed a genetically encoded high‐affinity H2 O2 sensor, HyPer7, in mammalian tissue culture cells to investigate different modes of mitochondrial H2 O2 release. We found substantial heterogeneity of HyPer7 dynamics between individual cells. We further observed mitochondria‐released H2 O2 directly at the surface of the organelle and in the bulk cytosol, but not in the nucleus or at the plasma membrane, pointing to steep gradients emanating from mitochondria. Gradient formation is controlled by cytosolic peroxiredoxins, which act redundantly and with a substantial reserve capacity. Dynamic adaptation of cytosolic thioredoxin reductase levels during metabolic changes results in improved H2 O2 handling and explains previously observed differences between cell types. Our data suggest that H2 O2 ‐mediated signaling is initiated only in close proximity to mitochondria and under specific metabolic conditions. Synopsis: Mitochondria are main producers of H2 O2 in cells and its release is an important indicator of their functional state. Here, nutrients affecting mitochondrial metabolism and cytosolic antioxidative systems are found toAbstract: Hydrogen peroxide (H2 O2 ) has key signaling roles at physiological levels, while causing molecular damage at elevated concentrations. H2 O2 production by mitochondria is implicated in regulating processes inside and outside these organelles. However, it remains unclear whether and how mitochondria in intact cells release H2 O2 . Here, we employed a genetically encoded high‐affinity H2 O2 sensor, HyPer7, in mammalian tissue culture cells to investigate different modes of mitochondrial H2 O2 release. We found substantial heterogeneity of HyPer7 dynamics between individual cells. We further observed mitochondria‐released H2 O2 directly at the surface of the organelle and in the bulk cytosol, but not in the nucleus or at the plasma membrane, pointing to steep gradients emanating from mitochondria. Gradient formation is controlled by cytosolic peroxiredoxins, which act redundantly and with a substantial reserve capacity. Dynamic adaptation of cytosolic thioredoxin reductase levels during metabolic changes results in improved H2 O2 handling and explains previously observed differences between cell types. Our data suggest that H2 O2 ‐mediated signaling is initiated only in close proximity to mitochondria and under specific metabolic conditions. Synopsis: Mitochondria are main producers of H2 O2 in cells and its release is an important indicator of their functional state. Here, nutrients affecting mitochondrial metabolism and cytosolic antioxidative systems are found to modulate H2 O2 gradients and signaling in intact human cells. Mitochondrial H2 O2 can be detected in the cytosol in intact human cells, but not the nucleus or at the plasma membrane. Mitochondrial H2 O2 gradients are steep and controlled by peroxiredoxins 1 and 2. Peroxiredoxins 1 and 2 complement each other and are present with a substantial reserve capacity. Metabolism‐induced changes of reducing processes control peroxiredoxin activity. Abstract : A genetically‐encoded sensor shows how peroxiredoxins and thioredoxin reductase restrict H2 O2 signaling to the proximity of mitochondria and specific metabolic conditions. … (more)
- Is Part Of:
- EMBO journal. Volume 41:Number 7(2022)
- Journal:
- EMBO journal
- Issue:
- Volume 41:Number 7(2022)
- Issue Display:
- Volume 41, Issue 7 (2022)
- Year:
- 2022
- Volume:
- 41
- Issue:
- 7
- Issue Sort Value:
- 2022-0041-0007-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2022-02-11
- Subjects:
- hydrogen peroxide release -- HyPer7 -- mitochondria -- peroxiredoxin
Molecular biology -- Periodicals
572.805 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.15252/embj.2021109169 ↗
- Languages:
- English
- ISSNs:
- 0261-4189
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3733.085000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21295.xml