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Mitochondrial Glutathione: Regulation and Functions

Journal

ANTIOXIDANTS & REDOX SIGNALING
Volume 27, Issue 15, Pages 1162-1177

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/ars.2017.7121

Keywords

glutathione; mitochondria; genetically encoded sensors

Funding

  1. German research council (DFG) [RI2150/1-2, RI2150/2-1 [SPP1710], SFB1218 TP B02]
  2. Forschungsinitiative Rheinland-Pfalz BioComp
  3. University of Kaiserslautern Nachwuchsring
  4. DFG [SPP1710 (MO 2774/2-1)]

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Significance: Mitochondrial glutathione fulfills crucial roles in a number of processes, including iron-sulfur cluster biosynthesis and peroxide detoxification. Recent Advances: Genetically encoded fluorescent probes for the glutathione redox potential (E-GSH) have permitted extensive new insights into the regulation of mitochondrial glutathione redox homeostasis. These probes have revealed that the glutathione pools of the mitochondrial matrix and intermembrane space (IMS) are highly reduced, similar to the cytosolic glutathione pool. The glutathione pool of the IMS is in equilibrium with the cytosolic glutathione pool due to the presence of porins that allow free passage of reduced glutathione (GSH) and oxidized glutathione (GSSG) across the outer mitochondrial membrane. In contrast, limited transport of glutathione across the inner mitochondrial membrane ensures that the matrix glutathione pool is kinetically isolated from the cytosol and IMS. Critical Issues: In contrast to the situation in the cytosol, there appears to be extensive crosstalk between the mitochondrial glutathione and thioredoxin systems. Further, both systems appear to be intimately involved in the removal of reactive oxygen species, particularly hydrogen peroxide (H2O2), produced in mitochondria. However, a detailed understanding of these interactions remains elusive. Future Directions: We postulate that the application of genetically encoded sensors for glutathione in combination with novel H2O2 probes and conventional biochemical redox state assays will lead to fundamental new insights into mitochondrial redox regulation and reinvigorate research into the physiological relevance of mitochondrial redox changes.

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