Journal
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
Volume 22, Issue 8, Pages -Publisher
MDPI
DOI: 10.3390/ijms22084172
Keywords
renal proximal tubule; mitochondria; membrane transport; glutathione; biomarkers; oxidative stress; nephrotoxicity
Funding
- Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI, USA
- NIDDK [R01-DK40725]
Ask authors/readers for more resources
Mitochondria in renal proximal tubular cells play various key roles, including ATP synthesis, regulation of redox status, initiation of mitophagy and apoptosis. The membrane transport mechanisms of glutathione and its derivatives across the mitochondrial inner membrane are critical for these functions and may serve as targets for therapeutic approaches. Detecting specific components released by renal mitochondria into urine or extracellular medium could serve as indicators of exposure to nephrotoxicants before irreversible renal injury occurs.
Mitochondria are well-known to function as the primary sites of ATP synthesis in most mammalian cells, including the renal proximal tubule. Other functions have also been associated with different mitochondrial activities, including the regulation of redox status and the initiation of mitophagy and apoptosis. Mechanisms for the membrane transport of glutathione (GSH) and various GSH-derived metabolites across the mitochondrial inner membrane of renal proximal tubular cells are critical determinants of these functions and may serve as pharmacological targets for potential therapeutic approaches. Specific interactions of reactive intermediates, derived from drug metabolism, with molecular components in mitochondria have been identified as early steps in diverse forms of chemically-induced nephrotoxicity. Applying this key observation, we developed a novel hypothesis regarding the identification of early, sensitive, and specific biomarkers of exposure to nephrotoxicants. The underlying concept is that upon exposure to a diverse array of environmental contaminants, as well as therapeutic drugs whose efficacy is limited by nephrotoxicity, renal mitochondria will release both high- and low-molecular-weight components into the urine or the extracellular medium in an in vitro model. The detection of these components may then serve as indicators of exposure before irreversible renal injury has occurred.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available