Evolutionarily Conserved Role of Thioredoxin Systems in Determining Longevity

Thioredoxin and thioredoxin reductase are evolutionarily conserved antioxidant enzymes that protect organisms from oxidative stress. These proteins also play roles in redox signaling and can act as a redox-independent cellular chaperone. In most organisms, there is a cytoplasmic and mitochondrial th...

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Bibliographic Details
Main Authors: Abdelrahman AlOkda (Author), Jeremy M. Van Raamsdonk (Author)
Format: Book
Published: MDPI AG, 2023-04-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Abdelrahman AlOkda  |e author 
700 1 0 |a Jeremy M. Van Raamsdonk  |e author 
245 0 0 |a Evolutionarily Conserved Role of Thioredoxin Systems in Determining Longevity 
260 |b MDPI AG,   |c 2023-04-01T00:00:00Z. 
500 |a 10.3390/antiox12040944 
500 |a 2076-3921 
520 |a Thioredoxin and thioredoxin reductase are evolutionarily conserved antioxidant enzymes that protect organisms from oxidative stress. These proteins also play roles in redox signaling and can act as a redox-independent cellular chaperone. In most organisms, there is a cytoplasmic and mitochondrial thioredoxin system. A number of studies have examined the role of thioredoxin and thioredoxin reductase in determining longevity. Disruption of either thioredoxin or thioredoxin reductase is sufficient to shorten lifespan in model organisms including yeast, worms, flies and mice, thereby indicating conservation across species. Similarly, increasing the expression of thioredoxin or thioredoxin reductase can extend longevity in multiple model organisms. In humans, there is an association between a specific genetic variant of thioredoxin reductase and lifespan. Overall, the cytoplasmic and mitochondrial thioredoxin systems are both important for longevity. 
546 |a EN 
690 |a aging 
690 |a lifespan 
690 |a thioredoxin 
690 |a reactive oxygen species 
690 |a redox signaling 
690 |a animal models 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 12, Iss 4, p 944 (2023) 
787 0 |n https://www.mdpi.com/2076-3921/12/4/944 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/0624c69f30cd461f81a75a962ce7a83d  |z Connect to this object online.