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Role of Mitochondrial Oxidative Stress in Spaceflight-Induced Tissue DegenerationMicrogravity and ionizing radiation in the spaceflight environment poses multiple challenges to homeostasis and may contribute to cellular stress. Effects may include increased generation of reactive oxygen species (ROS), DNA damage and repair error, cell cycle arrest, cell senescence or death. Our central hypothesis is that prolonged exposure to the spaceflight environment leads to the excess production of ROS and oxidative damage, culminating in accelerated tissue degeneration. The main goal of this project is to determine the importance of cellular redox defense for physiological adaptations and tissue degeneration in the space environment.
Document ID
20180000859
Acquisition Source
Ames Research Center
Document Type
Presentation
Authors
Torres, Samantha M.
(Blue Marble Space Seattle, WA, United States)
Schreurs, Ann-Sofie
(Universities Space Research Association Moffett Field, CA, United States)
Truong, Tiffany A.
(Wyle Labs., Inc. Moffett Field, CA, United States)
Tahimic, Candice
(Wyle Labs., Inc. Moffett Field, CA, United States)
Globus, Ruth
(NASA Ames Research Center Moffett Field, CA, United States)
Date Acquired
January 31, 2018
Publication Date
October 25, 2017
Subject Category
Aerospace Medicine
Life Sciences (General)
Report/Patent Number
ARC-E-DAA-TN48022
Report Number: ARC-E-DAA-TN48022
Meeting Information
Meeting: Annual Meeting, American Society for Gravitational and Space Research (ASGSR 2017)
Location: Seattle, WA
Country: United States
Start Date: October 25, 2017
End Date: October 28, 2017
Sponsors: American Society for Gravitational and Space Research
Funding Number(s)
CONTRACT_GRANT: NNA14AB82C
CONTRACT_GRANT: NNX15AG98A
CONTRACT_GRANT: NNA16BD14C
Distribution Limits
Public
Copyright
Use by or on behalf of the US Gov. Permitted.
Keywords
transgenic mic
reactive oxygen species
spaceflight
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