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Three-Dimensional Normal Human Neutral Progenitor Tissue-Like Assemblies: A Model for Persistent Varicella-Zoster Virus Infection and Platform to Study Oxidate Stress and Damage in Multiple Hit ScenariosThe environment of space results in a multitude of challenges to the human physiology that present barriers to extended habitation and exploration. Over 40 years of investigation to define countermeasures to address space flight adaptation has left gaps in our knowledge regarding mitigation strategies partly due to the lack of investigative tools, monitoring strategies, and real time diagnostics to understand the central causative agent(s) responsible for physiologic adaptation and maintaining homeostasis. Spaceflight-adaptation syndrome is the combination of space environmental conditions and the synergistic reaction of the human physiology. Our work addresses the role of oxidative stress and damage (OSaD) as a negative and contributing Risk Factor (RF) in the following areas of combined spaceflight related dysregulation: i) radiation induced cellular damage [1], [2] ii) immune impacts and the inflammatory response [3], [4] and iii) varicella zoster virus (VZV) reactivation [5]. Varicella-zoster (VZV)/Chicken Pox virus is a neurotropic human alphaherpes virus resulting in varicella upon primary infection, suppressed by the immune system becomes latent in ganglionic neurons, and reactivates under stress events to re-express in zoster and possibly shingles. Our laboratory has developed a complex three-dimensional (3D) normal human neural tissue model that emulates several characteristics of the human trigeminal ganglia (TG) and allows the study of combinatorial experimentation which addresses, simultaneously, OSaD associated with Spaceflight adaptation and habitation [6]. By combining the RFs of microgravity, radiation, and viral infection we will demonstrate that living in the space environment leads to significant physiological consequences for the peripheral and subsequently the central nervous system (PNS, CNS) associated with OSaD generation and consequentially endangers long-duration and exploration-class missions.
Document ID
20140003856
Acquisition Source
Johnson Space Center
Document Type
Conference Paper
Authors
Goodwin, Thomas J.
(NASA Johnson Space Center Houston, TX, United States)
McCarthy, M.
(Texas Univ. Medical Branch Galveston, TX, United States)
Osterrieder, N.
(Freie Univ. Berlin, Germany)
Cohrs, R. J.
(Colorado Univ. Aurora, CO, United States)
Kaufer, B. B.
(Freie Univ. Berlin, Germany)
Date Acquired
April 28, 2014
Publication Date
February 12, 2014
Subject Category
Aerospace Medicine
Report/Patent Number
JSC-CN-30045
Report Number: JSC-CN-30045
Meeting Information
Meeting: NASA Human Research Program Investigators'' Workshop
Location: Galveston, TX
Country: United States
Start Date: February 12, 2014
End Date: February 13, 2014
Sponsors: Universities Space Research Association, National Space Biomedical Research Inst.
Distribution Limits
Public
Copyright
Public Use Permitted.
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