Maximizing Science Return from Future Rodent Experiments on the International Space Station (ISS): Tissue PreservationTo better understand how mammals adapt to long duration habitation in space, a system for performing rodent experiments on the ISS is under development; Rodent Research-1 is the first flight and will include validation of both on-orbit animal support and tissue preservation. To evaluate plans for on-orbit sample dissection and preservation, we simulated conditions for euthanasia, tissue dissection, and prolonged sample storage on the ISS, and we also developed methods for post-flight dissection and recovery of high quality RNA from multiple tissues following prolonged storage in situ for future science. Mouse livers and spleens were harvested under conditions that simulated nominal, on-orbit euthanasia and dissection operations including storage at -80 C for 4 months. The RNA recovered was of high quality (RNA Integrity Number, RIN(is) greater than 8) and quantity, and the liver enzyme contents and activities (catalase, glutathione reductase, GAPDH) were similar to positive controls, which were collected under standard laboratory conditions. We also assessed the impact of possible delayed on-orbit dissection scenarios (off-nominal) by dissecting and preserving the spleen (RNAlater) and liver (fast-freezing) at various time points post-euthanasia (from 5 min up to 105 min). The RNA recovered was of high quality (spleen, RIN (is) greater than 8; liver, RIN (is) greater than 6) and liver enzyme activities were similar to positive controls at all time points, although an apparent decline in select enzyme activities was evident at the latest time (105 min). Additionally, various tissues were harvested from either intact or partially dissected, frozen carcasses after storage for approximately 2 months; most of the tissues (brain, heart, kidney, eye, adrenal glands and muscle) were of acceptable RNA quality for science return, whereas some tissues (small intestine, bone marrow and bones) were not. These data demonstrate: 1) The protocols developed for future flight experiments will support science return despite delayed preservation post-euthanasia or prolonged storage, and 2) Many additional tissues for gene expression analysis can be obtained by dissection following prolonged storage of the tissue in situ at -80 C. These findings have relevance both to high value, ground-based experiments when sample collection capability is severely constrained, and to all future spaceflight experiments that entail on-orbit sample recovery by the ISS crew.
Document ID
20150000115
Acquisition Source
Ames Research Center
Document Type
Abstract
Authors
Choi, S. Y. (Lockheed Martin Space Operations Moffett Field, CA, United States)
Lai, S. (Lockheed Martin Space Operations Moffett Field, CA, United States)
Klotz, R. (Lockheed Martin Space Operations Moffett Field, CA, United States)
Popova, Y. (Oak Ridge Associated Universities Moffett Field, CA, United States)
Chakravarty, K. (Lockheed Martin Space Operations Moffett Field, CA, United States)
Beegle, J. E. (NASA Ames Research Center Moffett Field, CA, United States)
Wigley, C. L. (NASA Ames Research Center Moffett Field, CA, United States)
Globus, R. K. (NASA Ames Research Center Moffett Field, CA, United States)
Date Acquired
January 5, 2015
Publication Date
October 23, 2014
Subject Category
Space Sciences (General)
Report/Patent Number
ARC-E-DAA-TN15995Report Number: ARC-E-DAA-TN15995
Meeting Information
Meeting: American Society for Gravitational and Space Biology (ASGSR)
Location: Pasadena, CA
Country: United States
Start Date: October 23, 2014
End Date: October 26, 2014
Sponsors: American Society for Gravitational and Space Biology
IDRelationTitle20160003293See AlsoMaximizing Science Return from Future Rodent Experiments on the International Space Station (ISS): Tissue Preservation20160003293See AlsoMaximizing Science Return from Future Rodent Experiments on the International Space Station (ISS): Tissue Preservation