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Use of an adaptable cell culture kit for performing lymphocyte and monocyte cell cultures in microgravityThe results of experiments performed in recent years on board facilities such as the Space Shuttle/Spacelab have demonstrated that many cell systems, ranging from simple bacteria to mammalian cells, are sensitive to the microgravity environment, suggesting gravity affects fundamental cellular processes. However, performing well-controlled experiments aboard spacecraft offers unique challenges to the cell biologist. Although systems such as the European 'Biorack' provide generic experiment facilities including an incubator, on-board 1-g reference centrifuge, and contained area for manipulations, the experimenter must still establish a system for performing cell culture experiments that is compatible with the constraints of spaceflight. Two different cell culture kits developed by the French Space Agency, CNES, were recently used to perform a series of experiments during four flights of the 'Biorack' facility aboard the Space Shuttle. The first unit, Generic Cell Activation Kit 1 (GCAK-1), contains six separate culture units per cassette, each consisting of a culture chamber, activator chamber, filtration system (permitting separation of cells from supernatant in-flight), injection port, and supernatant collection chamber. The second unit (GCAK-2) also contains six separate culture units, including a culture, activator, and fixation chambers. Both hardware units permit relatively complex cell culture manipulations without extensive use of spacecraft resources (crew time, volume, mass, power), or the need for excessive safety measures. Possible operations include stimulation of cultures with activators, separation of cells from supernatant, fixation/lysis, manipulation of radiolabelled reagents, and medium exchange. Investigations performed aboard the Space Shuttle in six different experiments used Jurkat, purified T-cells or U937 cells, the results of which are reported separately. We report here the behaviour of Jurkat and U937 cells in the GCAK hardware in ground-based investigations simulating the conditions expected in the flight experiment. Several parameters including cell concentration, time between cell loading and activation, and storage temperature on cell survival were examined to characterise cell response and optimise the experiments to be flown aboard the Space Shuttle. Results indicate that the objectives of the experiments could be met with delays up to 5 days between cell loading into the hardware and initial in flight experiment activation, without the need for medium exchange. Experiment hardware of this kind, which is adaptable to a wide range of cell types and can be easily interfaced to different spacecraft facilities, offers the possibility for a wide range of experimenters successfully and easily to utilise future flight opportunities.
Document ID
20040172624
Acquisition Source
Legacy CDMS
Document Type
Reprint (Version printed in journal)
Authors
Hatton, J. P.
(INSERM U311, Etablissement de Transfusion Sanguine, Strasbourg, France)
Lewis, M. L.
Roquefeuil, S. B.
Chaput, D.
Cazenave, J. P.
Schmitt, D. A.
Date Acquired
August 22, 2013
Publication Date
August 1, 1998
Publication Information
Publication: Journal of cellular biochemistry
Volume: 70
Issue: 2
ISSN: 0730-2312
Subject Category
Life Sciences (General)
Report/Patent Number
ISSN: 0730-2312
Distribution Limits
Public
Copyright
Other
Keywords
short duration
manned
Flight Experiment
Non-NASA Center
STS Shuttle Project
NASA Discipline Cell Biology
Cell Culture/instrumentation/methods
Lymphocytes
Weightlessness
Monocytes
Tumor Cells, Cultured
Cold
Jurkat Cells
Space Flight
Human
Phorbol Esters/pharmacology
Support, U.S. Gov't, Non-P.H.S
Temperature
Protein Kinase C/metabolism
Cell Size
Culture Media
Support, Non-U.S. Gov't
Cytokines/biosynthesis
Cell Survival
Biological Transport

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