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Suppressed PHA activation of T lymphocytes in simulated microgravity is restored by direct activation of protein kinase CUtilizing clinostatic rotating wall vessel (RWV) bioreactors that simulate aspects of microgravity, we found phytohemagglutinin (PHA) responsiveness to be almost completely diminished. Activation marker expression was significantly reduced in RWV cultures. Furthermore, cytokine secretion profiles suggested that monocytes are not as adversely affected by simulated microgravity as T cells. Reduced cell-cell and cell-substratum interactions may play a role in the loss of PHA responsiveness because placing peripheral blood mononuclear cells (PBMC) within small collagen beads did partially restore PHA responsiveness. However, activation of purified T cells with cross-linked CD2/CD28 and CD3/CD28 antibody pairs was completely suppressed in the RWV, suggesting a defect in signal transduction. Activation of purified T cells with PMA and ionomycin was unaffected by RWV culture. Furthermore, sub-mitogenic doses of PMA alone but not ionomycin alone restored PHA responsiveness of PBMC in RWV culture. Thus our data indicate that during polyclonal activation the signaling pathways upstream of PKC activation are sensitive to simulated microgravity.
Document ID
20040172701
Acquisition Source
Legacy CDMS
Document Type
Reprint (Version printed in journal)
Authors
Cooper, D.
(Graduate School of Biomedical Sciences, The University of Texas Health Science Center at Houston United States)
Pellis, N. R.
McIntire, L. V.
Date Acquired
August 22, 2013
Publication Date
May 1, 1998
Publication Information
Publication: Journal of leukocyte biology
Volume: 63
Issue: 5
ISSN: 0741-5400
Subject Category
Life Sciences (General)
Report/Patent Number
ISSN: 0741-5400
Distribution Limits
Public
Copyright
Other
Keywords
NASA Discipline Cell Biology
Non-NASA Center
Protein Kinase C/physiology
T-Lymphocytes/immunology
Weightlessness
Lymphocyte Activation
Cells, Cultured
Support, U.S. Gov't, Non-P.H.S
Cell Division
Cell Adhesion
Models, Biological
Ionomycin/pharmacology
Support, Non-U.S. Gov't
Enzyme Activation
Antigen-Antibody Reactions
Immunophenotyping
Interleukin-2/pharmacology
Cytokines/secretion
Signal Transduction
Human
Bioreactors

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