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Changes in expression of genes involved in apoptosis in activated human T-cells in response to modeled microgravity
Authors:Nancy E Ward  Neal R Pellis  Diana Risin MD  PhD  Semyon A Risin  Wenbin Liu
Affiliation:1. Wyle Laboratories, Life Sciences Group, Italy
2. Human Adaptation and Countermeasures Office (HACO), NASA Johnson Space Center, 2101 NASA Parkway Mail code: SK, 77058-3696, Houston, TX
3. Department of Pathology and Laboratory Medicine, University of Texas-Houston Medical School, Italy
4. Microarray Core Facility and Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, U.S.A
Abstract:Space flights result in remarkable effects on various physiological systems, including a decline in cellular immune functions. Previous studies have shown that exposure to microgravity, both true and modeled, can cause significant changes in numerous lymphocyte functions. The purpose of this study was to search for microgravity-sensitive genes, and specifically for apoptotic genes influenced by the microgravity environment and other genes related to immune response. The experiments were performed on anti-CD3 and IL-2 activated human T cells. To model microgravity conditions we have utilized the NASA rotating wall vessel bioreactor. Control lymphocytes were cultured in static 1g conditions. To assess gene expression we used DNA microarray chip technology. We had shown that multiple genes (approximately 3–8% of tested genes) respond to microgravity conditions by 1.5 and more fold change in expression. There is a significant variability in the response. However, a certain reproducible pattern in gene response could be identified. Among the genes showing reproducible changes in expression in modeled microgravity, several genes involved in apoptosis as well as in immune response were identified. These are IL-7 receptor, Granzyme B, Beta-3-endonexin, Apo2 ligand and STAT1. Possible functional consequences of these changes are discussed.
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