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mBAND Analysis of Late Chromosome Aberrations in Human Lymphocytes Induced by Gamma Rays and Fe IonsChromosomal translocations and inversions are considered stable, and cells containing these types of chromosome aberrations can survive multiple cell divisions. An efficient method to detect an inversion is multi-color banding fluorescent in situ hybridization (mBAND) which allows identification of both inter- and intrachromosome aberrations simultaneously. Post irradiation, chromosome aberrations may also arise after multiple cell divisions as a result of genomic instability. To investigate the stable or late-arising chromosome aberrations induced after radiation exposure, we exposed human lymphocytes to gamma rays and Fe ions ex vivo, and cultured the cells for multiple generations. Chromosome aberrations were analyzed in cells collected at first mitosis and at several time intervals during the culture period post irradiation. With gamma irradiation, about half of the damages observed at first mitosis remained after 7 day- and 14 day- culture, suggesting the transmissibility of damages to the surviving progeny. Detailed analysis of chromosome break ends participating in exchanges revealed a greater fraction of break ends involved in intrachromosome aberrations in the 7- and 14-day samples in comparison to the fraction at first mitosis. In particular, simple inversions were found at 7 and 14 days, but not at the first mitosis, suggesting that some of the aberrations might be formed days post irradiation. In contrast, at the doses that produced similar frequencies of gamma-induced chromosome aberrations as observed at first mitosis, a significantly lower yield of aberrations remained at the same population doublings after Fe ion exposure. At these equitoxic doses, more complex type aberrations were observed for Fe ions, indicating that Fe ion-induced initial chromosome damages are more severe and may lead to cell death. Comparison between low and high doses of Fe ion irradiation in the induction of late damages will also be discussed.
Document ID
20140012618
Acquisition Source
Johnson Space Center
Document Type
Presentation
Authors
Sunagawa, Mayumi
(Texas Southern Univ. Houston, TX, United States)
Zhang, Ye
(Wyle Labs., Inc. Houston, TX, United States)
Yeshitla, Samrawit
(Texas Southern Univ. Houston, TX, United States)
Kadhim, Munira
(Oxford Brookes Univ. Headington, United Kingdom)
Wilson, Bobby
(Texas Southern Univ. Houston, TX, United States)
Wu, Honglu
(NASA Johnson Space Center Houston, TX, United States)
Date Acquired
September 26, 2014
Publication Date
February 12, 2014
Subject Category
Life Sciences (General)
Aerospace Medicine
Report/Patent Number
JSC-CN-30551
Meeting Information
Meeting: NASA Human Research Program Investigators Workshop (HRP 2014)
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., NASA Headquarters
Distribution Limits
Public
Copyright
Public Use Permitted.
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