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Overview | Description | Applications | Operations | Results | Publications | Images
Experiment/Payload OverviewWhite blood cells (lymphocytes) are collected from crewmembers preflight and postflight. The lymphocytes are examined using different analytic methods to determine quantity and quality of genetic changes resulting from exposure to cosmic radiation, particularly ionizing radiation.
Principal InvestigatorJohnson Space Center, Human Research Program, Houston, TX
Sponsoring AgencyNational Aeronautics and Space Administration (NASA)
Expeditions Assigned|6|7|8|9|10|11|13|
Previous ISS MissionsAn earlier version of this experiment flew on the Space Shuttle and the Russian Space Station Mir. This investigation has been performed on ISS Expeditions 6-11.
Crewmembers are exposed to radiation when they leave the protection of Earth's atmosphere. Ionizing radiation in particular can damage chromosomes, causing mutations such as chromosome aberrations. To assess the genetic impact of this radiation, blood is drawn before and immediately after flight by venous puncture. The blood is then cultured and the lymphocytes are stimulated to undergo mitosis (the process of cell division). In the first mitosis, at about 48 hours of incubation, the process is stopped and the chromosomes are prepared and stained using three different methods of microscopic analysis to assess all types of aberrations induced by ionizing radiations. These methods are:
From this study scientists may be able to better assess risk factors for genetic damage in space and help develop new methods for protecting crewmembers. Understanding and reducing the risk of radiation is important for safe long duration travel in space, including stays on the Moon and travel to Mars.
Earth ApplicationsThe knowledge gained from this investigation will give scientist's insight into the exact chromosome from which particular mutations arise.
Chromosome does not have any inflight requirements. Samples will be taken before and after flight.
Operational ProtocolsThe researchers will take venous blood samples (10 to 15 ml from the crew participants shortly before and after flight.
In each Expedition where the experiment has been conducted, preflight and postflight blood samples were drawn from each crewmember. To ensure high-quality results, the blood samples arrive at the laboratory within 72 hours after collection. Researchers are currently measuring changes in the genetic material and analyzing their significance and will release preliminary conclusions soon. From this study scientists may be able to better assess risk factors for genetic damage in space. Understanding and reducing the risk of radiation is important for safe long-duration travel in space, including stays on the moon and journeys to Mars.
Giemsa stained metaphase with a chromatid break (one of the arms of the chromosome broke off). Image on the right is a detailed of the chromatid break. It is also visible in the image on the left, in the lower right corner of the picture. Image courtesy of NASA.
Giemsa stained metaphase with several aberrations, i.e. polycentric chromosomes and acentric fragments. Polycentric chromosomes are attached to each other multiple times (unaltered chromosomes have one center). Acentric fragments have no attachment to the rest of the chromosome they originate from. Image courtesy of NASA.
Researchers use mFISH to study human chromosomal pairs. Multi-color fluorescence in situ hybridization (mFISH) metaphase with an interstitial deletion of chromosome 1. The Chromosome 1 pair are the long yellow chromosomes located in the right center of the (that is the chromosome with the deletion) and on the left outer center of the picture. Image courtesy of University of Duisburg-Essen.
Researchers use mFISH to study human chromosomal pairs. Multi-color fluorescence in situ hybridization (mFISH) metaphase with an interstitial deletion of chromosome 1. Chromosomes organized according to their pair number. Image courtesy of University of Duisburg-Essen.
Multi-color fluorescence in situ hybridization (mFISH) metaphase with a reciprocal translocation between chromosomes 3 and 7. Image courtesy of University of Duisburg-Essen.
Multi-color fluorescence in situ hybridization (mFISH) metaphase with a reciprocal translocation between chromosomes 3 and 7. Chromosomes organized according to their pair number. Image courtesy of University of Duisburg-Essen.
Multi-color banding fluorescence in situ hybridization (mBAND) is done on Chromosome 5 only. This image depicts a chromosome 5 with an interstitial deletion (part of the chromosome is detached). Image courtesy of University of Duisburg-Essen.
Multi-color fluorescence in situ hybridization (mFISH) metaphase with a complex translocation pattern. Translocations are present between chromosome 3 and the X-chromosome; chromosomes 7 and 21, and chromosomes 7, 12 and 15.Image courtesy of University of Duisburg-Essen.
Multi-color fluorescence in situ hybridization (mFISH) metaphase with a reciprocal translocation between chromosomes 9 and 11 (encircled). Image courtesy of University of Duisburg-Essen.