| Literature DB >> 33022052 |
Ekaterina Royba1, Mikhail Repin1, Adayabalam S Balajee2, Igor Shuryak1, Sergey Pampou3, Charles Karan3, David J Brenner1, Guy Garty1.
Abstract
An automated platform for cytogenetic biodosimetry, the "Rapid Automated Biodosimetry Tool II (RABiT-II)," adapts the dicentric chromosome assay (DCA) for high-throughput mass-screening of the population after a large-scale radiological event. To validate this test, the U.S. Federal Drug Administration (FDA) recommends demonstrating that the high-throughput biodosimetric assay in question correctly reports the dose in an in vivo model. Here we describe the use of rhesus macaques (Macaca mulatta) to augment human studies and validate the accuracy of the high-throughput version of the DCA. To perform analysis, we developed the 17/22-mer peptide nucleic acid (PNA) probes that bind to the rhesus macaque's centromeres. To our knowledge, these are the first custom PNA probes with high specificity that can be used for chromosome analysis in M. mulatta. The accuracy of fully-automated chromosome analysis was improved by optimizing a low-temperature telomere PNA FISH staining in multiwell plates and adding the telomere detection feature to our custom chromosome detection software, FluorQuantDic V4. The dicentric frequencies estimated from in vitro irradiated rhesus macaque samples were compared to human blood samples of individuals subjected to the same ex vivo irradiation conditions. The results of the RABiT-II DCA analysis suggest that, in the lymphocyte system, the dose responses to gamma radiation in the rhesus macaques were similar to those in humans, with small but statistically significant differences between these two model systems. ©2020 by Radiation Research Society. All rights of reproduction in any form reserved.Entities:
Mesh:
Year: 2020 PMID: 33022052 PMCID: PMC9039759 DOI: 10.1667/RR15547.1
Source DB: PubMed Journal: Radiat Res ISSN: 0033-7587 Impact factor: 3.372