M. Bauchinger et al., Collaborative exercise on the use of FISH chromosome painting for retrospective biodosimetry of Mayak nuclear-industrial personnel, INT J RAD B, 77(3), 2001, pp. 259-267
Purpose: To investigate within the framework of a multilaboratory study the
suitability of FISH chromosome painting to measure so-called stable transl
ocations in peripheral lymphocytes of Mayak nuclear-industrial workers (fro
m the Southern Urals) and their use for retrospective biodosimetry.
Material and methods: Chromosome analyses were carried out from 69 workers
who had received protracted occupational radiation exposures (0.012-6.065 G
y) up to similar to 40 years before blood sampling. Twenty-one unexposed pe
ople living in the same area were controls. A multicolour FISH-painting pro
tocol with the target chromosomes 1, 4 and 8 simultaneously with a pancentr
omeric probe was used to score potentially transmissible chromosome-type ab
errations (reciprocal translocations 2B and related 'one-way' patterns I-II
I according to the S&S classification).
Results: Individual biodosimetry estimates were obtained in terms of these
potentially long-term surviving aberration types based on the linear compon
ent of a low dose-rate gamma -ray calibration curve produced using identica
l staining and scoring protocols. For comparison, the workers' personal and
total background doses were converted to red bone marrow doses. The estima
ted doses were mainly lower than would be predicted by the calibration curv
e, particularly at accumulated higher dose levers.
Conclusions: Owing to the limited life-time of circulating T-lymphocytes, t
he long-term persistence of translocations in vivo requires the assumption
of a clonal repopulation of these naturally senescing cells from the haemop
oietic stem cell compartments. Obviously such a replacement cannot be fully
achieved, leading to a temporal decline even of the yield of transmissible
aberrations types. Assuming further a highly selective capacity of stem ce
lls against any type of chromosomal damage and the fact that one must rely
on partial genome findings, the potential of FISH chromosome painting for r
etrospective dose reconstruction is probably limited to a decade or so afte
r high-level protracted radiation exposure.