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   <subfield code="a">Chromosome aberration measurements in mitotic and G2-PCC lymphocytes at the standard sampling time of 48h underestimate the effectiveness of high-LET particles</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ryonfa Lee, Elena Nasonova, Carola Hartel, Marco Durante, Sylvia Ritter]</subfield>
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   <subfield code="a">The relationship between heavy-ion-induced cell cycle delay and the time-course of aberrations in first-cycle metaphases or prematurely condensed G2-cells (G2-PCC) was investigated. Lymphocytes of the same donor were irradiated with X-rays or various charged particles (carbon, iron, xenon, and chromium) covering an LET range of 2-3,160keV/μm. Chromosome aberrations were measured in samples collected at 48, 60, 72, and 84h postirradiation. Linear-quadratic functions were fitted to the data, and the fit parameters α and β were determined. At any sampling time, α values derived from G2-cells were higher than those from metaphases. The α value derived from metaphase analysis at 48h increased with LET, reached a maximum around 155keV/μm, and decreased with a further rise in LET. At the later time-points, higher α values were estimated for particles with LET&gt;30keV/μm. Estimates of α values from G2-cells showed a similar LET dependence, yet the time-dependent increase was less pronounced. Altogether, our data demonstrate that heavily damaged lymphocytes suffer a prolonged G2-arrest that is clearly LET dependent. For this very reason, the standard analysis of aberrations in metaphase cells 48h postirradiation will considerably underestimate the effectiveness of high-LET radiation. Scoring of aberrations in G2-PCC at 48h as suggested by several authors will result in higher aberration yields. However, when particles with a very high-LET value (LET&gt;150keV/μm) are applied, still a fraction of multiple damaged cells escape detection by G2-analysis 48h postirradiation.</subfield>
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