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PHA-induced cell proliferation rescues human peripheral blood lymphocytes from X-ray-induced apoptosis
Author(s) -
M. Carloni
Publication year - 2001
Publication title -
mutagenesis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.723
H-Index - 91
eISSN - 1464-3804
pISSN - 0267-8357
DOI - 10.1093/mutage/16.2.115
Subject(s) - dna laddering , apoptosis , programmed cell death , radioresistance , microbiology and biotechnology , biology , cell , cytotoxicity , dna damage , peripheral blood , dna fragmentation , lymphocyte , dna , immunology , chemistry , cell culture , biochemistry , genetics , in vitro
Human peripheral blood G(0) lymphocytes were X-irradiated and allowed to recover for different periods both in the presence and absence of phytohemagglutinin (PHA). For each experimental condition the induction of apoptosis was investigated by nuclear morphology and formation of both DNA laddering and high molecular weight DNA fragments by pulsed field gel electrophoresis. The results showed that PHA cell growth stimulation could rescue peripheral blood lymphocytes (PBLs) from X-ray-induced apoptotic cell death. Instead, most X-irradiated lymphocytes held in G(0) phase, once they were committed to apoptosis, inexorably executed the process. These data indicate that the proliferative status of PBLs can influence apoptotic cell death: PHA-stimulated PBLs appear to be more radioresistant as a result of a less efficient apoptotic process. Therefore, in current tests for mutagenicity or cytotoxicity and in biodosimetrical studies the possible role of apoptosis has to be considered.

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