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Visit our Expo - Redox and Inflammation signaling 2012

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Session X : Cell death in cancer Poster X, 72<br />

Oxidative stress response in telomerized human fibroblasts from a centenarian<br />

Chiara Mondello1, Maria Grazia Bottone1,2, Sakon Noriki3, Cristiana Soldani2, Carlo<br />

Pellicciari2, A. Ivana Scovassi1<br />

1 Istituto di Genetica Molecolare del CNR, Via Abbiategrasso 207, 27100 Pavia, Italy, Email:<br />

mondello@igm.cnr.it, scovassi@igm.cnr.it; 2 Dipartimento di Biologia Animale,<br />

Piazza Botta 10, 27100, Pavia, Italy. E-mail: bottone@unipv.it, soldani@unipv.it,<br />

pelli@unipv.it; 3 Department of Oncological Pathology, Faculty of Medicine, Matsuoka,<br />

Yoshida-Gun, 9l0-ll93, Fukui, Japan. E-mail: noriki@fmsrsa.fukui-med.ac.jp<br />

It has been reported that cells with ectopic expression of telomerase (so-called telomerized)<br />

are more resistant to apoptotic cell death than their normal counterpart. However,<br />

controversial results have been obtained as to the response of telomerized cells to the<br />

oxidative stress. In the present research, we investigated the effects of the treatment with<br />

either tert-butylhydroperoxide (tBOOH) or 2-deoxy-D-ribose (D-ribose) on human fibroblasts<br />

from a centenarian individual (cen3) <strong>and</strong> on their counterpart with reactivated telomerase<br />

(cen3tel). Our results suggest that the effects of these drugs are modulated by telomerase<br />

reactivation. In fact, after drug treatment the cell number of both cell lines was lower than in<br />

controls, indicating that both agents impaired cell proliferation; remarkably, proliferation was<br />

always inhibited at a larger extent in cen3tel than in cen3 cells. Different parameters of<br />

apoptosis were also studied in situ (i.e., chromatin condensation, phosphatidylserine<br />

externalization, <strong>and</strong> DNA fragmentation) <strong>and</strong> showed that the percentage of apoptotic cells<br />

was lower in telomerized cell cultures, although apoptosis could not completely account for<br />

the observed cell loss in treated cultures. The evidence of active phagocytosis of apoptotic<br />

cells occurring in <strong>our</strong> fibroblast cultures provides an explanation for these contradictory<br />

results.<br />

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