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Blood, Vol. 94 No. 9 (November 1), 1999: pp. 3067-3076

Expression of CD10 by Human T Cells That Undergo Apoptosis Both In Vitro and In Vivo

Giovanna Cutrona, Nicolò Leanza, Massimo Ulivi, Giovanni Melioli, Vito L. Burgio, Giovanni Mazzarello, Giovanni Gabutti, Silvio Roncella, and Manlio Ferrarini

From the Servizio di Immunologia Clinica and Servizio di Citometria CBA, Istituto Nazionale per la Ricerca sul Cancro, IST---Genoa; the a Fondazione Andrea Cesalpino, Istituto di 1 Clinica Medica, Università "La Sapienza," Rome; the Ia  Clinica Malattie Infettive, and the Istituto di Igiene, Università di Genova, Genoa; the Servizio di Istologia e Anatomia Patologica, Ospedale Sant'Andrea, La Spezia; and the Dipartimento di Oncologia, Biologia e Genetica, Università di Genova, Genoa, Italy.

This study shows that human postthymic T cells express CD10 when undergoing apoptosis, irrespective of the signal responsible for initiating the apoptotic process. Cells from continuous T-cell lines did not normally express CD10, but became CD10+ when induced into apoptosis by human immunodeficiency virus (HIV) infection and exposure to CD95 monoclonal antibody, etoposide, or staurosporin. Inhibitors of caspases blocked apoptosis and CD10 expression. Both CD4+ and CD8+ T cells purified from normal peripheral blood expressed CD10 on apoptotic induction. CD10 was newly synthesized by the apoptosing cells because its expression was inhibited by exposure to cycloheximide and CD10 mRNA became detectable by reverse transcription-polymerase chain reaction in T cells cultured under conditions favoring apoptosis. To show CD10 on T cells apoptosing in vivo, lymph node and peripheral blood T cells from HIV+ subjects were used. These suspensions were composed of a substantial, although variable, proportion of apoptosing T cells that consistently expressed CD10. In contrast, CD10+ as well as spontaneously apoptosing T cells were virtually absent in peripheral blood from normal individuals. Collectively, these observations indicate that CD10 may represent a reliable marker for identifying and isolating apoptosing T cells in vitro and ex vivo and possibly suggest novel functions for surface CD10 in the apoptotic process of lymphoid cells.


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