This study shows that human postthymic T cells express CD10 when undergoing
apoptosis, irrespective of the signal responsible for initiating the apopt
otic process. Cells from continuous T-cell lines did not normally express C
D10, but became CD10(+) when induced into apoptosis by human immunodeficien
cy virus (HIV) infection and exposure to CD95 monoclonal antibody, etoposid
e, or staurosporin. Inhibitors of caspases blocked apoptosis and CD10 expre
ssion. Both CD4(+) and CD8(+) T cells purified from normal peripheral blood
expressed CD10 on apoptotic induction. CD10 was newly synthesized by the a
poptosing cells because its expression was inhibited by exposure to cyclohe
ximide 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 su
bstantial, although variable, proportion of apoptosing T cells that consist
ently expressed CD10. In contrast, CD10(+) as well as spontaneously apoptos
ing T cells were virtually absent in peripheral blood from normal individua
ls. Collectively, these observations indicate that CD10 may represent a rel
iable marker for identifying and isolating apoptosing T cells in vitro and
ex vivo and possibly suggest novel functions for surface CD10 in the apopto
tic process of lymphoid cells. (C) 1999 by The American Society of Hematolo
gy.