Haemopoietic progenitor cells (HPCs) express the CD34 molecule, a heavily g
lycosylated transmembrane protein displaying three main classes of epitopes
. The CD34 epitope class expression may vary between different subsets of H
PCs. The aim of this study was to characterise the subsets of HPCs expressi
ng CD34 class II and III epitopes. The cells were studied for coexpression
of activation-, lineage- and adhesion-associated molecules, and their clono
genic ability and morphological features were examined.
CD34(+) HPCs expressing class III epitopes outnumbered those expressing cla
ss II. Class III expressing HPCs were enriched for CFU-GM and BFU-E and cel
ls coexpressing CD13, CD33, c-kit and CD71 compared to class II expressing
HPCs. CD34(+) cells exclusively expressing class III epitopes uniformly dis
played CD13 and CD33; they had a high clonogenic capacity and morphological
characteristics of promyelocytes and myelocytes.
The data show that class III epitopes are distributed more broadly on CD34(
+) HPCs than are class II epitopes, and that lack of class II epitopes is c
onfined to CD34(+) HPCs at a late stage of myeloid differentiation. The hig
her number of class III expressing HPCs coexpressing c-kit and CD71 suggest
s that these cells exhibit a higher proliferative or differential potential
than do HPCs expressing class II epitopes.