L-selectin, a surface adhesion glycoprotein expressed on leukocytes, has a
well-established role in mediating inflammation and lymphocyte recirculatio
n. Recent evidence suggests that L-selectin may also influence hematopoiesi
s. We observed that a greater proportion of CD34+ cells express L-selectin
in cord blood compared with adult bone marrow, and we hypothesized that L-s
electin expression is associated with enhanced clonogenic properties. To te
st this, we compared CD34+/L-selectin+ cells with CD34+/L-selectin- cells i
n hematopoietic clonogenic assays, From CD34+/L-selectin+ cell cultures, we
observed a 3-fold increase of d 12-14 colony-forming unit-granulocyte/macr
ophage and multipotent progenitor cells, and a 5-fold enhancement of primit
ive d 21 high proliferative potential colony-forming cells compared with th
e progeny of CD34+/L-selectin- cells. We conclude that CD34+ cord blood cel
ls expressing L-selectin are enriched in their clonogenic activity compared
with cell fractions lacking L-selectin expression.