Human promyelocytic leukemia HL-60 cells have been used as a model to study
both the expression of matrix-metalloproteinases and the mechanisms of pro
grammed cell death. In the present study we examined the expression of thes
e proteases in HL-60 cells stimulated by different apoptotic triggers. As s
hown by zymography, HL-60 cells released three major isofroms of the matrix
-degrading proteases; when the leukemic cells were grown in serum-free cond
itions, as well as after hyperthermia and methotrexate treatment, we found
a significant loss of the constitutive production of the 92 kDa matrix-meta
lloprotease, with an unequivocable molecular and ultrastructural evidence o
f programmed cell death. These results suggest that in HL-60 cells the expr
ession/release of matrix metalloproteases can be down-regulated in the pres
ence of the apoptotic-induced alterations, and that the decreased matrix-de
grading capacity of this leukemic cell line during apoptosis may reduce its
invasive potential.