M. Jeziorska et al., IMMUNOLOCALIZATION OF THE MATRIX METALLOPROTEINASES GELATINASE-B AND STROMELYSIN-I IN HUMAN ENDOMETRIUM THROUGHOUT THE MENSTRUAL-CYCLE, Journal of Reproduction and Fertility, 107(1), 1996, pp. 43-51
Immunolocalization techniques were used to examine the distribution of
the matrix metalloproteinases gelatinase B and stromelysin 1 in human
endometrial specimens, taken across the normal menstrual cycle. Gelat
inase B was produced by glandular epithelial cells for approximately 7
days during the proliferative phase, with polymorphonuclear leucocyte
s, macrophages and eosinophils providing most of this enzyme at menstr
uation. There was no evidence that gelatinase B is produced by stromal
cells or mast cells during the cycle. Immunoreactive gelatinase B in
glandular epithelial cells was greatest during the late proliferative
phase and just after ovulation; its presence in glandular secretion an
d the uterine fluid was optimal during the peri-implantation phase. Ge
latinase B was clearly associated with an influx of polymorphonuclear
leucocytes, macrophages and eosinophils just before, and during, menst
ruation. In contrast, immunostaining for stromelysin 1 was much weaker
than that for gelatinase B, and was present only around stromal cells
and limited to microfocal locations at times coincident with stromal
oedema (days 8-10 and 21-22). Both enzymes were widely distributed in
specimens just before and during menstruation, and were particularly p
rominent in connective tissue stroma and vascular basement membranes.
Specimens at the early proliferative stage were devoid of both enzymes
. The data provide further evidence supporting a role for metalloprote
inases in endometrial biology, not only in matrix remodelling during t
he cycle, but also in glandular secretions potentially relevant to bla
stocyst recognition and implantation. Our observations emphasize the f
unctional importance of specific cell types and the temporal regulatio
n of gelatinase B and stromelysin 1 throughout the normal menstrual cy
cle.