N. Chegini et al., Expression of matrix metalloproteinase (MMP-1) and tissue inhibitor of MMPin serosal tissue of intraperitoneal organs and adhesions, FERT STERIL, 76(6), 2001, pp. 1212-1219
Objective: To compare expression of matrix metalloproteinase (MMP-1) and ti
ssue inhibitor of MMP (MMP-1) in serosal tissue of intraperitoneal organs a
nd adhesions.
Design: Prospective and cross-sectional study.
Setting: Academic research centers.
Patient(s): Patients undergoing abdominal or pelvic surgery.
Intervention(s): MMP-1 and TIMP-1 expression.
Main Outcome Measure(s): Expression of messenger ribonucleic acid (mRNA) an
d protein was measured by using quantitative reverse transcription polymera
se chain reaction (RT-PCR) and enzyme-linked immunosorbent assay.
Result(s): Serosal tissue of intraperitoneal organs and adhesions express M
MP-1 and TIMP-1 mRNA and protein at levels that are consistently varied wit
h 10- to 10.000-fold and 2- to 10-fold higher TIMP, rnRNA and protein, resp
ectively. Parietal peritoneum, fallopian tubes and ovaries express higher M
MP-1 mRNA levels compared with uterus and adhesions; the lowest expression
is found in small and large bowels, subcutaneous tissue. and omentum. Expre
ssion of TIMP-1 mRNA was less variable; the highest level was found in the
uterus and the lowest in subcutaneous tissue and small bowels. There was le
ss variability in MMP-1 and TIMP-1 protein content than mRNA expression; ov
aries and adhesions contained the highest MMP-1 and TIMP-1 levels, respecti
vely, and peritoneum contained the lowest. The MMP-1 and TIMP-1 content and
ratios further indicate limited MMP-1 proteolytic activity. Although tissu
es from premenopausal women express more MMP-1 and TIMP-1, expression did n
ot differ by sex or age.
Conclusion(s): Because MMP-1 and TIMP-1 expression varies consistently amon
g the serosal tissues of peritoneal organs and adhesions. and because tissu
e injury alters their expression, site-specific variations in expression of
these substances may predispose a particular organ to develop more adhesio
ns. (C) 2001 by American Society for Reproductive Medicine.