A growing amount of evidence indicates that matrix metalloproteinases (MMPs
) may play an important role in the pathogenesis of Alzheimer's disease (AD
). Stromelysin-1 (MMP-3) plays a central role in activating latent-type MMP
s, which are originally secreted as preen zymes. We examined MMP-3 immunore
activity in the brains of patients who had suffered from Alzheimer's diseas
e and in those of neurologically normal persons. The interstitium between m
yelinated axons and astrocytes in the white matter of all brain tissues, an
d senile plaques in the gray matter of the patients with AD were stained wi
th a monoclonal antibody to MMP-3. Comparison of the number of senile plaqu
es stained with the antibody against MMP-3 in the parietal cortex with that
in the hippocampus showed that fewer plaques were stained in the hippocamp
us. The selective distribution of MMP-3 in the human brain suggests that MM
P-3 might play an important role in the pathogenesis of AD, especially in t
he degradation of beta-amyloid protein.