alphaB-crystallin is known as a small heat shock protein with a cytoprotect
ive function. This study was undertaken to investigate the relationship bet
ween alphaB-crystallin and changes seen in Alzheimer's disease. The distrib
ution and immunohistochemical characteristics of alphaB-crystallin positive
neurones in the cerebral cortices of 4 patients with Alzheimer's disease w
ere examined. alphaB-crystallin positive neurones were mainly distributed i
n the limbic and paralimbic regions, namely parahippocampal gyrus, fusiform
gyrus, cingulate cortex, middle and superior frontal gyrus, and insular co
rtex, which corresponded to commonly affected regions in Alzheimer's diseas
e. Moreover, such neurones were present predominantly in the III or V layer
of the cerebral cortex. The number of alphaB-crystallin positive neurones
increased in parallel with the neuronal loss. Logistic regression analysis
revealed a significant relation between the density of alphaB-crystallin po
sitive neurones and that of extracellular neurofibrillary tangles (NFTs), w
ith a correlation coefficient (r) of 0.57 and P < 0.0001 in 14 regions of t
he cerebral cortex. In contrast, the relation was not statistically signifi
cant between the density of alphaB-crystallin positive neurones and that of
classical senile plaques, diffuse plaques or intracellular NFTs. Modified
Gallyas-Braak (GB) staining on alphaB-crystallin positive neurone demonstra
ted several patterns of the structures: faint GB positive structures in the
swollen perikaryon with straight neurites, fine granules compressed and co
ntorted into fuzzy bundles, intensely GB positive filamentous structures to
gether with fine granules and very intensely GB positive ring-like NFTs in
a swollen perikaryon with curved neurites. In positive neurones, the densit
y of ring-like NFTs correlated with that of atrophic perikaryon, or bent ne
urites and a decrease in the immuoreactivity of alphaB-crystallin. These da
ta suggest that a close relationship exists between the appearance of alpha
B-crystallin in neurones, extracellular NFTs, and neurofibrillary formation
in alphaB-crystallin positive neurones in Alzheimer brain.