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Comparison of AT8 immunoreactivity in the locus ceruleus and hippocampus of 154 brains from routine autopsies.

Authors :
Okamoto K
Amari M
Fukuda T
Suzuki K
Takatama M
Source :
Neuropathology : official journal of the Japanese Society of Neuropathology [Neuropathology] 2017 Aug; Vol. 37 (4), pp. 306-310. Date of Electronic Publication: 2017 Feb 06.
Publication Year :
2017

Abstract

We compared semiquantitatively AT8 immunoreactivity in the locus ceruleus (LC) and hippocampus of 154 brains from routine autopsies to investigate the initial sites of phosphorylated tau (phospho-tau) development. The numbers of AT8-positive neurons and the severity of AT8-positive neuropil threads (NTs) in the LC were strongly associated: there were no cases with AT8-positive neurons that lacked NTs and 20 cases (13%) had only NTs in the LC. Phospho-tau pathologies in the LC were almost equally on both sides, although some cases (7.8%) showed unilateral predominance. The numbers of AT8-positive neurons in the LC and the numbers of AT8-positive neurons and NTs in the hippocampus were also strongly associated. There were only two cases with AT8-positive neurons in the LC that lacked phospho-tau pathology in the hippocampus, and 21 cases (13.6%) with phospho-tau pathology in the hippocampus that lacked AT8-positive neurons in the LC. The numbers of AT8-positive NTs in the LC and AT8-positive neurons and NTs in the hippocampus were also strongly associated. There were seven cases (4.5%) with AT8-positive NTs in the LC that lacked phospho-tau pathology in the hippocampus, and five cases (3.2 %) with phospho-tau pathologies in the hippocampus that lacked AT8-positive NTs in the LC. In this study, we could not confirm that phospho-tau pathologies begin in the LC. We suspect their simultaneous occurrences in both hippocampal regions and in LC.<br /> (© 2017 Japanese Society of Neuropathology.)

Details

Language :
English
ISSN :
1440-1789
Volume :
37
Issue :
4
Database :
MEDLINE
Journal :
Neuropathology : official journal of the Japanese Society of Neuropathology
Publication Type :
Academic Journal
Accession number :
28168741
Full Text :
https://doi.org/10.1111/neup.12367