Expression of embryonic tau protein isoforms persist during adult neurogenesis in the hippocampus

被引:48
作者
Bullmann, Torsten
de Silva, Rohan
Holzer, Max
Mori, Hiroshi
Arendt, Thomas
机构
[1] Univ Leipzig, Paul Flechsig Inst Brain Res, Dept Neuroanat, D-04109 Leipzig, Germany
[2] UCL, Reta Lila Weston Inst Neurol Studies, London, England
[3] Osaka City Univ, Sch Med, Abeno Ku, Osaka 558, Japan
基金
英国医学研究理事会;
关键词
development; neuronal differentiation; neuronal plasticity; hippocampus; neurodegeneration;
D O I
10.1002/hipo.20255
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tau is a microtubule-associated protein with a developmentally regulated expression of multiple isoforms. The neonatal isoform is devoid of two amino terminal inserts and contains only three instead of four microtubuie-binding repeats (0N/3R-tau). We investigated the temporal expression pattern of 0N-tau and 3R-tau in the rat hippocampus. After the decline of 0N-tau and 3R-tau immunoreactivity during the postnatal development both isoforms remain highly expressed in a few cells residing beneath the granule cell layer. Coexpression of the polysialylated neuronal cell adhesion molecule, doublecortin, and incorporated bromode-oxyuridine showed that these cells are proliferating progenitor cells. in contrast mature granule cells express the adult tau protein isoform containing one aminoterminal insert domain (1N-tau). Therefore a shift in tau isoform expression takes place during adult neurogenesis, which might be related to migration, differentiation, and integration in the granule cell layer. A model for studying shifts in tau isoform expression in a defined subset of neurons might help to understand the etiology of tauopathies, when isoform composition is crucial for neurodegeneration, as in Pick's disease or FTDP-17. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:98 / 102
页数:5
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