Failure of neuronal maturation in Alzheimer disease dentate gyrus

被引:201
作者
Li, Bin [1 ]
Yamamori, Hidenaga [1 ]
Tatebayashi, Yoshitaka [1 ]
Shafit-Zagardo, Bridget [2 ]
Tanimukai, Hitoshi [1 ]
Chen, She [1 ]
Iqbal, Khalid [1 ]
Grundke-Iqbal, Inge [1 ]
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Neurochem, Staten Isl, NY 10314 USA
[2] Albert Einstein Coll Med, Dept Pathol, Bronx, NY 10467 USA
关键词
Alzheimer disease; hippocampus; microtubule-associated; protein; 2; neurogenesis;
D O I
10.1097/nen.0b013e318160c5db
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The dentate gyrus, an important anatomic structure of the hippocampal formation, is one of the major areas in which neurogenesis takes place in the adult mammalian brain. Neurogenesis in the dentate gyrus is thought to play an important role in hippocampus-dependent learning and memory. Neurogenesis has been reported to be increased in the dentate gyrus of patients with Alzheimer disease, but it is not known whether the newly generated neurons differentiate into mature neurons. In this study, the expression of the mature neuronal marker high molecular weight microtubule-associated protein (MAP) isoforms MAP2a and b was found to be dramatically decreased in Alzheimer disease dentate gyrus, as determined by immunohistochemistry and in situ hybridization. The total MAP2, including expression of the immature neuronal marker, the MAP2c isoform, was less affected. These findings suggest that newly generated neurons in Alzheimer disease dentate gyrus do not become mature neurons, although neuroproliferation is increased.
引用
收藏
页码:78 / 84
页数:7
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