Early determination and long-term persistence of adult-generated new neurons in the hippocampus of mice

被引:785
作者
Kempermann, G
Gast, D
Kronenberg, G
Yamaguchi, M
Gage, FH
机构
[1] Max Delbruck Ctr Mol Med, D-13125 Berlin, Germany
[2] Humboldt Univ, Charite Univ Hosp, Dept Expt Neurol, Volkswagenstiftung Res Grp, D-10117 Berlin, Germany
[3] Free Univ Berlin, Dept Psychiat, D-14050 Berlin, Germany
[4] Univ Tokyo, Grad Sch Med, Dept Physiol, Bunkyo Ku, Tokyo 1130033, Japan
[5] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
来源
DEVELOPMENT | 2003年 / 130卷 / 02期
关键词
stem cell; progenitor cell; adult neurogenesis; mouse;
D O I
10.1242/dev.00203
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
New neurons are continually generated in the adult hippocampus, but the important question, whether adult neurogenesis is transient or leads to the lasting presence of new neurons, has not yet been answered. Dividing cells were labeled with bromodeoxyuridine (BrdU) and were investigated by means of immunofluorescence and confocal microscopy at several time-points 1 day to 11 months thereafter. BrdU-labeled neurons remained stable in number and in their relative position in the granule cell layer over at least 11 months. This finding implies that the addition of new neurons is not transient and that their final number and localization are determined early. By contrast, expression of immature markers beta-III-tubulin and doublecortin in BrdU-labeled cells, peaked early after division and was not detectable after 4 weeks. In transgenic mice expressing enhanced green fluorescent protein under the nestin promoter none of the BrdU/nestin-positive cells early after division expressed the mature marker NeuN, confirming that no dividing neurons were detected. These new data suggest that new neurons are recruited early from the pool of proliferating progenitor cells and lead to a lasting effect of adult neurogenesis.
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页码:391 / 399
页数:9
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