Regulation of hippocampal progenitor cell survival, proliferation and dendritic development by BDNF

被引:92
作者
Choi, Se Hoon [1 ]
Li, Yun [3 ,4 ]
Parada, Luis F. [3 ,4 ]
Sisodia, Sangram S. [1 ,2 ]
机构
[1] Univ Chicago, Comm Neurobiol, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Neurobiol, Chicago, IL 60637 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Dev Biol, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Kent Waldrep Ctr Basic Res Nerve Growth & Regener, Dallas, TX 75390 USA
关键词
NEUROTROPHIC FACTOR BDNF; GROWTH-FACTOR-I; DENTATE GYRUS; ENVIRONMENTAL ENRICHMENT; KNOCKOUT MICE; CONDITIONAL DELETION; DIETARY RESTRICTION; ADULT NEUROGENESIS; RAT-BRAIN; EXERCISE;
D O I
10.1186/1750-1326-4-52
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Environmental enrichment (EE) is known to enhance BDNF levels and neurogenesis in the adult hippocampus. To examine the role of BDNF in modulating EE-mediated adult hippocampal neurogenesis, we conditionally ablated BDNF expression in the hippocampus (cKO mice) and have assessed proliferation, survival, differentiation and dendritic development of hippocampal progenitors. Results: We show that while the extent of cell proliferation and neuronal fate differentiation in the hippocampus of cKO mice is not different from wild-type (WT) littermates maintained in either standard or enriched conditions, reduced BDNF levels significantly impaired the survival of newborn cells in both housing conditions. In addition, while highly active enriched WT mice exhibited a robust increase in progenitor cell proliferation, highly active cKO mice showed a modest increase in cell proliferation compared to standard housed or underactive cKO mice. Conclusions: There results argue that while BDNF plays a role in exercise-induced cell proliferation, other factors must contribute to this phenomenon. We also show that dendritic development was impaired in cKO mice maintained in standard housing conditions, and that EE rescued this phenotype.
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页数:12
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