Neural Stem and Progenitor Cells Retain Their Potential for Proliferation and Differentiation into Functional Neurons Despite Lower Number in Aged Brain

被引:157
作者
Ahlenius, Henrik [1 ,4 ]
Visan, Violeta [2 ,4 ]
Kokaia, Merab [3 ]
Lindvall, Olle [2 ,4 ]
Kokaia, Zaal [1 ,4 ]
机构
[1] Univ Lund Hosp, Lab Neural Stem Cell Biol, Sect Restorat Neurol, Wallenberg Neurosci Ctr, SE-22184 Lund, Sweden
[2] Univ Lund Hosp, Lab Neurogenesis & Cell Therapy, Sect Restorat Neurol, Wallenberg Neurosci Ctr, SE-22184 Lund, Sweden
[3] Univ Lund Hosp, Expt Epilepsy Grp, Sect Restorat Neurol, Wallenberg Neurosci Ctr, SE-22184 Lund, Sweden
[4] Lund Stem Cell Ctr, SE-22184 Lund, Sweden
基金
瑞典研究理事会;
关键词
SUBVENTRICULAR ZONE; OLD-AGE; HIPPOCAMPAL NEUROGENESIS; STEM/PROGENITOR CELLS; POTASSIUM CURRENT; DENTATE GYRUS; GRANULE CELLS; K+ CHANNELS; G(1) PHASE; IN-VITRO;
D O I
10.1523/JNEUROSCI.6003-08.2009
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurogenesis in the subventricular zone (SVZ), which gives rise to new neurons in the olfactory bulb, continues throughout life but declines with increasing age. Little is known about how aging affects the intrinsic properties of the neural stem and progenitor cells (NSCs) in SVZ and the functional characteristics of their neuronal progeny. Here, we have compared the properties of NSCs isolated from embryonic lateral ganglionic eminence and adult and aged SVZ in mice using in vivo and in vitro systems, analyzed their gene expression profile, and studied their electrophysiological characteristics before and after differentiation into neurons. We show a loss of NSCs in SVZ from aged mice accompanied by reduced expression of genes for NSC markers, developmentally important transcription factors, and neurogenic factors. However, when isolated in vitro, the NSCs from SVZ of aged animals have capacity for proliferation and multilineage differentiation, including production of functional neurons, similar to that of NSCs in adult mice, albeit with lower efficacy. These properties are of major importance when considering therapeutic applications of neuronal replacement from endogenous NSCs in the injured, aged brain.
引用
收藏
页码:4408 / 4419
页数:12
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