The generation of oligodendroglial cells is preserved in the rostral migratory stream during aging

被引:39
作者
Capilla-Gonzalez, Vivian [1 ]
Cebrian-Silla, Arantxa [2 ]
Guerrero-Cazares, Hugo [1 ]
Garcia-Verdugo, Jose M. [2 ]
Quinones-Hinojosa, Alfredo [1 ]
机构
[1] Johns Hopkins Sch Med, Brain Tumor Stem Cell Lab, Dept Neurosurg, Baltimore, MD USA
[2] Univ Valencia, Inst Cavanilles Biodiversidad & Biol Evolut, Lab Comparat Neurobiol, CIBERNED, Valencia, Spain
基金
美国国家卫生研究院;
关键词
neuroblast migration; subventricular zone; rostral migratory stream; olfactory bulb; neurogenesis; oligodendrogenesis; aging; NEURAL STEM-CELLS; SUBVENTRICULAR ZONE; OLFACTORY-BULB; CELLULAR COMPOSITION; PROGENITOR CELLS; HUMAN BRAIN; AGE; NEUROGENESIS; NEUROBLASTS; NEURONS;
D O I
10.3389/fncel.2013.00147
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The subventricular zone (SVZ) is the largest source of newly generated cells in the adult mammalian brain. SVZ-derived neuroblasts migrate via the rostral migratory stream (RMS) to the olfactory bulb (OB), where they differentiate into mature neurons. Additionally, a small proportion of SVZ-derived cells contribute to the generation of myelinating oligodendrocytes. The production of new cells in the SVZ decreases during aging, affecting the incorporation of new neurons into the OB. However, the age-related changes that occur across the RMS are not fully understood. In this study we evaluate how aging affects the cellular organization of migrating neuroblast chains, the proliferation, and the fate of the newly generated cells in the SVZ-OB system. By using electron microscopy and immunostaining, we found that the RMS path becomes discontinuous and its cytoarchitecture is disorganized in aged mice (24-month-old mice). Subsequently, OB neurogenesis was impaired in the aged brain while the production of oligodendrocytes was not compromised. These findings provide new insight into oligodendrocyte preservation throughout life. Further exploration of this matter could help the development of new strategies to prevent neurological disorders associated with senescence.
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页数:9
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