Postnatal deletion of numb/numblike reveals repair and remodeling capacity in the subventricular neurogenic niche

被引:174
作者
Kuo, Chay T.
Mirzadeh, Zaman
Soriano-Navarro, Mario
Rasin, Mladen
Wang, Denan
Shen, Jie
Sestan, Nenad
Garcia-Verdugo, Jose
Alvarez-Buylla, Arturo
Jan, Lily Y.
Jan, Yuh-Nung [1 ]
机构
[1] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Physiol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, Dept Biochem, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Neurol Surg, Program Dev & Stem Cell Biol, San Francisco, CA 94143 USA
[4] Univ Valencia, Unidad Asociada Ctr Invest Principe Felipe, Lab Morfol Celular, Valencia 46013, Spain
[5] Yale Univ, Sch Med, Dept Neurobiol, New Haven, CT 06510 USA
[6] Yale Univ, Sch Med, Kavli Inst Neurosci, New Haven, CT 06510 USA
[7] Harvard Univ, Sch Med, Brigham & Womens Hosp, Ctr Neurol Dis, Boston, MA 02115 USA
关键词
D O I
10.1016/j.cell.2006.10.041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Neural stem cells are retained in the postnatal subventricular zone (SVZ), a specialized neurogenic niche with unique cytoarchitecture and cell-cell contacts. Although the SVZ stem cells continuously regenerate, how they and the niche respond to local changes is unclear. Here we generated nestin-creER(tm) transgenic mice with inducible Cre recombinase in the SVZ and removed Numb/Numblike, key regulators of embryonic neurogenesis from postnatal SVZ progenitors and ependymal cells. This resulted in severe damage to brain lateral ventricle integrity and identified roles for Numb/Numblike in regulating ependymal wall integrity and SVZ neuroblast survival. Surprisingly, the ventricular damage was eventually repaired: SVZ reconstitution and ventricular wall remodeling were mediated by progenitors that escaped Numb deletion. Our results show a self-repair mechanism in the mammalian brain and may have implications for both niche plasticity in other areas of stem cell biology and the therapeutic use of neural stem cells in neurodegenerative diseases.
引用
收藏
页码:1253 / 1264
页数:12
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