Migration patterns of subventricular zone cells in adult mice change after cerebral cortex injury

被引:184
作者
Goings, GE [1 ]
Sahni, V [1 ]
Szele, FG [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Childrens Mem Hosp, CMIER Neurobiol Program,Dept Pediat, Chicago, IL 60614 USA
关键词
repair; plasticity; neurogenesis; lineage; retrovirus; SVZ; CD-1;
D O I
10.1016/j.brainres.2003.10.034
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The subventricular zone (SVZ) generates the largest number of migratory cells in the adult brain. SVZ neuroblasts migrate to the olfactory bulbs (OB) in the adult, whereas during development, SVZ cells migrate into many adjacent nuclei. Previously, we showed that cerebral cortex injury in the adult causes molecular and cellular changes which may recapitulate the developmental migratory directions. Consistent with this, growth factors, as well as models of illness or injury can cause adult SVZ cells to migrate into non-olfactory bulb nuclei. Here, we tested the hypothesis that cerebral cortex injury in the adult mouse induces changes in migration, by labeling adult SVZ cells with a retroviral vector and examining the distribution of cells 4 days and 3 weeks later. Four days after cortical lesions, disproportionately fewer retrovirally-labeled cells had migrated to the olfactory bulb in lesioned mice than in controls. Conversely, the number of cells found in non-olfactory bulb regions (primarily the area of the lesion and the corpus callosum) was increased in lesioned mice. The morphology of these emigrated cells suggested that they were differentiating into glial cells. Three weeks after cortical injury, the majority of retrovirally-labeled cells in both groups of mice had migrated into the granule and perigiomerular layers of the olfactory bulb. At 3 weeks, we still observed retrovirally-labeled glial cells in the corpus callosum and in the area of the injury in lesioned mice. These results suggest that cortical lesions cause a transient change in migration patterns of SVZ progeny, which is characterized by decreases in migration to the olfactory bulb but increased migration towards the injury. Our studies also suggest that cortical lesions induce the production of new glial cells which survive for at least 3 weeks after injury. The data support the concept that in the adult, SVZ cells can generate progeny that migrate towards injured areas and thus potentially be harnessed for neural repair. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:213 / 226
页数:14
相关论文
共 60 条
[1]  
Alonso G, 1999, J COMP NEUROL, V405, P508, DOI 10.1002/(SICI)1096-9861(19990322)405:4<508::AID-CNE5>3.0.CO
[2]  
2-5
[3]   Interneuron migration from basal forebrain to neocortex: Dependence on Dlx genes [J].
Anderson, SA ;
Eisenstat, DD ;
Shi, L ;
Rubenstein, JLR .
SCIENCE, 1997, 278 (5337) :474-476
[4]  
Behar TN, 1996, J NEUROSCI, V16, P1808
[5]   GABAB receptors mediate motility signals for migrating embryonic cortical cells [J].
Behar, TN ;
Smith, SV ;
Kennedy, RT ;
Mckenzie, JM ;
Maric, I ;
Barker, AL .
CEREBRAL CORTEX, 2001, 11 (08) :744-753
[6]   Adenoviral brain-derived neurotrophic factor induces both neostriatal and olfactory neuronal recruitment from endogenous progenitor cells in the adult forebrain [J].
Benraiss, A ;
Chmielnicki, E ;
Lerner, K ;
Roh, D ;
Goldman, SA .
JOURNAL OF NEUROSCIENCE, 2001, 21 (17) :6718-6731
[7]   Newly generated neurons in the amygdala and adjoining cortex of adult primates [J].
Bernier, PJ ;
Bédard, A ;
Vinet, J ;
Lévesque, M ;
Parent, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (17) :11464-11469
[8]   Control of cell migration during Caenorhabditis elegans development [J].
Blelloch, R ;
Newman, C ;
Kimble, J .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (05) :608-613
[9]   Proliferation and phenotype regulation in the subventricular zone during experimental allergic encephalomyelitis:: In vivo evidence of a role for nerve growth factor [J].
Calzà, L ;
Giardino, L ;
Pozza, M ;
Bettelli, C ;
Micera, A ;
Aloe, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (06) :3209-3214
[10]   Lineage analysis using retroviral vectors [J].
Cepko, CL ;
Ryder, E ;
Austin, C ;
Golden, J ;
Fields-Berry, S ;
Lin, J .
METHODS-A COMPANION TO METHODS IN ENZYMOLOGY, 1998, 14 (04) :393-406