Visualization of Rostral Migratory Stream in the Developing Rat Brain by In Vivo Electroporation

被引:2
|
作者
Xie, Yi-wei [1 ]
Li, Zhao-yun [4 ]
Du, Jing [1 ]
Chen, Yu [1 ]
Chen, Bing-yu [1 ]
Wang, Tong-tong [1 ]
Huang, Zhihui [2 ]
Hou, Shuangxing [3 ]
Wang, Ying [1 ]
机构
[1] Peoples Hosp, Zhejiang Prov Peoples Hosp, Dept Transfus, Hangzhou Med Coll, Hangzhou 310014, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Inst Neurosci, Wenzhou 325035, Zhejiang, Peoples R China
[3] Fudan Univ, Pudong Med Ctr, ShanghaiPudong Hosp, Dept Neurol, 2800 Gongwei Rd, Shanghai 201399, Peoples R China
[4] Taizhou Univ Hosp, Taizhou Cent Hosp, Dept Clin Lab, Taizhou 318000, Zhejiang, Peoples R China
关键词
Olfactory bulb; Rostral migratory stream; Interneurons; Migration; In vivo electroporation; OLFACTORY-BULB INTERNEURONS; SUBVENTRICULAR ZONE; NEURONAL MIGRATION; CELL-MIGRATION; UTERO ELECTROPORATION; NEUROBLAST MIGRATION; POSTNATAL BRAIN; GENE-EXPRESSION; ADULT BRAIN; FOREBRAIN;
D O I
10.1007/s10571-018-0577-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Interneurons in the olfactory bulb (OB) are generated from neuronal precursor cells migrating from anterior subventricular zone (SVZa) not only in the developing embryo but also throughout the postnatal life of mammals. In the present study, we established an in vivo electroporation assay to label SVZa cells of rat both at embryonic and postnatal ages, and traced SVZa progenitors and followed their migration pathway and differentiation. We found that labeled cells displayed high motility. Interestingly, the postnatal cells migrated faster than the embryonic cells after applying this assay at different ages of brain development. Furthermore, based on brain slice culture and time-lapse imaging, we analyzed the detail migratory properties of these labeled precursor neurons. Finally, tissue transplantation experiments revealed that cells already migrated in subependymal zone of OB were transplanted back into rostral migratory stream (RMS), and these cells could still migrate out tangentially along RMS to OB. Taken together, these findings provide an in vivo labeling assay to follow and trace migrating cells in the RMS, their maturation and integration into OB neuron network, and unrecognized phenomena that postnatal SVZa progenitor cells with higher motility than embryonic cells, and their migration was affected by extrinsic environments.
引用
收藏
页码:1067 / 1079
页数:13
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