Transcription factor protein expression patterns by neural or neuronal progenitor cells of adult monkey subventricular zone

被引:28
|
作者
Tonchev, A. B.
Yamashima, T.
Sawamoto, K.
Okano, H.
机构
[1] Kanazawa Univ, Grad Sch Med Sci, Div Neurosci, Dept Restorat Neurosurg, Kanazawa, Ishikawa 9208641, Japan
[2] Varna Univ Med, Dept Forens Med, Div Cell Biol, BG-9002 Varna, Bulgaria
[3] Keio Univ, Sch Med, Bridgestone Lab Dev & Regenerat Neurobiol, Tokyo, Japan
[4] Keio Univ, Sch Med, Dept Physiol, Tokyo 160, Japan
关键词
cerebral ischemia; primate; adult neurogenesis; cell fate; developmental signal;
D O I
10.1016/j.neuroscience.2006.01.053
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The anterior subventricular zone of the adult mammalian brain contains progenitor cells which are upregulated after cerebral ischemia. We have previously reported that while a part of the progenitors residing in adult monkey anterior subventricular zone travels to the olfactory bulb, many of these cells sustain location in the anterior subventricular zone for months after injury, exhibiting a phenotype of either neural or neuronal precursors. Here we show that ischemia increased the numbers of anterior subventricular zone progenitor cells expressing developmentally regulated transcription factors including Pax6 (paired-box 6), Emx2 (empty spiracles-homeobox 2), Sox 1-3 (sex determining region Y-box 1-3), Ngn1 (neurogenin 1), DIx1,5 (distalless-homeobox 1,5), Olig1,3 (oligodendrocyte lineage gene 1,3) and Nkx2.2 (Nk-box 2.2), as compared with control brains. Analysis of transcription factor protein expression by sustained neural or neuronal precursors in anterior subventricular zone revealed that these two cell types were positive for characteristic sets of transcription factors. The proteins Pax6, Emx2, Sox2,3 and Olig1 were predominantly localized to dividing neural precursors while the factors Sox1, Ngn1, Dlx1,5, Olig2 and Nkx2.2 were mainly expressed by neuronal precursors. Further, differences between monkeys and non-primate mammals emerged, related to expression patterns of Pax6, Olig2 and DIx2. Our results suggest that a complex network of developmental signals might be involved in the specification of primate progenitor cells. (c) 2006 Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:1355 / 1367
页数:13
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