TY - JOUR
T1 - Transcription factor protein expression patterns by neural or neuronal progenitor cells of adult monkey subventricular zone
AU - Tonchev, A. B.
AU - Yamashima, T.
AU - Sawamoto, K.
AU - Okano, H.
N1 - Funding Information:
We thank Hirohide Takebayashi for the anti-Olig2 antibody and George N. Chaldakov for valuable discussions. The Japanese Ministries of Education, Culture, Sports, Science and Technology (Kiban B: 15390432) and Health, Labor and Welfare (H15-Kokoro-018), and the Bulgarian Ministry of Education and Science (L1311/03) supported this work.
PY - 2006
Y1 - 2006
N2 - 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), Dlx1,5 (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 Dlx2. Our results suggest that a complex network of developmental signals might be involved in the specification of primate progenitor cells.
AB - 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), Dlx1,5 (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 Dlx2. Our results suggest that a complex network of developmental signals might be involved in the specification of primate progenitor cells.
KW - adult neurogenesis
KW - cell fate
KW - cerebral ischemia
KW - developmental signal
KW - primate
UR - http://www.scopus.com/inward/record.url?scp=33646162856&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=33646162856&partnerID=8YFLogxK
U2 - 10.1016/j.neuroscience.2006.01.053
DO - 10.1016/j.neuroscience.2006.01.053
M3 - Article
C2 - 16580139
AN - SCOPUS:33646162856
SN - 0306-4522
VL - 139
SP - 1355
EP - 1367
JO - Neuroscience
JF - Neuroscience
IS - 4
ER -