TY - JOUR
T1 - Expression of the basic helix-loop-factor Olig2 in the developing retina
T2 - Olig2 as a new marker for retinal progenitors and late-born cells
AU - Shibasaki, Koji
AU - Takebayashi, Hirohide
AU - Ikenaka, Kazuhiro
AU - Feng, Liang
AU - Gan, Lin
N1 - Funding Information:
We thank Drs. K. Ono, M. Furusho and K. Ikeda for technical assistance, Drs. K. Ono, S.-I. Watanabe and F. Tamalu for discussion and critical reading of manuscripts, Dr. J. Miyazaki for providing us CAG-CAT-Z mice, and Dr. M. Tominaga and his lab members for encouragement. The monoclonal antibodies, G3G4, Pax6, 39.4D5 and GAD6, developed by Drs. S.J. Kaufman, A. Kawakami, T.M. Jessell and D.I. Gottlieb were obtained from the Developmental Studies Hybridoma Bank maintained by the University of Iowa, Department of Biological Sciences. This work was supported by Tokai Gakujyutsu Scientific Grants awarded to K.S., and NIH-NEI Grants EY013426 and EY015551 awarded to L.G.
PY - 2007/1
Y1 - 2007/1
N2 - In this study, we examined the spatiotemporal expression patterns of Olig2, a basic helix-loop-helix transcription factor, in the developing mouse retina. Expression of Olig2 was initially detected on embryonic day 12.5 (E12.5). The majority of Olig2-positive cells were identified as retinal progenitor cells throughout embryogenesis. During later embryonic stages, the number of Olig2-positive retinal progenitor cells increased, and Olig2-positive cells were confined only to the neuroblast layer (NBL). Olig2 expression was not observed in the ganglion cell layer (GCL) nor in the inner nuclear layer (INL) that contain the differentiated retinal cell types, indicating that Olig2 is not expressed in differentiated cells in prenatal retina. In later postnatal stages, Olig2 expression was retained in mature neurons and glial cells, namely retinal ganglion cells (RGCs), amacrine cells (ACs), horizontal cells, bipolar cells and Müller glial cells. Thus, Olig2 is an marker both for retinal progenitor cells during embryonic stages, and also for differentiated retinal subpopulations within the GCL and INL during postnatal stages.
AB - In this study, we examined the spatiotemporal expression patterns of Olig2, a basic helix-loop-helix transcription factor, in the developing mouse retina. Expression of Olig2 was initially detected on embryonic day 12.5 (E12.5). The majority of Olig2-positive cells were identified as retinal progenitor cells throughout embryogenesis. During later embryonic stages, the number of Olig2-positive retinal progenitor cells increased, and Olig2-positive cells were confined only to the neuroblast layer (NBL). Olig2 expression was not observed in the ganglion cell layer (GCL) nor in the inner nuclear layer (INL) that contain the differentiated retinal cell types, indicating that Olig2 is not expressed in differentiated cells in prenatal retina. In later postnatal stages, Olig2 expression was retained in mature neurons and glial cells, namely retinal ganglion cells (RGCs), amacrine cells (ACs), horizontal cells, bipolar cells and Müller glial cells. Thus, Olig2 is an marker both for retinal progenitor cells during embryonic stages, and also for differentiated retinal subpopulations within the GCL and INL during postnatal stages.
KW - Basic helix-loop-helix
KW - Cell specification
KW - Development
KW - Differentiation
KW - Homeobox
KW - Neurogenesis
KW - Olig2
KW - Progenitor
KW - Retina
KW - Transcription factor
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U2 - 10.1016/j.modgep.2006.05.008
DO - 10.1016/j.modgep.2006.05.008
M3 - Article
C2 - 16815098
AN - SCOPUS:33750796652
SN - 1567-133X
VL - 7
SP - 57
EP - 65
JO - Brain research. Gene expression patterns
JF - Brain research. Gene expression patterns
IS - 1-2
ER -