TY - JOUR
T1 - A novel population of hopx-dependent basal radial glial cells in the developing mouse neocortex
AU - Vaid, Samir
AU - Camp, J. Gray
AU - Hersemann, Lena
AU - Oegema, Christina Eugster
AU - Heninger, Anne Kristin
AU - Winkler, Sylke
AU - Brandl, Holger
AU - Sarov, Mihail
AU - Treutlein, Barbara
AU - Huttner, Wieland B.
AU - Namba, Takashi
N1 - Publisher Copyright:
© 2018. Published by The Company of Biologists Ltd.
PY - 2018
Y1 - 2018
N2 - A specific subpopulation of neural progenitor cells, the basal radial glial cells (bRGCs) of the outer subventricular zone (OSVZ), are thought to have a key role in the evolutionary expansion of the mammalian neocortex. In the developing lissencephalic mouse neocortex, bRGCs exist at low abundance and show significant molecular differences from bRGCs in developing gyrencephalic species. Here, we demonstrate that the developing mouse medial neocortex (medNcx), in contrast to the canonically studied lateral neocortex (latNcx), exhibits an OSVZ and an abundance of bRGCs similar to that in developing gyrencephalic neocortex. Unlike bRGCs in developing mouse latNcx, the bRGCs in medNcx exhibit human bRGC-like gene expression, including expression of Hopx, a human bRGC marker. Disruption of Hopx expression in mouse embryonic medNcx and forced Hopx expression in mouse embryonic latNcx demonstrate that Hopx is required and sufficient, respectively, for bRGC abundance as found in the developing gyrencephalic neocortex. Taken together, our data identify a novel bRGC subpopulation in developing mouse medNcx that is highly related to bRGCs of developing gyrencephalic neocortex.
AB - A specific subpopulation of neural progenitor cells, the basal radial glial cells (bRGCs) of the outer subventricular zone (OSVZ), are thought to have a key role in the evolutionary expansion of the mammalian neocortex. In the developing lissencephalic mouse neocortex, bRGCs exist at low abundance and show significant molecular differences from bRGCs in developing gyrencephalic species. Here, we demonstrate that the developing mouse medial neocortex (medNcx), in contrast to the canonically studied lateral neocortex (latNcx), exhibits an OSVZ and an abundance of bRGCs similar to that in developing gyrencephalic neocortex. Unlike bRGCs in developing mouse latNcx, the bRGCs in medNcx exhibit human bRGC-like gene expression, including expression of Hopx, a human bRGC marker. Disruption of Hopx expression in mouse embryonic medNcx and forced Hopx expression in mouse embryonic latNcx demonstrate that Hopx is required and sufficient, respectively, for bRGC abundance as found in the developing gyrencephalic neocortex. Taken together, our data identify a novel bRGC subpopulation in developing mouse medNcx that is highly related to bRGCs of developing gyrencephalic neocortex.
KW - Basal radial glial cell
KW - Development
KW - Evolution
KW - Hopx
KW - Neocortex
UR - https://www.scopus.com/pages/publications/85055202261
UR - https://www.scopus.com/pages/publications/85055202261#tab=citedBy
U2 - 10.1242/dev.169276
DO - 10.1242/dev.169276
M3 - Article
C2 - 30266827
AN - SCOPUS:85055202261
SN - 0950-1991
VL - 145
JO - Development (Cambridge)
JF - Development (Cambridge)
IS - 20
M1 - dev169276
ER -