TY - JOUR
T1 - Characterization of multiciliated ependymal cells that emerge in the neurogenic niche of the aged zebrafish brain
AU - Ogino, Takashi
AU - Sawada, Masato
AU - Takase, Hiroshi
AU - Nakai, Chiemi
AU - Herranz-Pérez, Vicente
AU - Cebrián-Silla, Arantxa
AU - Kaneko, Naoko
AU - García-Verdugo, José Manuel
AU - Sawamoto, Kazunobu
N1 - Publisher Copyright:
© 2016 Wiley Periodicals, Inc.
PY - 2016/10/15
Y1 - 2016/10/15
N2 - In mammals, ventricular walls of the developing brain maintain a neurogenic niche, in which radial glial cells act as neural stem cells (NSCs) and generate new neurons in the embryo. In the adult brain, the neurogenic niche is maintained in the ventricular-subventricular zone (V-SVZ) of the lateral wall of lateral ventricles and the hippocampal dentate gyrus. In the neonatal V-SVZ, radial glial cells transform into astrocytic postnatal NSCs and multiciliated ependymal cells. On the other hand, in zebrafish, radial glial cells continue to cover the surface of the adult telencephalic ventricle and maintain a higher neurogenic potential in the adult brain. However, the cell composition of the neurogenic niche of the aged zebrafish brain has not been investigated. Here we show that multiciliated ependymal cells emerge in the neurogenic niche of the aged zebrafish telencephalon. These multiciliated cells appear predominantly in the dorsal part of the ventral telencephalic ventricular zone, which also contains clusters of migrating new neurons. Scanning electron microscopy and live imaging analyses indicated that these multiple cilia beat coordinately and generate constant fluid flow within the ventral telencephalic ventricle. Analysis of the cell composition by transmission electron microscopy revealed that the neurogenic niche in the aged zebrafish contains different types of cells, with ultrastructures similar to those of ependymal cells, transit-amplifying cells, and migrating new neurons in postnatal mice. These data suggest that the transformation capacity of radial glial cells is conserved but that its timing is different between fish and mice. J. Comp. Neurol. 524:2982–2992, 2016.
AB - In mammals, ventricular walls of the developing brain maintain a neurogenic niche, in which radial glial cells act as neural stem cells (NSCs) and generate new neurons in the embryo. In the adult brain, the neurogenic niche is maintained in the ventricular-subventricular zone (V-SVZ) of the lateral wall of lateral ventricles and the hippocampal dentate gyrus. In the neonatal V-SVZ, radial glial cells transform into astrocytic postnatal NSCs and multiciliated ependymal cells. On the other hand, in zebrafish, radial glial cells continue to cover the surface of the adult telencephalic ventricle and maintain a higher neurogenic potential in the adult brain. However, the cell composition of the neurogenic niche of the aged zebrafish brain has not been investigated. Here we show that multiciliated ependymal cells emerge in the neurogenic niche of the aged zebrafish telencephalon. These multiciliated cells appear predominantly in the dorsal part of the ventral telencephalic ventricular zone, which also contains clusters of migrating new neurons. Scanning electron microscopy and live imaging analyses indicated that these multiple cilia beat coordinately and generate constant fluid flow within the ventral telencephalic ventricle. Analysis of the cell composition by transmission electron microscopy revealed that the neurogenic niche in the aged zebrafish contains different types of cells, with ultrastructures similar to those of ependymal cells, transit-amplifying cells, and migrating new neurons in postnatal mice. These data suggest that the transformation capacity of radial glial cells is conserved but that its timing is different between fish and mice. J. Comp. Neurol. 524:2982–2992, 2016.
KW - adult neurogenesis
KW - cilia
KW - ependymal cells
KW - neural stem cells
KW - neurogenic niche
KW - zebrafish
UR - https://www.scopus.com/pages/publications/84962787687
UR - https://www.scopus.com/pages/publications/84962787687#tab=citedBy
U2 - 10.1002/cne.24001
DO - 10.1002/cne.24001
M3 - Article
C2 - 26991819
AN - SCOPUS:84962787687
SN - 0021-9967
VL - 524
SP - 2982
EP - 2992
JO - Journal of Comparative Neurology
JF - Journal of Comparative Neurology
IS - 15
ER -