TY - JOUR
T1 - Mapping spatio-temporal activation of Notch signaling during neurogenesis and gliogenesis in the developing mouse brain
AU - Tokunaga, Akinori
AU - Kohyama, Jun
AU - Yoshida, Tetsu
AU - Nakao, Keiko
AU - Sawamoto, Kazunobu
AU - Okano, Hideyuki
PY - 2004/7
Y1 - 2004/7
N2 - Notch1 plays various important roles including the maintenance of the stem cell state as well as the promotion of glial fates in mammalian CNS development. However, because of the very low amount of the activated form of Notch1 present in vivo, its precise activation pattern has remained unknown. In this study, we mapped the active state of this signaling pathway in situ in the developing mouse brain using a specific antibody that recognizes the processed form of the intracellular domain of Notch1 cleaved by presenilin/γ-secretase activity. By using this antibody, active state of Notch1 came to be detectable with a higher sensitivity than using conventional antibody against Notch1. We found that activated Notch1 was mainly detected in the nuclei of a subpopulation of radial glial cells, the majority of proliferating precursor cells in the ventricular zone (VZ). However, Notch1 activation was not detected in neuronal precursor cells positive for neuronal basic helix-loop-helix proteins or in differentiating neurons in the embryonic forebrain. Interestingly, we found that Notch1 was transiently activated in the astrocytic lineage during perinatal CNS development. Taken together, the present method has enabled us to determine the timing, gradients, and boundaries of the activation of Notch signaling.
AB - Notch1 plays various important roles including the maintenance of the stem cell state as well as the promotion of glial fates in mammalian CNS development. However, because of the very low amount of the activated form of Notch1 present in vivo, its precise activation pattern has remained unknown. In this study, we mapped the active state of this signaling pathway in situ in the developing mouse brain using a specific antibody that recognizes the processed form of the intracellular domain of Notch1 cleaved by presenilin/γ-secretase activity. By using this antibody, active state of Notch1 came to be detectable with a higher sensitivity than using conventional antibody against Notch1. We found that activated Notch1 was mainly detected in the nuclei of a subpopulation of radial glial cells, the majority of proliferating precursor cells in the ventricular zone (VZ). However, Notch1 activation was not detected in neuronal precursor cells positive for neuronal basic helix-loop-helix proteins or in differentiating neurons in the embryonic forebrain. Interestingly, we found that Notch1 was transiently activated in the astrocytic lineage during perinatal CNS development. Taken together, the present method has enabled us to determine the timing, gradients, and boundaries of the activation of Notch signaling.
KW - Activated Notch1
KW - Gliogenesis
KW - Mash1
KW - Neurogenesis
KW - Neurogenin2
KW - Radial glia
UR - http://www.scopus.com/inward/record.url?scp=3042729683&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=3042729683&partnerID=8YFLogxK
U2 - 10.1111/j.1471-4159.2004.02470.x
DO - 10.1111/j.1471-4159.2004.02470.x
M3 - Article
C2 - 15198674
AN - SCOPUS:3042729683
SN - 0022-3042
VL - 90
SP - 142
EP - 154
JO - Journal of Neurochemistry
JF - Journal of Neurochemistry
IS - 1
ER -