TY - JOUR
T1 - Regulation of cortical neuron migration by the reelin signaling pathway
AU - Honda, Takao
AU - Kobayashi, Kazuma
AU - Mikoshiba, Katsuhiko
AU - Nakajima, Kazunori
N1 - Funding Information:
Acknowledgments This work was supported by the Strategic Research Program for Brain Sciences (‘‘Understanding of molecular and environmental bases for brain health’’), the Ministry of Education, Culture, Sports, Science, and Technology of Japan, the Japan Society for the Promotion of Science, the Japan Brain Foundation, the Takeda Science Foundation, the Keio Gijuku Academic Development Funds, and the Promotion and Mutual Aid Corporation for Private Schools of Japan.
PY - 2011/7
Y1 - 2011/7
N2 - Reeler is a mutant mouse with defects in layered structures of the central nervous system, such as the cerebral cortex, hippocampus, and cerebellum, and has been extensively examined for more than half a century. The full-length cDNA for the responsible gene for reeler, reelin, was serendipitously identified, revealing that Reelin encodes a large secreted protein. So far, two Reelin receptors, apolipoprotein E receptor 2 and very low-density lipoprotein receptor, and the cytoplasmic adaptor protein Disabled homolog 1 (Dab1) have been shown to be essential for Reelin signaling. Although a number of downstream cascades of Dab1 have also been reported using various experimental systems, the physiological functions of Reelin in vivo remain controversial. Here, we review recent advances in the understanding of the Reelin-Dab1 signaling pathway in the developing cerebral cortex.
AB - Reeler is a mutant mouse with defects in layered structures of the central nervous system, such as the cerebral cortex, hippocampus, and cerebellum, and has been extensively examined for more than half a century. The full-length cDNA for the responsible gene for reeler, reelin, was serendipitously identified, revealing that Reelin encodes a large secreted protein. So far, two Reelin receptors, apolipoprotein E receptor 2 and very low-density lipoprotein receptor, and the cytoplasmic adaptor protein Disabled homolog 1 (Dab1) have been shown to be essential for Reelin signaling. Although a number of downstream cascades of Dab1 have also been reported using various experimental systems, the physiological functions of Reelin in vivo remain controversial. Here, we review recent advances in the understanding of the Reelin-Dab1 signaling pathway in the developing cerebral cortex.
KW - ApoER2
KW - Dab1
KW - Reeler
KW - Reelin
KW - VLDLR
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U2 - 10.1007/s11064-011-0407-4
DO - 10.1007/s11064-011-0407-4
M3 - Review article
C2 - 21253854
AN - SCOPUS:79959889039
SN - 0364-3190
VL - 36
SP - 1270
EP - 1279
JO - Neurochemical Research
JF - Neurochemical Research
IS - 7
ER -