Canonical and noncanonical Wnt signaling in neural stem/progenitor cells
File(s)Bengoa and Kypta CMLS pre-version.pdf (1.56 MB)
Accepted version
Author(s)
Bengoa-Vergniory, N
Kypta, RM
Type
Journal Article
Abstract
The first mammalian Wnt to be discovered,
Wnt-1, was found to be essential for the development of a
large part of the mouse brain over 25 years ago. We have
since learned that Wnt family secreted glycolipoproteins,
of which there are nineteen, which activate a diverse network
of signals that are particularly important during
embryonic development and tissue regeneration. Wnt signals
in the developing and adult brain can drive neural stem
cell self-renewal, expansion, asymmetric cell division,
maturation and differentiation. The molecular events taking
place after a Wnt binds to its cell-surface receptors are
complex and, at times, controversial. A deeper understanding
of these events is anticipated to lead to improvements in
the treatment of neurodegenerative diseases and stem cellbased
replacement therapies. Here, we review the roles
played by Wnts in neural stem cells in the developing
mouse brain, at neurogenic sites of the adult mouse and in
neural stem cell culture models.
Wnt-1, was found to be essential for the development of a
large part of the mouse brain over 25 years ago. We have
since learned that Wnt family secreted glycolipoproteins,
of which there are nineteen, which activate a diverse network
of signals that are particularly important during
embryonic development and tissue regeneration. Wnt signals
in the developing and adult brain can drive neural stem
cell self-renewal, expansion, asymmetric cell division,
maturation and differentiation. The molecular events taking
place after a Wnt binds to its cell-surface receptors are
complex and, at times, controversial. A deeper understanding
of these events is anticipated to lead to improvements in
the treatment of neurodegenerative diseases and stem cellbased
replacement therapies. Here, we review the roles
played by Wnts in neural stem cells in the developing
mouse brain, at neurogenic sites of the adult mouse and in
neural stem cell culture models.
Date Issued
2015-08-26
Date Acceptance
2015-08-18
Citation
Cellular and Molecular Life Sciences, 2015, 72 (21), pp.4157-4172
ISSN
1420-682X
Publisher
Springer Verlag (Germany)
Start Page
4157
End Page
4172
Journal / Book Title
Cellular and Molecular Life Sciences
Volume
72
Issue
21
Copyright Statement
The final publication is available at Springer via https://dx.doi.org/10.1007/s00018-015-2028-6
Subjects
Science & Technology
Life Sciences & Biomedicine
Biochemistry & Molecular Biology
Cell Biology
Wnt signaling
Neural stem cells
Beta-catenin
AP-1 family transcription factors
EMBRYONIC STEM-CELLS
ADULT HIPPOCAMPAL NEUROGENESIS
REGULATES NEURONAL DIFFERENTIATION
CENTRAL-NERVOUS-SYSTEM
WNT/BETA-CATENIN
BETA-CATENIN
PARKINSONS-DISEASE
SELF-RENEWAL
SYNAPTIC DIFFERENTIATION
INTERMEDIATE PROGENITORS
Publication Status
Published