A local Wnt-3a signal is required for development of the mammalian hippocampus
pmid: 10631167
A local Wnt-3a signal is required for development of the mammalian hippocampus
ABSTRACT The mechanisms that regulate patterning and growth of the developing cerebral cortex remain unclear. Suggesting a role for Wnt signaling in these processes, multiple Wnt genes are expressed in selective patterns in the embryonic cortex. We have examined the role of Wnt-3a signaling at the caudomedial margin of the developing cerebral cortex, the site of hippocampal development. We show that Wnt-3a acts locally to regulate the expansion of the caudomedial cortex, from which the hippocampus develops. In mice lacking Wnt-3a, caudomedial cortical progenitor cells appear to be specified normally, but then underproliferate. By mid-gestation, the hippocampus is missing or represented by tiny populations of residual hippocampal cells. Thus, Wnt-3a signaling is crucial for the normal growth of the hippocampus. We suggest that the coordination of growth with patterning may be a general role for Wnts during vertebrate development.
- University of Chicago United States
- Harvard University United States
Cerebral Cortex, Mammals, Mice, Knockout, Neurons, Telencephalon, Stem Cells, Gene Expression Regulation, Developmental, Proteins, Gestational Age, Hippocampus, Wnt Proteins, Wnt3 Protein, Embryonic and Fetal Development, Mice, Wnt3A Protein, Animals, Signal Transduction
Cerebral Cortex, Mammals, Mice, Knockout, Neurons, Telencephalon, Stem Cells, Gene Expression Regulation, Developmental, Proteins, Gestational Age, Hippocampus, Wnt Proteins, Wnt3 Protein, Embryonic and Fetal Development, Mice, Wnt3A Protein, Animals, Signal Transduction
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