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Developmental Biology
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Developmental Biology
Article . 2005
License: Elsevier Non-Commercial
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Fgfr1-dependent boundary cells between developing mid- and hindbrain

Authors: Trokovic, R.; Jukkola, T.; Saarimaki, J.; Peltopuro, P.; Naserke, T.; Weisenhorn, D.M.; Trokovic, N.; +2 Authors

Fgfr1-dependent boundary cells between developing mid- and hindbrain

Abstract

Signaling molecules regulating development of the midbrain and anterior hindbrain are expressed in distinct bands of cells around the midbrain-hindbrain boundary. Very little is known about the mechanisms responsible for the coherence of this signaling center. One of the fibroblast growth factor (FGF) receptors, Fgfr1, is required for establishment of a straight border between developing mid- and hindbrain. Here we show that the cells close to the border have unique features. Unlike the cells further away, these cells express Fgfr1 but not the other FGF receptors. The cells next to the midbrain-hindbrain boundary express distinct cell cycle regulators and proliferate less rapidly than the surrounding cells. In Fgfr1 mutants, these cells fail to form a coherent band at the boundary. The slowly proliferating boundary cells are necessary for development of the characteristic isthmic constriction. They may also contribute to compartmentalization of this brain region.

Country
Germany
Keywords

Male, Proliferation, Embryonic Development, Development, Midbrain, Mice, Mesencephalon, Cerebellum, Rhombomere, In Situ Nick-End Labeling, Morphogenesis, FGF, Animals, RNA, Messenger, Receptor, Fibroblast Growth Factor, Type 1, Molecular Biology, Alleles, Crosses, Genetic, In Situ Hybridization, Mice, Inbred ICR, Isthmic organizer, Cell adhesion, Gene Expression Regulation, Developmental, Receptor Protein-Tyrosine Kinases, Cell Biology, Receptors, Fibroblast Growth Factor, Cyclin, Mice, Mutant Strains, Rhombencephalon, Female, Developmental Biology

  • BIP!
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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    65
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
65
Top 10%
Top 10%
Top 10%
hybrid