BMP signalling inhibits premature neural differentiation in the mouse embryo
BMP signalling inhibits premature neural differentiation in the mouse embryo
The specification of a subset of epiblast cells to acquire a neural fate constitutes the first step in the generation of the nervous system. Little is known about the signals required for neural induction in the mouse. We have analysed the role of BMP signalling in this process. We demonstrate that prior to gastrulation, Bmp2/4 signalling via Bmpr1a maintains epiblast pluripotency and prevents precocious neural differentiation of this tissue, at least in part by maintaining Nodal signalling. We find that during gastrulation, BMPs of the 60A subgroup cooperate with Bmp2/4 to maintain pluripotency. The inhibition of neural fate by BMPs is independent of FGF signalling, as inhibition of FGF signalling between 5.5 and 7.5 days post-coitum does not block neural differentiation in the mouse embryo. Together, our results demonstrate that inhibition of BMP signalling has a central role during neural induction in mammals and suggest that FGFs do not act as neural inducers in the post-implantation mouse embryo.
- National Institute of Health Pakistan
- University of Bristol United Kingdom
- Imperial College London United Kingdom
- MRC London Institute of Medical Sciences United Kingdom
- National Institutes of Health United States
Pluripotent Stem Cells, 570, Bone Morphogenetic Protein 7, 610, Bone Morphogenetic Protein 2, Embryonic Development, Cell Differentiation, Bone Morphogenetic Protein 4, Embryo, Mammalian, Nervous System, Mice, Mutant Strains, Fibroblast Growth Factors, Mice, Transforming Growth Factor beta, Bone Morphogenetic Proteins, Animals, Bone Morphogenetic Protein Receptors, Type I, Signal Transduction
Pluripotent Stem Cells, 570, Bone Morphogenetic Protein 7, 610, Bone Morphogenetic Protein 2, Embryonic Development, Cell Differentiation, Bone Morphogenetic Protein 4, Embryo, Mammalian, Nervous System, Mice, Mutant Strains, Fibroblast Growth Factors, Mice, Transforming Growth Factor beta, Bone Morphogenetic Proteins, Animals, Bone Morphogenetic Protein Receptors, Type I, Signal Transduction
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