Induction of epidermis and inhibition of neural fate by Bmp-4
Abstract
During gastrulation in vertebrates, ectodermal cells choose between two fates, neural and epidermal. The nervous system forms in response to signals from the Spemann organizer; ectoderm that does not receive these signals becomes epidermis. Unexpectedly, however, in Xenopus, neural tissue also forms when cell-cell communication within the ectoderm is disrupted by cell dissociation or by antagonists of the growth factor activin. These observations suggest that epidermal specification depends on local signalling, by activin or a close relative, and that neural tissue forms when this communication is blocked. Here we report that bone morphogenesis protein 4 (Bmp-4), a relative of activin that is expressed in the embryo at the time of ectodermal fate determination, is a potent epidermal inducer and neural inhibitor, the first reported in any vertebrate. Activin can inhibit neuralization by inducing mesoderm, but does not induce epidermis. Moreover, the dominant-negative activin receptor, which stimulates neuralization when expressed in the embryo, blocks Bmp-4 in our assay. Our findings demonstrate that epidermal fate can be induced, and thus provide further evidence that neural specification is under inhibitory control in vertebrates.
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TGFβ inhibition promotes ectoderm induction from pluripotent stem cells.
“TGFβ inhibition promotes ectoderm induction from pluripotent stem cells, whereas BMP activation promotes surface ectoderm (alternatively, non-neural ectoderm) induction and suppresses neuroectoderm induction9–12.”
From Hair-bearing human skin generated entirely from pluripotent stem cells (2020) · cites this paper as [12]
BMP activation promotes surface ectoderm induction and suppresses neuroectoderm induction.
“TGFβ inhibition promotes ectoderm induction from pluripotent stem cells, whereas BMP activation promotes surface ectoderm (alternatively, non-neural ectoderm) induction and suppresses neuroectoderm induction9–12.”
From Hair-bearing human skin generated entirely from pluripotent stem cells (2020) · cites this paper as [12]
To successfully generate skin, co-development of epidermis and dermis is required, and precise alterations of major signaling pathways (TGF-β, BMP4, and bFGF) are critical.
“To successfully generate skin, co-development of epidermis and dermis is required, and precise alterations of major signaling pathways (TGF-β, BMP4, and bFGF) are critical”
From Generation and characterization of hair-bearing skin organoids from human pluripotent stem cells (2022) · cites this paper as [36]
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References 28 · Cited by 787
- Authors
- Wilson, P. A., & Hemmati-Brivanlou, A.
- Affiliations
- Rockefeller University (US)
- ORCID
- Wilson, Paul A.
- Venue
- Nature
- Published
- 1995-07
- Volume
- 376
- Issue
- 6538
- Pages
- 331-333
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2092911887
- Cited by
- 787
- References
- 28
- Citations by year
- 2026: 6 · 2025: 8 · 2024: 17 · 2023: 19 · 2022: 15 · 2021: 12 · 2020: 18 · 2019: 14 · 2018: 14 · 2017: 15 · 2016: 19 · 2015: 13 · 2014: 20 · 2013: 22 · 2012: 32
- FWCI
- 19.82
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Keywords
- BMP4, neural fate specification, activin, Spemann organizer, cell-to-cell communication, Xenopus gastrulation, mesoderm induction
- MeSH terms
- Animals, Base Sequence, Ectoderm, Embryonic Induction, Epidermis, Gastrula, Glycoproteins, Growth Substances, Humans, Inhibins, Molecular Sequence Data, Neurons, Oligodeoxyribonucleotides, Proteins, Xenopus, Receptors, Growth Factor, Bone Morphogenetic Proteins, Activins, Activin Receptors, Follistatin, Culture Techniques
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