The DOI matches its Crossref record; 56 of the 57 references it cites were found in a registry or an index.
TGF-β Signaling Specifies Axons during Brain Development
Open accessAbstract
In the mammalian brain, the specification of a single axon and multiple dendrites occurs early in the differentiation of most neuron types. Numerous intracellular signaling events for axon specification have been described in detail. However, the identity of the extracellular factor(s) that initiate neuronal polarity in vivo is unknown. Here, we report that transforming growth factor beta (TGF-beta) initiates signaling pathways both in vivo and in vitro to fate naive neurites into axons. Neocortical neurons lacking the type II TGF-beta receptor (TbetaR2) fail to initiate axons during development. Exogenous TGF-beta is sufficient to direct the rapid growth and differentiation of an axon, and genetic enhancement of receptor activity promotes the formation of multiple axons. Finally, we show that the bulk of these TGF-beta-dependent events are mediated by site-specific phosphorylation of Par6. These results define an extrinsic cue for neuronal polarity in vivo that patterns neural circuits in the developing brain.
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“These growth factors may produce non-canonical signaling outside of the Smad transcription factors, such as through the MAPK pathway40,41.”
From GDF10 is a signal for axonal sprouting and functional recovery after stroke (2015) · cites this paper as [40]
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“In other in vitro systems, TGFβ promotes axonal outgrowth of injured neurons21,22,39,40 and blockade of TGFβRII alters neuronal polarity and leads to shorter axons42.”
From GDF10 is a signal for axonal sprouting and functional recovery after stroke (2015) · cites this paper as [40]
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Citations
Cites
Mechanisms of TGF-β Signaling from Cell Membrane to the Nucleus
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The establishment of polarity by hippocampal neurons in culture.
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TGF-β and epithelial-to-mesenchymal transitions
Zavadil, J., & Böttinger, E. P. (2005) · Oncogene · doi:10.1038/sj.onc.1208927 · Cited by 1,628
TGFβ signals through a heteromeric protein kinase receptor complex
Wrana, J. L., Attisano, L., Cárcamo, J. M., Zentella‐Dehesa, A., Doody, J. F., Laiho, M., Wang, X.-F., & Massagué, J. (1992) · Cell · doi:10.1016/0092-8674(92)90395-s · Cited by 1,528
Autocrine Secretion and Malignant Transformation of Cells
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Reinsertion or Degradation of AMPA Receptors Determined by Activity-Dependent Endocytic Sorting
Ehlers, M. D. (2000) · Neuron · doi:10.1016/s0896-6273(00)00129-x · Cited by 1,096
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1 of the 57 references couldn’t be matched to a known paper.
Research works printed but not linked: 1
- Hand, R., Bortone, D., Mattar, P., Nguyen, L., Heng, J.I., Guerrier, S., Boutt, E., Peters, E., Barnes, A.P., Parras, C., et al. (2005). Neuron 48, 45–62. · DOI
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Sorted by citations
Massagué, J. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3434 · Cited by 3,239
Transforming Growth Factor-β Signaling in Immunity and Cancer
Batlle, E., & Massagué, J. (2019) · Immunity · doi:10.1016/j.immuni.2019.03.024 · Cited by 2,366
TGF-β and BMP Signaling in Osteoblast Differentiation and Bone Formation
Chen, G., Deng, C., & Li, Y.-P. (2012) · International Journal of Biological Sciences · doi:10.7150/ijbs.2929 · Cited by 1,756
TGF-β signaling in health, disease and therapeutics
Deng, Z., Fan, T. T., Chu, X., Tian, H., Zheng, Y., Li, C., & He, J. (2024) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-024-01764-w · Cited by 1,360
A Review of the Clinical Side Effects of Bone Morphogenetic Protein-2
James, A. W., LaChaud, G., Shen, J., Asatrian, G., Nguyen, V., Zhang, X., Ting, K., & Soo, C. (2016) · Tissue Engineering Part B: Reviews · doi:10.1089/ten.teb.2015.0357 · Cited by 1,131
Metadata
- Authors
- Yi, J. J., Barnes, A. P., Hand, R., Polleux, F., & Ehlers, M. D.
- Affiliations
- Duke Medical Center (US)
- University of North Carolina at Chapel Hill (US)
- Howard Hughes Medical Institute (US)
- Corresponding author
- Ehlers, Michael D.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2010-07
- Volume
- 142
- Issue
- 1
- Pages
- 144-157
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC2933408
- OpenAlex
- W1991732233
- Cited by
- 284
- References
- 57
- Citations by year
- 2026: 12 · 2025: 5 · 2024: 10 · 2023: 15 · 2022: 18 · 2021: 30 · 2020: 26 · 2019: 15 · 2018: 11 · 2017: 16 · 2016: 13 · 2015: 20 · 2014: 15 · 2013: 24 · 2012: 28
- FWCI
- 9.51
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- Howard Hughes Medical Institute
- National Institute of Mental Health (K01MH080259)
- National Institute of Neurological Disorders and Stroke (R01NS047574)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Axon Guidance and Neuronal Signaling
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- TGF-beta signaling, axon specification, neuronal polarity, dendrite formation, TGFBR2, neocortical neurons, axon growth, neural circuit development
- MeSH terms
- Receptor, Transforming Growth Factor-beta Type II, Animals, Axons, Embryo, Mammalian, Neurons, Phosphorylation, Signal Transduction, Transforming Growth Factor beta, Protein Serine-Threonine Kinases, Receptors, Transforming Growth Factor beta, Neocortex, Adaptor Proteins, Signal Transducing, Mice
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