The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Small Proline-Rich Repeat Protein 1A Is Expressed by Axotomized Neurons and Promotes Axonal Outgrowth
Open accessAbstract
The ability of neurons to regenerate an axon after injury is determined by both the surrounding environment and factors intrinsic to the damaged neuron. We have used cDNA microarrays to survey those genes induced during successful sciatic nerve regeneration. The small proline-rich repeat protein 1A (SPRR1A) is not detectable in uninjured neurons but is induced by >60-fold after peripheral axonal damage. The protein is localized to injured neurons and axons. sprr1a is one of a group of epithelial differentiation genes, including s100c and p21/waf, that are coinduced in neurons by axotomy. Overexpressed SPRR1A colocalizes with F-actin in membrane ruffles and augments axonal outgrowth on a range of substrates. In axotomized sensory neurons, reduction of SPRR1A function restricts axonal outgrowth. Neuronal SPRR1A may be a significant contributor to successful nerve regeneration.
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Cites
Stoll, G., Griffin, J. W., Li, C. Y., & Trapp, B. D. (1989) · Journal of Neurocytology · doi:10.1007/bf01187086 · Cited by 556
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Cellular and molecular mechanisms of neural repair after stroke: making waves
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“, 2007) in neurons Promotes neurite outgrowth (Bonilla et al., 2002)”
Background
Metadata
- Authors
- Bonilla, I. E., Tanabe, K., & Strittmatter, S. M.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2002-02-15
- Volume
- 22
- Issue
- 4
- Pages
- 1303-1315
- ISSN
- 0270-6474 (ISSN-L)
- 1529-2401
- OpenAlex
- W1866441697
- Cited by
- 296
- References
- 1
- FWCI
- 4.97
- Type
- journal article
- Language
- en
- Open access
- bronze
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.
