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Status |
Public on Jul 22, 2015 |
Title |
Robust axonal regeneration occurs in the injured CAST/Ei mouse central nervous system |
Organism |
Mus musculus |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Axon regeneration in the central nervous system (CNS) requires reactivating injured neurons’ intrinsic growth state and enabling growth in an inhibitory environment. Using an inbred mouse neuronal phenotypic screen, we find that CAST/Ei mouse adult dorsal root ganglion neurons extend axons more on CNS myelin than the other eight strains tested, especially when pre-injured. Injury-primed CAST/Ei neurons also regenerate markedly in the spinal cord and optic nerve more than those from C57BL/6 mice and show greater spouting following ischemic stroke. Heritability estimates indicate that extended growth in CAST/Ei neurons on myelin is genetically determined, and two whole-genome expression screens yield the Activin transcript Inhba as most correlated with this ability. These screens are presented here.
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Overall design |
Biological quadruplicate - Mouse tissue - Naïve Dorsal Root Ganglia (DRG) and 5 day post sciatic nerve crush DRG - x9 strains.
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Contributor(s) |
Costigan M, Coppola G |
Citation(s) |
26004914 |
Submission date |
Mar 20, 2015 |
Last update date |
May 15, 2019 |
Contact name |
Giovanni Coppola |
E-mail(s) |
gcoppola@ucla.edu
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Phone |
310-794-4172
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Organization name |
UCLA
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Department |
Psychiatry and Neurology
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Lab |
Neurogenetics
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Street address |
1524 Gonda, 695 Charles Young Drive South
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City |
Los Angeles |
State/province |
CA |
ZIP/Postal code |
90095 |
Country |
USA |
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Platforms (1) |
GPL9185 |
Illumina Genome Analyzer (Mus musculus) |
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Samples (24)
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Relations |
BioProject |
PRJNA279017 |
SRA |
SRP056393 |