Electric field-induced astrocyte alignment directs neurite outgrowth.
← Research streamRat astrocytes were pre-aligned by exposure to an electric field of physiological strength (500 mV mm(-1)). Neurite outgrowth at 24 and 48 hours was significantly enhanced and consistently directed along aligned astrocyte processes, and this directed outgrowt…
Study snapshot
Abstract
The extension and directionality of neurite outgrowth are key to achieving successful target connections during both CNS development and during the re-establishment of connections lost after neural trauma. The degree of axonal elongation depends, in large part, on the spatial arrangement of astrocytic processes rich in growth-promoting proteins. Because astrocytes in culture align their processes on exposure to an electrical field of physiological strength, we sought to determine the extent to which aligned astrocytes affect neurite outgrowth. To this end, dorsal root ganglia cells were seeded onto cultured rat astrocytes that were pre-aligned by exposure to an electric field of physiological strength (500 mV mm(-1)). Using confocal microscopy and digital image analysis, we found that neurite outgrowth at 24 hours and at 48 hours is enhanced significantly and directed consistently along the aligned astrocyte processes. Moreover, this directed neurite outgrowth is maintained when grown on fixed, aligned astrocytes. Collectively, these results indicate that endogenous electric fields present within the developing CNS might act to align astrocyte processes, which can promote and direct neurite growth. Furthermore, these results demonstrate a simple method to produce an aligned cellular substrate, which might be used to direct regenerating neurites.
AI evidence extraction
Structured fields below were generated from the paper’s abstract and metadata to make the evidence easier to inspect. Automated extraction may be incomplete or incorrect; verify important details against the original paper.
Main findings
Rat astrocytes were pre-aligned by exposure to an electric field of physiological strength (500 mV mm(-1)). Neurite outgrowth at 24 and 48 hours was significantly enhanced and consistently directed along aligned astrocyte processes, and this directed outgrowth persisted on fixed aligned astrocytes.
Outcomes measured
- Astrocyte process alignment
- Neurite outgrowth enhancement at 24 and 48 hours
- Directionality of neurite outgrowth along aligned astrocyte processes
- Maintenance of directed neurite outgrowth on fixed aligned astrocytes
Limitations
- In vitro cell culture model; findings may not directly translate to in vivo CNS development or injury repair
- No exposure duration reported in the abstract
- Sample size and statistical details not provided in the abstract
View raw extracted JSON
{
"study_type": "in_vitro",
"exposure": {
"band": null,
"source": "electric field (cell culture)",
"frequency_mhz": null,
"sar_wkg": null,
"duration": null
},
"population": "Cultured rat astrocytes with seeded dorsal root ganglia cells (in vitro)",
"sample_size": null,
"outcomes": [
"Astrocyte process alignment",
"Neurite outgrowth enhancement at 24 and 48 hours",
"Directionality of neurite outgrowth along aligned astrocyte processes",
"Maintenance of directed neurite outgrowth on fixed aligned astrocytes"
],
"main_findings": "Rat astrocytes were pre-aligned by exposure to an electric field of physiological strength (500 mV mm(-1)). Neurite outgrowth at 24 and 48 hours was significantly enhanced and consistently directed along aligned astrocyte processes, and this directed outgrowth persisted on fixed aligned astrocytes.",
"effect_direction": "benefit",
"limitations": [
"In vitro cell culture model; findings may not directly translate to in vivo CNS development or injury repair",
"No exposure duration reported in the abstract",
"Sample size and statistical details not provided in the abstract"
],
"evidence_strength": "low",
"confidence": 0.74,
"peer_reviewed_likely": "yes",
"keywords": [
"electric field",
"astrocyte alignment",
"neurite outgrowth",
"dorsal root ganglia",
"confocal microscopy",
"cell culture",
"CNS development",
"neural regeneration"
],
"suggested_hubs": []
}AI-extracted fields are generated from the abstract and metadata and may be incomplete or incorrect. This material is for informational purposes and is not medical advice.
Identifiers and source
DOI: 10.1017/s1740925x0600010x
PubMed: 18458757
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