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Moreno-Flores MT, Díaz-Nido J, Wandosell F, et al. Olfactory Ensheathing Glia: Drivers of Axonal Regeneration in the Central Nervous System?. J Biomed Biotechnol. 2002;2(1):37-43doi: 10.1155/S1110724302000372.
Moreno-Flores, M. T., Díaz-Nido, J., Wandosell, F., & Avila, J. (2002). Olfactory Ensheathing Glia: Drivers of Axonal Regeneration in the Central Nervous System?. Journal of biomedicine & biotechnology, 2(1), 37-43. https://doi.org/10.1155/S1110724302000372
Moreno-Flores, M. Teresa, et al. "Olfactory Ensheathing Glia: Drivers of Axonal Regeneration in the Central Nervous System?." Journal of biomedicine & biotechnology vol. 2,1 (2002): 37-43. doi: https://doi.org/10.1155/S1110724302000372
Moreno-Flores MT, Díaz-Nido J, Wandosell F, Avila J. Olfactory Ensheathing Glia: Drivers of Axonal Regeneration in the Central Nervous System?. J Biomed Biotechnol. 2002;2(1):37-43. doi: 10.1155/S1110724302000372. PMID: 12488598; PMCID: PMC139118.
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J Biomed Biotechnol. 2002;2(1):37-43. doi: 10.1155/S1110724302000372.

Olfactory Ensheathing Glia: Drivers of Axonal Regeneration in the Central Nervous System?.

Journal of biomedicine & biotechnology

M. Teresa Moreno-Flores, Javier Díaz-Nido, Francisco Wandosell, Jesús Avila

PMID: 12488598 PMCID: PMC139118 DOI: 10.1155/S1110724302000372

Abstract

Olfactory ensheathing glia (OEG) accompany olfactory growing axons in their entry to the adult mammalian central nervous system (CNS). Due to this special characteristic, considerable attention has been focused on the possibility of using OEG for CNS regeneration. OEG present a large heterogeneity in culture with respect to their cellular morphology and expressed molecules. The specific characteristics of OEG responsible for their regenerative properties have to be defined. These properties probably result from the combination of several factors: molecular composition of the membrane (expressing adhesion molecules as PSA-NCAM, L1 and/or others) combined with their ability to reduce glial scarring and to accompany new growing axons into the host CNS. Their capacity to produce some neurotrophic factors might also account for their ability to produce CNS regeneration.

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