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Viability of olfactory ensheathing cells after hypoxia and serum deprivation: Implication for therapeutic transplantation
Author(s) -
Pellitteri Rosalia,
Catania Maria Vincenza,
Bonaccorso Carmela Maria,
Ranno Eugenia,
Dell'Albani Paola,
Zaccheo Damiano
Publication year - 2014
Publication title -
journal of neuroscience research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.72
H-Index - 160
eISSN - 1097-4547
pISSN - 0360-4012
DOI - 10.1002/jnr.23442
Subject(s) - olfactory ensheathing glia , transplantation , neurotrophic factors , glial cell line derived neurotrophic factor , biology , remyelination , ciliary neurotrophic factor , microbiology and biotechnology , viability assay , growth factor , immunology , neuroscience , cell , medicine , myelin , central nervous system , olfactory bulb , biochemistry , receptor
Olfactory ensheathing cells (OECs) represent glial cells supporting neuronal turnover in the olfactory system. In vitro, OECs promote axonal growth as a source of neurotrophic growth factors; in vivo, they produce myelin, promoting remyelination of damaged axons. Consequently, OEC transplantation appears to be a promising treatment for spinal cord injury, although the functional recovery is limited. This might be ascribed to the microenvironment at the lesion site, lacking growth factors (GFs), nutrients, and oxygen. To mimic this condition, we used an in vitro approach by growing primary neonatal mouse OECs under hypoxic conditions and/or serum deprivation. In addition, we compared OECs survival/proliferation with that of primary cultures of Schwann cells (SCs) and astrocytes under the same experimental conditions. Cultures were analyzed by immunocytochemistry, and cell viability was evaluated by MTT assay. Different GFs, such as NGF, bFGF, and GDNF, and their combination were used to rescue cells from serum and/or oxygen deprivation. We show that the cell types were differently sensitive to the tested stress conditions and that OECs were the most sensitive among them. Moreover, OEC viability was rescued by bFGF under serum‐deprived or hypoxic condition but not under conditions of drastic serum deprivation and hypoxia. bFGF was effective also for the other cell types, whereas the effect of the other GFs was negligible. This model suggests that administration of bFGF might be considered useful to sustain cell survival/proliferation after transplantation of OECs either alone or in combination with other glial cell types. © 2014 Wiley Periodicals, Inc.