Differentiation of human adipose stem cells into neural phenotype by neuroblastoma- or olfactory ensheathing cells-conditioned medium

Olfactory ensheathing cells (OECs) are known to be capable of continuous neurogenesis throughout lifetime and are a source of multiple trophic factors important in central nervous system regeneration. B104 neuroblastoma cells are recognized to induce differentiation of neural stem cells into oligode...

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Veröffentlicht in:Journal of cellular physiology 2013-11, Vol.228 (11), p.2109-2118
Hauptverfasser: Lo Furno, Debora, Pellitteri, Rosalia, Graziano, Adriana C.E., Giuffrida, Rosario, Vancheri, Carlo, Gili, Elisa, Cardile, Venera
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container_end_page 2118
container_issue 11
container_start_page 2109
container_title Journal of cellular physiology
container_volume 228
creator Lo Furno, Debora
Pellitteri, Rosalia
Graziano, Adriana C.E.
Giuffrida, Rosario
Vancheri, Carlo
Gili, Elisa
Cardile, Venera
description Olfactory ensheathing cells (OECs) are known to be capable of continuous neurogenesis throughout lifetime and are a source of multiple trophic factors important in central nervous system regeneration. B104 neuroblastoma cells are recognized to induce differentiation of neural stem cells into oligodendrocyte precursor cells. Therefore, the aim of this study was to verify if conditioned medium (CM) obtained from OECs or B104 cells was capable of inducing differentiation of adipose tissue‐derived mesenchymal stem cells (AT‐MSCs) to a neuronal phenotype. In order to this goal, immunocytochemical procedures and flow cytometry analysis were used and some neural markers, as nestin, protein gene product 9.5 (PGP 9.5), microtubule‐associated protein 2 (MAP2), glial fibrillary acidic protein (GFAP), and neuron cell surface antigen (A2B5) were examined 24 h and 7 days after the treatment. The results showed that both OECs‐ or B104‐CM treated AT‐MSCs express markers of progenitor and mature neurons (nestin, PGP 9.5 and MAP2) in time‐dependent manner, display morphological features resembling neuronal cells, and result negative for GFAP and A2B5, astrocyte and oligodendrocyte markers, respectively. This study demonstrated that AT‐MSCs can be influenced by the environment, indicating that these cells can respond to environmental cues also versus a neuronal phenotype. J. Cell. Physiol. 228: 2109–2118, 2013. © 2013 Wiley Periodicals, Inc.
doi_str_mv 10.1002/jcp.24386
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B104 neuroblastoma cells are recognized to induce differentiation of neural stem cells into oligodendrocyte precursor cells. Therefore, the aim of this study was to verify if conditioned medium (CM) obtained from OECs or B104 cells was capable of inducing differentiation of adipose tissue‐derived mesenchymal stem cells (AT‐MSCs) to a neuronal phenotype. In order to this goal, immunocytochemical procedures and flow cytometry analysis were used and some neural markers, as nestin, protein gene product 9.5 (PGP 9.5), microtubule‐associated protein 2 (MAP2), glial fibrillary acidic protein (GFAP), and neuron cell surface antigen (A2B5) were examined 24 h and 7 days after the treatment. 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subjects Adipose tissue
Adipose Tissue - cytology
Adult
Animals
Astrocytes
Biomarkers - metabolism
Cell Differentiation - drug effects
Cell Line, Tumor
Cell Shape - drug effects
Central nervous system
Culture Media, Conditioned - pharmacology
Female
Flow Cytometry
Humans
Immunophenotyping
Male
Mesenchymal Stromal Cells - cytology
Mesenchymal Stromal Cells - drug effects
Mesenchymal Stromal Cells - metabolism
Neuroblastoma - pathology
Neurons - cytology
Neurons - drug effects
Neurons - metabolism
Olfactory Bulb - cytology
Phenotype
Rats
Stem cells
Young Adult
title Differentiation of human adipose stem cells into neural phenotype by neuroblastoma- or olfactory ensheathing cells-conditioned medium
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