Role of lipid rafts in neuronal differentiation of dental pulp-derived stem cells

Human dental pulp-derived stem cells (hDPSCs) are characterized by a typical fibroblast-like morphology. They express specific markers for mesenchymal stem cells and are capable of differentiation into osteoblasts, adipoblasts and neurons in vitro. Previous studies showed that gangliosides are invol...

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Veröffentlicht in:Experimental cell research 2015-12, Vol.339 (2), p.231-240
Hauptverfasser: Mattei, Vincenzo, Santacroce, Costantino, Tasciotti, Vincenzo, Martellucci, Stefano, Santilli, Francesca, Manganelli, Valeria, Piccoli, Luca, Misasi, Roberta, Sorice, Maurizio, Garofalo, Tina
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Sprache:eng
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Zusammenfassung:Human dental pulp-derived stem cells (hDPSCs) are characterized by a typical fibroblast-like morphology. They express specific markers for mesenchymal stem cells and are capable of differentiation into osteoblasts, adipoblasts and neurons in vitro. Previous studies showed that gangliosides are involved in the induction of early neuronal differentiation of hDPSCs. This study was undertaken to investigate the role of lipid rafts in this process. Lipid rafts are signaling microdomains enriched in glycosphingolipids, cholesterol, tyrosine kinase receptors, mono- or heterotrimeric G proteins and GPI-anchored proteins. We preliminary showed that established cells expressed multipotent mesenchymal stromal-specific surface antigens. Then, we analyzed the distribution of lipid rafts, revealing plasma membrane microdomains with GM2 and EGF-R enrichment. Following stimulation with EGF/bFGF, neuronal differentiation was observed. To analyze the functional role of lipid rafts in EGF/bFGF-induced hDPSCs differentiation, cells were preincubated with lipid raft affecting agents, i.e. [D]-PDMP or methyl-β-cyclodextrin. These compounds significantly prevented neuronal-specific antigen expression, as well as Akt and ERK 1/2 phosphorylation, induced by EGF/bFGF, indicating that lipid raft integrity is essential for EGF/bFGF-induced hDPSCs differentiation. These results suggest that lipid rafts may represent specific chambers, where multimolecular signaling complexes, including lipids (gangliosides, cholesterol) and proteins (EGF-R), play a role in hDPSCs differentiation. •We analyzed the role of lipid rafts during neuronal differentiation of hDPSCs.•Plasma membrane lipid rafts with GM2 and EGF-R enrichment were detected.•Following stimulation with EGF/bFGF, neuronal differentiation of hDPSCs was observed.•Akt and ERK phosphorylations were prevented by [D]-PDMP or methyl-β-cyclodextrin.•Rafts represent specific “chambers” which play a role in hDPSCs differentiation.
ISSN:0014-4827
1090-2422
DOI:10.1016/j.yexcr.2015.11.012