| Literature DB >> 30911934 |
Elena Chiricozzi1, Margherita Maggioni2, Erika di Biase2, Giulia Lunghi2, Maria Fazzari2, Nicoletta Loberto2, Maffioli Elisa3, Francesca Grassi Scalvini3, Gabriella Tedeschi3,4, Sandro Sonnino5.
Abstract
Recently, we demonstrated that the GM1 oligosaccharide, II3Neu5Ac-Gg4 (OligoGM1), administered to cultured murine Neuro2a neuroblastoma cells interacts with the NGF receptor TrkA, leading to the activation of the ERK1/2 downstream pathway and to cell differentiation. To understand how the activation of the TrkA pathway is able to trigger key biochemical signaling, we performed a proteomic analysis on Neuro2a cells treated with 50 μM OligoGM1 for 24 h. Over 3000 proteins were identified. Among these, 324 proteins were exclusively expressed in OligoGM1-treated cells. Interestingly, several proteins expressed only in OligoGM1-treated cells are involved in biochemical mechanisms with a neuroprotective potential, reflecting the GM1 neuroprotective effect. In addition, we found that the exogenous administration of OligoGM1 reduced the cellular oxidative stress in Neuro2a cells and conferred protection against MPTP neurotoxicity. These results confirm and reinforce the idea that the molecular mechanisms underlying the GM1 neurotrophic and neuroprotective effects depend on its oligosaccharide chain, suggesting the activation of a positive signaling starting at plasma membrane level.Entities:
Keywords: GM1 ganglioside; GM1 oligosaccharide chain; Neuroprotection; Plasma membrane signaling; Shotgun label-free proteomic; TrkA neurotrophin receptor
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Year: 2019 PMID: 30911934 DOI: 10.1007/s12035-019-1556-8
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590