This study investigates the effects of a blend of Hericium erinaceus (lion's mane mushroom) extract on the differentiation of SH-SY5Y cells, a human neuroblastoma cell line, revealing potential therapeutic implications for neuroblastoma management. Treatment with this blend induced cells differentiation towards a neuron-like profile, as evidenced by enhanced neuronal excitability and upregulation of neuronal markers, such as βIII-tubulin and synaptotagmin. Additionally, the treatment significantly reduced PCNA, a key regulator of proliferation, alongside a decrease in stemness markers, indicating a shift toward a more mature and less proliferative phenotype. These findings demonstrate the ability of Hericium erinaceus to promote neuronal differentiation and inhibit proliferation in neuroblastoma cells, highlighting its therapeutic potential for managing neuroblastoma and potentially other neurological disorders. The results suggest that Hericium erinaceus may serve as a promising candidate for the development of novel neuroregenerative therapies.

Hericium erinaceus extracts promote neuronal differentiation and excitability through nootropic metabolite activity

Brandalise, Federico
Membro del Collaboration Group
;
Priori, Erica Cecilia
Membro del Collaboration Group
;
Giammello, Francesca
Membro del Collaboration Group
;
Ratto, Daniela
Membro del Collaboration Group
;
Goppa, Lorenzo
Membro del Collaboration Group
;
Locatelli, Carlo Alessandro
Membro del Collaboration Group
;
Savino, Elena
Membro del Collaboration Group
;
Roda, Elisa
Membro del Collaboration Group
;
Rossi, Paola
Membro del Collaboration Group
2025-01-01

Abstract

This study investigates the effects of a blend of Hericium erinaceus (lion's mane mushroom) extract on the differentiation of SH-SY5Y cells, a human neuroblastoma cell line, revealing potential therapeutic implications for neuroblastoma management. Treatment with this blend induced cells differentiation towards a neuron-like profile, as evidenced by enhanced neuronal excitability and upregulation of neuronal markers, such as βIII-tubulin and synaptotagmin. Additionally, the treatment significantly reduced PCNA, a key regulator of proliferation, alongside a decrease in stemness markers, indicating a shift toward a more mature and less proliferative phenotype. These findings demonstrate the ability of Hericium erinaceus to promote neuronal differentiation and inhibit proliferation in neuroblastoma cells, highlighting its therapeutic potential for managing neuroblastoma and potentially other neurological disorders. The results suggest that Hericium erinaceus may serve as a promising candidate for the development of novel neuroregenerative therapies.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1527715
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