Naringenin and SMER28 target lysosomal reformation and rescue SPG11 and SPG15 hereditary spastic paraplegia phenotypes

SPG11 and SPG15 are two hereditary spastic paraplegia forms characterized by autophagosome accumulation, reduced free lysosomes and defects in autophagic lysosomal reformation (ALR). We demonstrated that attempts to rescue ALR and/or lysosome biogenesis are critical strategies for SPG15 phenotype an...

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Bibliografski detalji

Glavni autori:	Chiara Vantaggiato, Giulia Guarato, Francesca Brivio, Elena Panzeri, Beatrice Speltoni, Sentiljana Gumeni, Genny Orso, Filippo Maria Santorelli, Maria Teresa Bassi
Format:	Artigo
Jezik:	Inglês
Izdano:	Elsevier 2025-08-01
Serija:	Pharmacological Research
Teme:	Naringenin Tideglusib SMER28 ALR Lysosomes SPG15
Online pristup:	http://www.sciencedirect.com/science/article/pii/S1043661825002610
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