Apolipoprotein D-mediated preservation of lysosomal function promotes cell survival and delays motor impairment in Niemann-Pick type A disease

Apolipoprotein D-mediated preservation of lysosomal function promotes cell survival and delays motor impairment in Niemann-Pick type A disease

Lysosomal Storage Diseases (LSD) are genetic diseases causing systemic and nervous system dysfunction. The glia-derived lipid binding protein Apolipoprotein D (ApoD) is required for lysosomal functional integrity in glial and neuronal cells, ensuring cell survival upon oxidative stress or injury. He...

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Hlavní autoři: Raquel Pascua-Maestro, Miriam Corraliza-Gomez, Cristian Fadrique-Rojo, Maria D. Ledesma, Edward H. Schuchman, Diego Sanchez, Maria D. Ganfornina
Médium: Článek
Jazyk:English
Vydáno: Elsevier 2020-10-01
Edice:Neurobiology of Disease
Témata:
Lysosomal storage disorder
Neuroprotection
Lysosomal pH
Lysosome permeability
Lipocalin
Lipid binding protein
On-line přístup:http://www.sciencedirect.com/science/article/pii/S0969996120303211

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http://www.sciencedirect.com/science/article/pii/S0969996120303211

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