| Literature DB >> 33129690 |
Antony Cougnoux1, Julia C Yerger1, Mason Fellmeth1, Jenny Serra-Vinardell2, Christopher A Wassif1, Niamh X Cawley1, Forbes D Porter3.
Abstract
Niemann-Pick type C1 (NPC1) is a rare neurodegenerative disease. In NPC1 mouse cerebella, the antibacterial enzyme, lysozyme (Lyz2), is significantly increased in multiple cell types. Due to its possible role in toxic fibril deposition, we confirmed Lyz2 overexpression in culture in different control and NPC1 cell types including human NPC1 fibroblasts. Lyz2 expression is induced by Toll-like receptors potentially in response to lipid storage but does not play a functional role in NPC disease pathology. Published by Elsevier Inc.Entities:
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Year: 2020 PMID: 33129690 PMCID: PMC7736542 DOI: 10.1016/j.ymgme.2020.10.009
Source DB: PubMed Journal: Mol Genet Metab ISSN: 1096-7192 Impact factor: 4.797