Dataset DZNE-2025-00822

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png
Dataset: Proteomic analysis of bone-marrow derived macrophages from NPC1 KO mice

 ;

2024
PRoteomics IDEntifications Database

PRoteomics IDEntifications Database ()

Abstract: Niemann-Pick type C (NPC) disease is an inherited lysosomal storage disorder mainly driven by mutations in NPC1 gene, causing lipid accumulation within late endosomes/lysosomes, and resulting in progressive neurodegeneration. To study the effect of NPC1 deficiency on the innate immune system, we performed proteomics on bone-marrow derived macrophages (BMDMs) of NPC1 KO and WT mice. Without further treatment or activation, BMDMs of NPC1 KO mice showed alterations mainly related to cholesterol metabolism, which is in line with the intracellular cholesterol transport function of NPC1.


Contributing Institute(s):
  1. Neuroproteomics (AG Lichtenthaler)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

Click to display QR Code for this record

The record appears in these collections:
Document types > Other Resources > Datasets
Institute Collections > M DZNE > M DZNE-AG Lichtenthaler
Public records
Publications Database


Linked articles:

http://join2-wiki.gsi.de/foswiki/pub/Main/Artwork/join2_logo100x88.png Journal Article  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;  ;
Myeloid cell-specific loss of NPC1 in mice recapitulates microgliosis and neurodegeneration in patients with Niemann-Pick type C disease.
Science translational medicine 16(776), eadl4616 () [10.1126/scitranslmed.adl4616]  Download fulltext Files BibTeX | EndNote: XML, Text | RIS


 Record created 2025-07-08, last modified 2025-07-09


External link:
Download fulltext
Fulltext
Rate this document:

Rate this document:
1
2
3
 
(Not yet reviewed)