Low-density-lipoprotein-receptor-related protein 1 mediates Notch pathway activation.
DLL3
LRP1
Notch pathway
interaction network
leukemia
Journal
Developmental cell
ISSN: 1878-1551
Titre abrégé: Dev Cell
Pays: United States
ID NLM: 101120028
Informations de publication
Date de publication:
25 10 2021
25 10 2021
Historique:
received:
09
02
2021
revised:
18
08
2021
accepted:
14
09
2021
pubmed:
10
10
2021
medline:
16
12
2021
entrez:
9
10
2021
Statut:
ppublish
Résumé
The Notch signaling pathway controls cell growth, differentiation, and fate decisions, and its dysregulation has been linked to various human genetic disorders and cancers. To comprehensively understand the global organization of the Notch pathway and identify potential drug targets for Notch-related diseases, we established a protein interaction landscape for the human Notch pathway. By combining and analyzing genetic and phenotypic data with bioinformatics analysis, we greatly expanded this pathway and identified many key regulators, including low-density-lipoprotein-receptor-related protein 1 (LRP1). We demonstrated that LRP1 mediates the ubiquitination chain linkage switching of Delta ligands, which further affects ligand recycling, membrane localization, and stability. LRP1 inhibition led to Notch signaling inhibition and decreased tumorigenesis in leukemia models. Our study provides a glimpse into the Notch pathway interaction network and uncovers LRP1 as one critical regulator of the Notch pathway, as well as a possible therapeutic target for Notch-related cancers.
Identifiants
pubmed: 34626540
pii: S1534-5807(21)00733-4
doi: 10.1016/j.devcel.2021.09.015
pii:
doi:
Substances chimiques
Ligands
0
Lipoproteins
0
Low Density Lipoprotein Receptor-Related Protein-1
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
2902-2919.e8Informations de copyright
Copyright © 2021 The Authors. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of interests The authors declare no competing interests.