A top-down approach to uncover the hidden ligandome of low-density lipoprotein receptor-related protein 1 in cartilage.


Journal

Matrix biology : journal of the International Society for Matrix Biology
ISSN: 1569-1802
Titre abrégé: Matrix Biol
Pays: Netherlands
ID NLM: 9432592

Informations de publication

Date de publication:
09 2022
Historique:
received: 11 03 2022
revised: 26 07 2022
accepted: 17 08 2022
pubmed: 27 8 2022
medline: 4 10 2022
entrez: 26 8 2022
Statut: ppublish

Résumé

The low-density lipoprotein receptor-related protein 1 (LRP1) is a cell-surface receptor ubiquitously expressed in various tissues. It plays tissue-specific roles by mediating endocytosis of a diverse range of extracellular molecules. Dysregulation of LRP1 is involved in multiple conditions including osteoarthritis (OA) but little information is available about the specific profile of direct binding partners of LRP1 (ligandome) for each tissue, which would lead to a better understanding of its role in disease states. Here, we investigated adult articular cartilage where impaired LRP1-mediated endocytosis leads to tissue destruction. We used a top-down approach involving proteomic analysis of the LRP1 interactome in human chondrocytes, direct binding assays using purified LRP1 and ligand candidates, and validation in LRP1-deficient fibroblasts and human chondrocytes, as well as a novel Lrp1 conditional knockout (KO) mouse model. We found that inhibition of LRP1 and ligand interaction results in cell death, alteration of the entire secretome and transcriptional modulations in human chondrocytes. We identified a chondrocyte-specific LRP1 ligandome consisting of more than 50 novel ligand candidates. Surprisingly, 23 previously reported LRP1 ligands were not regulated by LRP1-mediated endocytosis in human chondrocytes. We confirmed direct LRP1 binding of HGFAC, HMGB1, HMGB2, CEMIP, SLIT2, ADAMTS1, TSG6, IGFBP7, SPARC and LIF, correlation between their affinity for LRP1 and the rate of endocytosis, and some of their intracellular localization. Moreover, a conditional LRP1 KO mouse model demonstrated a critical role of LRP1 in regulating the high-affinity ligands in cartilage in vivo. This systematic approach revealed the specificity and the extent of the chondrocyte LRP1 ligandome and identified potential novel therapeutic targets for OA.

Identifiants

pubmed: 36028175
pii: S0945-053X(22)00101-9
doi: 10.1016/j.matbio.2022.08.007
pii:
doi:

Substances chimiques

HMGB1 Protein 0
HMGB2 Protein 0
LRP1 protein, human 0
Ligands 0
Lipoproteins, LDL 0
Low Density Lipoprotein Receptor-Related Protein-1 0
Lrp1 protein, mouse 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

190-218

Subventions

Organisme : British Heart Foundation
ID : FS/IBSRF/20/25032
Pays : United Kingdom
Organisme : Versus Arthritis
ID : 21447
Pays : United Kingdom

Informations de copyright

Crown Copyright © 2022. Published by Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that there are no conflicts of interests.

Auteurs

Kazuhiro Yamamoto (K)

Institute of Life Course and Medical Sciences, William Henry Duncan Building, University of Liverpool, 6 West Derby Street, Liverpool L7 8TX, United Kingdom. Electronic address: Kazuhiro.yamamoto@liverpool.ac.uk.

Carsten Scavenius (C)

Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark.

Maria M Meschis (MM)

Institute of Life Course and Medical Sciences, William Henry Duncan Building, University of Liverpool, 6 West Derby Street, Liverpool L7 8TX, United Kingdom.

Abdulrahman M E Gremida (AME)

Institute of Life Course and Medical Sciences, William Henry Duncan Building, University of Liverpool, 6 West Derby Street, Liverpool L7 8TX, United Kingdom.

Emilie H Mogensen (EH)

Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark.

Ida B Thøgersen (IB)

Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark.

Simone Bonelli (S)

Fondazione RiMED - ISMETT via Ernesto Tricomi 5, Palermo 90127, Italy.

Simone D Scilabra (SD)

Fondazione RiMED - ISMETT via Ernesto Tricomi 5, Palermo 90127, Italy.

Anders Jensen (A)

Institute of Life Course and Medical Sciences, William Henry Duncan Building, University of Liverpool, 6 West Derby Street, Liverpool L7 8TX, United Kingdom.

Salvatore Santamaria (S)

Department of Immunology and Inflammation, Imperial College London, Du Cane Road, , London W12 0NN, United Kingdom.

Josefin Ahnström (J)

Department of Immunology and Inflammation, Imperial College London, Du Cane Road, , London W12 0NN, United Kingdom.

George Bou-Gharios (G)

Institute of Life Course and Medical Sciences, William Henry Duncan Building, University of Liverpool, 6 West Derby Street, Liverpool L7 8TX, United Kingdom.

Jan J Enghild (JJ)

Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark.

Hideaki Nagase (H)

Kennedy Institute of Rheumatology, University of Oxford, Headington, Oxford OX3 7FY, United Kingdom.

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Classifications MeSH