Ossified blood vessels in primary familial brain calcification elicit a neurotoxic astrocyte response.


Journal

Brain : a journal of neurology
ISSN: 1460-2156
Titre abrégé: Brain
Pays: England
ID NLM: 0372537

Informations de publication

Date de publication:
01 04 2019
Historique:
received: 10 08 2018
revised: 07 12 2018
accepted: 26 12 2018
pubmed: 26 2 2019
medline: 18 12 2019
entrez: 27 2 2019
Statut: ppublish

Résumé

Brain calcifications are commonly detected in aged individuals and accompany numerous brain diseases, but their functional importance is not understood. In cases of primary familial brain calcification, an autosomally inherited neuropsychiatric disorder, the presence of bilateral brain calcifications in the absence of secondary causes of brain calcification is a diagnostic criterion. To date, mutations in five genes including solute carrier 20 member 2 (SLC20A2), xenotropic and polytropic retrovirus receptor 1 (XPR1), myogenesis regulating glycosidase (MYORG), platelet-derived growth factor B (PDGFB) and platelet-derived growth factor receptor β (PDGFRB), are considered causal. Previously, we have reported that mutations in PDGFB in humans are associated with primary familial brain calcification, and mice hypomorphic for PDGFB (Pdgfbret/ret) present with brain vessel calcifications in the deep regions of the brain that increase with age, mimicking the pathology observed in human mutation carriers. In this study, we characterize the cellular environment surrounding calcifications in Pdgfbret/ret animals and show that cells around vessel-associated calcifications express markers for osteoblasts, osteoclasts and osteocytes, and that bone matrix proteins are present in vessel-associated calcifications. Additionally, we also demonstrate the osteogenic environment around brain calcifications in genetically confirmed primary familial brain calcification cases. We show that calcifications cause oxidative stress in astrocytes and evoke expression of neurotoxic astrocyte markers. Similar to previously reported human primary familial brain calcification cases, we describe high interindividual variation in calcification load in Pdgfbret/ret animals, as assessed by ex vivo and in vivo quantification of calcifications. We also report that serum of Pdgfbret/ret animals does not differ in calcification propensity from control animals and that vessel calcification occurs only in the brains of Pdgfbret/ret animals. Notably, ossification of vessels and astrocytic neurotoxic response is associated with specific behavioural and cognitive alterations, some of which are associated with primary familial brain calcification in a subset of patients.

Identifiants

pubmed: 30805583
pii: 5364607
doi: 10.1093/brain/awz032
pmc: PMC6439320
doi:

Substances chimiques

Proto-Oncogene Proteins c-sis 0
SLC20A2 protein, human 0
Sodium-Phosphate Cotransporter Proteins, Type III 0
XPR1 protein, human 0
Xenotropic and Polytropic Retrovirus Receptor 0
Xpr1 protein, mouse 0
Receptor, Platelet-Derived Growth Factor beta EC 2.7.10.1

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

885-902

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL071625
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL145536
Pays : United States
Organisme : NINDS NIH HHS
ID : R35 NS097261
Pays : United States

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

© The Author(s) (2019). Published by Oxford University Press on behalf of the Guarantors of Brain.

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Auteurs

Yvette Zarb (Y)

Department of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Neuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.

Ulrike Weber-Stadlbauer (U)

Institute of Veterinary Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich University, Zurich, Switzerland.

Daniel Kirschenbaum (D)

Department of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Diana Rita Kindler (DR)

Institute of Neuropathology, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Juliet Richetto (J)

Institute of Veterinary Pharmacology and Toxicology, University of Zurich-Vetsuisse, Zurich University, Zurich, Switzerland.

Daniel Keller (D)

Department of Biomedical Engineering, ETH and University of Zurich, Zurich, Switzerland.

Rosa Rademakers (R)

Institute of Diagnostic and Interventional Radiology, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Dennis W Dickson (DW)

Institute of Diagnostic and Interventional Radiology, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Andreas Pasch (A)

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.

Tatiana Byzova (T)

Calciscon AG, Nidau-Biel, Switzerland.

Khayrun Nahar (K)

Department of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Fabian F Voigt (FF)

Neuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.
Brain Research Institute, Zurich University, Zurich, Switzerland.

Fritjof Helmchen (F)

Neuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.
Brain Research Institute, Zurich University, Zurich, Switzerland.

Andreas Boss (A)

Department of Biomedical Engineering, ETH and University of Zurich, Zurich, Switzerland.

Adriano Aguzzi (A)

Department of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Jan Klohs (J)

Institute of Neuropathology, Zurich University Hospital, Zurich University, Zurich, Switzerland.

Annika Keller (A)

Department of Neurosurgery, Clinical Neuroscience Center, Zurich University Hospital, Zurich University, Zurich, Switzerland.
Neuroscience Center Zurich (ZNZ), University of Zurich and ETH Zurich, Zurich, Switzerland.

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Classifications MeSH