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dc.contributor.author
Balic, Anamaria
dc.contributor.author
Perver, Dilara
dc.contributor.author
Pagella, Pierfrancesco
dc.contributor.author
Rehrauer, Hubert
dc.contributor.author
Stadlinger, Bernd
dc.contributor.author
Moor, Andreas
dc.contributor.author
Vogel, Viola
dc.contributor.author
Mitsiadis, Thimios A.
dc.date.accessioned
2024-01-17T13:40:41Z
dc.date.available
2024-01-15T10:52:38Z
dc.date.available
2024-01-17T13:40:41Z
dc.date.issued
2023-02-18
dc.identifier.other
10.1101/2023.02.15.528696
en_US
dc.identifier.uri
http://hdl.handle.net/20.500.11850/652630
dc.description.abstract
The carious lesion is a bacteria caused destruction of tooth mineralized matrices marked by concurrent tissue reparative and immune responses in the dental pulp. While major molecular players in tooth pulp decay have been uncovered, a detailed map of the molecular and cellular landscape of the diseased pulp is still missing. Here we used single-cell RNA sequencing analysis, to generate a comprehensive single-cell atlas of the carious human dental pulp tissue. Our data demonstrated modifications in various cell clusters of the carious pulp, such as immune cells, mesenchymal stem cells (MSC) and fibroblasts, when compared to the healthy dental pulp. These changes include upregulation of genes encoding extracellular matrix (ECM) components and the enrichment of the fibroblast cluster with myofibroblasts. Assessment of the Fibronectin fibres’ mechanical strain showed a significant tension reduction in the carious human pulp, compared to the healthy one. Collectively, the present data demonstrate molecular, cellular and biomechanical alterations in the carious pulp tissue, indicative of extensive ECM remodelling and reminiscent of fibrosis observed in other organs.
en_US
dc.language.iso
en
en_US
dc.publisher
Cold Spring Harbor Laboratory
en_US
dc.subject
Single-cell RNA sequencing
en_US
dc.subject
Tooth
en_US
dc.subject
Dental pulp
en_US
dc.subject
Caries
en_US
dc.subject
Extracellular matrix
en_US
dc.subject
Human
en_US
dc.subject
Fibronectin
en_US
dc.subject
Collagen
en_US
dc.subject
Tenascin-C
en_US
dc.subject
Immune system
en_US
dc.title
Single-cell transcriptomics analysis reveals extracellular matrix remodelling in carious human dental pulp
en_US
dc.type
Working Paper
ethz.journal.title
bioRxiv
ethz.size
31 p.
en_US
ethz.publication.place
Cold Spring Harbor, NY
en_US
ethz.publication.status
published
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02060 - Dep. Biosysteme / Dep. of Biosystems Science and Eng.::09711 - Moor, Andreas / Moor, Andreas
en_US
ethz.leitzahl
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00012 - Lehre und Forschung::00007 - Departemente::02060 - Dep. Biosysteme / Dep. of Biosystems Science and Eng.::09711 - Moor, Andreas / Moor, Andreas
en_US
ethz.leitzahl.certified
ETH Zürich::00002 - ETH Zürich::00003 - Schulleitung und Dienste::00022 - Bereich VP Forschung / Domain VP Research::02207 - Functional Genomics Center Zurich / Functional Genomics Center Zurich
ethz.date.deposited
2024-01-15T10:52:38Z
ethz.source
FORM
ethz.eth
yes
en_US
ethz.availability
Metadata only
en_US
ethz.rosetta.installDate
2024-01-17T13:40:43Z
ethz.rosetta.lastUpdated
2024-02-03T08:51:55Z
ethz.rosetta.versionExported
true
ethz.COinS
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