Please use this identifier to cite or link to this item:
https://hdl.handle.net/10316/100614
DC Field | Value | Language |
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dc.contributor.author | Schüler, Svenja C | - |
dc.contributor.author | Kirkpatrick, Joanna M | - |
dc.contributor.author | Schmidt, Manuel | - |
dc.contributor.author | Santinha, Deolinda | - |
dc.contributor.author | Koch, Philipp | - |
dc.contributor.author | Di Sanzo, Simone | - |
dc.contributor.author | Cirri, Emilio | - |
dc.contributor.author | Hemberg, Martin | - |
dc.contributor.author | Ori, Alessandro | - |
dc.contributor.author | von Maltzahn, Julia | - |
dc.date.accessioned | 2022-07-07T09:35:59Z | - |
dc.date.available | 2022-07-07T09:35:59Z | - |
dc.date.issued | 2021 | - |
dc.identifier.issn | 22111247 | pt |
dc.identifier.uri | https://hdl.handle.net/10316/100614 | - |
dc.description.abstract | During aging, the regenerative capacity of skeletal muscle decreases due to intrinsic changes in muscle stem cells (MuSCs) and alterations in their niche. Here, we use quantitative mass spectrometry to characterize intrinsic changes in the MuSC proteome and remodeling of the MuSC niche during aging. We generate a network connecting age-affected ligands located in the niche and cell surface receptors on MuSCs. Thereby, we reveal signaling by integrins, Lrp1, Egfr, and Cd44 as the major cell communication axes perturbed through aging. We investigate the effect of Smoc2, a secreted protein that accumulates with aging, primarily originating from fibro-adipogenic progenitors. Increased levels of Smoc2 contribute to the aberrant Integrin beta-1 (Itgb1)/mitogen-activated protein kinase (MAPK) signaling observed during aging, thereby causing impaired MuSC functionality and muscle regeneration. By connecting changes in the proteome of MuSCs to alterations of their niche, our work will enable a better understanding of how MuSCs are affected during aging. | pt |
dc.language.iso | eng | pt |
dc.relation | Federal Government of Germany and the State of Thuringia | pt |
dc.relation | grant from the Deutsche Forschungsgemeinschaft to J.v.M. (MA-3975/2-1). | pt |
dc.relation | Research Training Group ProMoAge (GRK 2155 | pt |
dc.relation | Else Kro¨ ner-Fresenius-Stiftung (award number 2019_A79) | pt |
dc.relation | Deutsches Zentrum f€ur Herz-Kreislaufforschung (award number 81X2800193) | pt |
dc.relation | Fritz Thyssen Foundation (award number 10.20.1.022MN) | pt |
dc.rights | openAccess | pt |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | pt |
dc.subject | aging | pt |
dc.subject | extracellular matrix | pt |
dc.subject | Integrin | pt |
dc.subject | muscle stem cell | pt |
dc.subject | niche | pt |
dc.subject | pERK | pt |
dc.subject | proteomics | pt |
dc.subject | satellite cell | pt |
dc.subject | skeletal muscle | pt |
dc.subject | Smoc2 | pt |
dc.subject.mesh | Cell Differentiation | pt |
dc.subject.mesh | Extracellular Matrix | pt |
dc.subject.mesh | Humans | pt |
dc.subject.mesh | Integrins | pt |
dc.subject.mesh | Muscle, Skeletal | pt |
dc.subject.mesh | Stem Cells | pt |
dc.title | Extensive remodeling of the extracellular matrix during aging contributes to age-dependent impairments of muscle stem cell functionality | pt |
dc.type | article | - |
degois.publication.firstPage | 109223 | pt |
degois.publication.issue | 10 | pt |
degois.publication.title | Cell Reports | pt |
dc.peerreviewed | yes | pt |
dc.identifier.doi | 10.1016/j.celrep.2021.109223 | pt |
degois.publication.volume | 35 | pt |
dc.date.embargo | 2021-01-01 | * |
uc.date.periodoEmbargo | 0 | pt |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
item.openairetype | article | - |
item.cerifentitytype | Publications | - |
item.grantfulltext | open | - |
item.fulltext | Com Texto completo | - |
item.languageiso639-1 | en | - |
Appears in Collections: | I&D CNC - Artigos em Revistas Internacionais FMUC Medicina - Artigos em Revistas Internacionais |
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File | Description | Size | Format | |
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1-s2.0-S221112472100574X-main.pdf | 6.85 MB | Adobe PDF | View/Open |
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