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doi:10.22028/D291-44107
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Titel: | Vesicle-bound regulatory RNAs are associated with tissue aging |
VerfasserIn: | Kern, Fabian ![]() Kuhn, Thomas ![]() Ludwig, Nicole Simon, Martin Gröger, Laura ![]() Fabis, Natalie Salhab, Abdulrahman ![]() Fehlmann, Tobias ![]() Hahn, Oliver Engel, Annika ![]() Koch, Marcus Koehler, Jana Winek, Katarzyna Soreq, Hermona Fuhrmann, Gregor ![]() Wyss-Coray, Tony Meese, Eckart Laschke, Matthias W. ![]() Keller, Andreas ![]() |
Sprache: | Englisch |
Verlag/Plattform: | bioRxiv |
Erscheinungsjahr: | 2021 |
Freie Schlagwörter: | non-coding RNA tissue aging extracellular vesicles plasma exosomes |
DDC-Sachgruppe: | 610 Medizin, Gesundheit |
Dokumenttyp: | Sonstiges |
Abstract: | Previous work on murine models and human demonstrated global as well as tissue-specific molecular aging trajectories in solid tissues and body fluids1–8. Extracellular vesicles like exosomes play a crucial role in communication and information exchange in between such systemic factors and solid tissues9,10. We sequenced freely circulating and vesicle-bound small regulatory RNAs in mice at five time points across the average life span from 2 to 18 months. Intriguingly, each small RNA class exhibits unique aging patterns, which showed differential signatures between vesicle-bound and freely circulating molecules. In particular, tRNA fragments showed overall highest correlation with aging which also matched well between sample types, facilitating age prediction with non-negative matrix factorization (86% accuracy). Interestingly, rRNAs exhibited inverse correlation trajectories between vesicles and plasma while vesicle-bound microRNAs (miRNAs) were exceptionally strong associated with aging. Affected miRNAs regulate the inflammatory response and transcriptional processes, and adipose tissues show considerable effects in associated gene regulatory modules. Finally, nanoparticle tracking and electron microscopy suggest a shift from overall many small to fewer but larger vesicles in aged plasma, potentially contributing to systemic aging trajectories and affecting the molecular aging of organs. |
DOI der Erstveröffentlichung: | 10.1101/2021.05.07.443093 |
URL der Erstveröffentlichung: | https://doi.org/10.1101/2021.05.07.443093 |
Link zu diesem Datensatz: | urn:nbn:de:bsz:291--ds-441074 hdl:20.500.11880/39452 http://dx.doi.org/10.22028/D291-44107 |
Datum des Eintrags: | 23-Jan-2025 |
Bezeichnung des in Beziehung stehenden Objekts: | Supplementary material |
In Beziehung stehendes Objekt: | https://www.biorxiv.org/content/biorxiv/early/2021/05/08/2021.05.07.443093/DC1/embed/media-1.pdf?download=true https://www.biorxiv.org/content/biorxiv/early/2021/05/08/2021.05.07.443093/DC1/embed/media-1.pdf?download=true https://www.biorxiv.org/content/biorxiv/early/2021/05/08/2021.05.07.443093/DC3/embed/media-3.xlsx?download=true |
Bemerkung/Hinweis: | Preprint |
Fakultät: | M - Medizinische Fakultät NT - Naturwissenschaftlich- Technische Fakultät |
Fachrichtung: | M - Chirurgie M - Humangenetik M - Medizinische Biometrie, Epidemiologie und medizinische Informatik NT - Biowissenschaften NT - Pharmazie |
Professur: | M - Univ.-Prof. Dr. Andreas Keller M - Prof. Dr. Eckart Meese M - Prof. Dr. Michael D. Menger NT - Jun.-Prof. Dr. Gregor Fuhrmann NT - Prof. Dr. Jörn Walter |
Sammlung: | SciDok - Der Wissenschaftsserver der Universität des Saarlandes |
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