Start, stop, rewind, repeat - cyclic exposure of adipose stromal cells‐derived cartilage organoids to chondrogenic and proliferative cues to achieve scaled‐up and customizable bone formation by endochondral ossification

dc.contributor.authorPfister, Pablo
dc.contributor.authorLhospice, Emilien
dc.contributor.authorGarcía‐García, Andrés
dc.contributor.authorPaillaud, Robert
dc.contributor.authorJung, Sebastian
dc.contributor.authorSchaller, Romain
dc.contributor.authorKappos, Elisabeth A.
dc.contributor.authorJaquiéry, Claude
dc.contributor.authorIsmail, Tarek
dc.contributor.authorSchaefer, Dirk J.
dc.contributor.authorde Wild, Michael
dc.contributor.authorMartin, Ivan
dc.contributor.authorKaempfen, Alexandre
dc.contributor.authorScherberich, Arnaud
dc.contributor.authorMoya, Adrien
dc.date.accessioned2026-02-13T10:54:59Z
dc.date.issued2026
dc.description.abstractDevelopmental tissue engineering (TE) strategies recapitulating endochondral ossification (ECO)—the major ossification pathway in bone development and repair– are a promising avenue for the treatment of critical size and congenital bone defects. In this work, we develop a customizable approach using adipose stromal cells (ASC)‐derived cartilage organoids as building blocks to generate clinically relevant grafts. Our hypothesis is that progenitor cells rather than mature chondrocytes would enable robust cartilage organoids fusion allowing graft tunability and scaling up. Using a cyclic approach alternating chondrogenic and proliferative cues we produce cartilage organoids surrounded by stromal chondrogenic progenitors. When re‐exposed to chondrogenic medium, this perichondrial layer forms new cartilage tissue and acts as a biological cement in between cartilage organoids. A key feature of our approach is the iterative aspect of the protocol, where scaled up cartilage tissues obtained can themselves be used as building blocks to create larger tissue. Finally, in vivo, these grafts remodel efficiently into functional and mechanically apt bone organs mirroring ECO during skeletal development over the course of 24 weeks. Collectively, our findings provide a strong proof of concept of the envisioned TE strategy paving the way for a clinical application in the near future.
dc.identifier.doi10.1002/adhm.202504880
dc.identifier.issn2192-2640
dc.identifier.issn2192-2659
dc.identifier.urihttps://irf.fhnw.ch/handle/11654/55392
dc.identifier.urihttps://doi.org/10.26041/fhnw-15236
dc.language.isoen
dc.publisherWiley
dc.relation.ispartofAdvanced Healthcare Materials
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc610 - Medizin und Gesundheit
dc.titleStart, stop, rewind, repeat - cyclic exposure of adipose stromal cells‐derived cartilage organoids to chondrogenic and proliferative cues to achieve scaled‐up and customizable bone formation by endochondral ossification
dc.type01A - Beitrag in wissenschaftlicher Zeitschrift
dspace.entity.typePublication
fhnw.InventedHereYes
fhnw.ReviewTypeAnonymous ex ante peer review of a complete publication
fhnw.affiliation.hochschuleHochschule für Life Sciences FHNWde_CH
fhnw.affiliation.institutInstitut für Medizintechnik und Medizininformatikde_CH
fhnw.oastatus.auroraVersion: Accepted *** Embargo: 12 months *** Licence: None *** URL: https://v2.sherpa.ac.uk/id/publication/21321
fhnw.openAccessCategoryHybrid
fhnw.paginatione04880-e04880
fhnw.publicationStatePublished
fhnw.targetcollection7bbb4209-e450-4feb-ad5d-ea711f087e13
relation.isAuthorOfPublication3fe309a1-bd6b-4888-9f0d-b242a7c95e43
relation.isAuthorOfPublication135938a9-969d-4ea3-9bb2-7ff1d77554cb
relation.isAuthorOfPublication.latestForDiscovery3fe309a1-bd6b-4888-9f0d-b242a7c95e43
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