Amnion-Derived Teno-Inductive Secretomes: A Novel Approach to Foster Tendon Differentiation and Regeneration in an Ovine Model
Citeroni MR., Mauro A., Ciardulli MC., Di Mattia M., El Khatib M., Russo V.
Animal Study on Tendon Injury, published in Front Bioeng Biotechnol (2021) — summary generated from the PubMed abstract.
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
- Level A · Stronger Clinical Evidence
- Level B · Emerging clinical evidence with positive signals
- Level C · Early human research exploring benefits
- Level D · Scientific groundwork from lab and animal studies
- Emerging · Emerging topic under active research
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- Study type
- Animal Study
- Journal
- Front Bioeng Biotechnol (2021)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 33777919
- PMCID
- PMC7991318
- DOI
- 10.3389/fbioe.2021.649288
- Citations
- 25
Abstract (original English)
Regenerative medicine has greatly progressed, but tendon regeneration mechanisms and robust in vitro tendon differentiation protocols remain to be elucidated. Recently, tendon explant co-culture (CO) has been proposed as an in vitro model to recapitulate the microenvironment driving tendon development and regeneration. Here, we explored standardized protocols for production and storage of bioactive tendon-derived secretomes with an evaluation of their teno-inductive effects on ovine amniotic epithelial cells (AECs). Teno-inductive soluble factors were released in culture-conditioned media (CM) only in response to active communication between tendon explants and stem cells (CM CO ). Unsuccessful tenogenic differentiation in AECs was noted when exposed to CM collected from tendon explants (CM FT ) only, whereas CM CO upregulated SCXB, COL I and TNMD transcripts, in AECs, alongside stimulation of the development of mature 3D tendon-like structures enriched in TNMD and COL I extracellular matrix proteins. Furthermore, although the tenogenic effect on AECs was partially inhibited by freezing CM CO , this effect could be recovered by application of an in vivo -like physiological oxygen (2% O 2 ) environment during AECs tenogenesis. Therefore, CM CO can be considered as a waste tissue product with the potential to be used for the development of regenerative bio-inspired devices to inn
What this study does not prove
- • This study does not prove SVF is an approved treatment or a replacement for standard care.
- • This is preclinical work; animal or laboratory results cannot be applied to humans.
Evidence level
Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.
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