CREATION | Mechanobiological optimization of regeneration in cell-enriched construct implants within degenerative Cartilages: a defect Repair method through restoring Energy AbsorpTION

Summary
Knee cartilage defects and consequent degeneration contribute to the development of osteoarthritis (OA). OA affects the mechanical integrity of the tissue, whose main function is to absorb shock and minimize peak loads in the underlying subchondral bone.
Tissue engineering methods propose solutions to OA by implanting chondrocyte cell-enriched hydrogel/scaffold constructs within degenerative cartilage defects. By applying mechanical loads to stimulate the cells within the constructs, they initiate cartilage extracellular matrix (ECM) synthesis. The mechanical environment of the cell-seeded construct has a crucial role in defining the quality and quantity of the regenerated ECM. This will determine the mechanical performance of the cartilage tissue. Indeed, any repair method has to aim at restoring the unique cartilage mechanics, in particular, the energy absorption capacity.
This project aims at restoring energy absorption of degenerative cartilage by optimizing regeneration in cell-enriched construct implants. The goal will be pursued by developing an in-silico framework for mechanobiological modelling of the regeneration and degeneration in the cartilage-implant compound during loading. Unique in the in-silico framework is the simultaneous modelling of regenerative and degenerative processes through adaptive modelling of the ECM. An innovative regeneration algorithm will be developed and integrated with a previously developed degeneration model. The adaptive model will then be used in an optimization scheme to minimize differences between energy absorption of construct implant and native human cartilage. An iterative performance evaluation is foreseen in comparison with biological experiments.
In collaboration with the participating research groups and using my background, I will have a unique chance to take a step forward in furthering insights on OA disease process. The anticipated collaborations and training will contribute to making me a mature researcher.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/893771
Start date: 01-09-2020
End date: 31-08-2022
Total budget - Public funding: 178 320,00 Euro - 178 320,00 Euro
Cordis data

Original description

Knee cartilage defects and consequent degeneration contribute to the development of osteoarthritis (OA). OA affects the mechanical integrity of the tissue, whose main function is to absorb shock and minimize peak loads in the underlying subchondral bone.
Tissue engineering methods propose solutions to OA by implanting chondrocyte cell-enriched hydrogel/scaffold constructs within degenerative cartilage defects. By applying mechanical loads to stimulate the cells within the constructs, they initiate cartilage extracellular matrix (ECM) synthesis. The mechanical environment of the cell-seeded construct has a crucial role in defining the quality and quantity of the regenerated ECM. This will determine the mechanical performance of the cartilage tissue. Indeed, any repair method has to aim at restoring the unique cartilage mechanics, in particular, the energy absorption capacity.
This project aims at restoring energy absorption of degenerative cartilage by optimizing regeneration in cell-enriched construct implants. The goal will be pursued by developing an in-silico framework for mechanobiological modelling of the regeneration and degeneration in the cartilage-implant compound during loading. Unique in the in-silico framework is the simultaneous modelling of regenerative and degenerative processes through adaptive modelling of the ECM. An innovative regeneration algorithm will be developed and integrated with a previously developed degeneration model. The adaptive model will then be used in an optimization scheme to minimize differences between energy absorption of construct implant and native human cartilage. An iterative performance evaluation is foreseen in comparison with biological experiments.
In collaboration with the participating research groups and using my background, I will have a unique chance to take a step forward in furthering insights on OA disease process. The anticipated collaborations and training will contribute to making me a mature researcher.

Status

CLOSED

Call topic

MSCA-IF-2019

Update Date

28-04-2024
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Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.2. Nurturing excellence by means of cross-border and cross-sector mobility
H2020-MSCA-IF-2019
MSCA-IF-2019