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BE-ECM

Bioreactors for Enhanced Extra Cellular Matrix elaboration (BE-ECM)

Brief description

Main topic: in vitro elastomeric models to investigate soft tissue mechanobiology.
Three macro-areas are recognized as crucial to understand the factors that drive tissue repair and de novo tissue formation: I) mechanical models able to correlate the macro, meso and micro scales, II) tissue growth models with the ability to correlate mechanics and tissue elaboration, III) scaffold degradation models able to correlate mass loss with mechanical loads and deformations. The BE-ECM research line, integrated by NET-IBA and NET-MTG, tries to address these three critical topics by introducing and perfecting physical, in-vitro models able to study tissue growth, cell behavior and biomaterials degradation.

Impact:

Potential impact of this research might involve improved capacity to:

– simulate endogenous tissue growth on engineered scaffolds under mechanical load and deformation;

– simulate in vivo degradation of engineered scaffolds;

– investigate the impact of material topological and mechanical cues on ECM elaboration.

– investigate how cell signaling and biochemistry interact to guide cell behavior in biomaterials

This in vitro modeling ability might allow to expand the understanding of biomaterials mechanobiology and might allow to assess, using simplified tissue surrogates, the efficacy of novel tissue engineering strategies. Examples of these modeling efforts include: mechanisms to accelerate tissue growth, solutions to modulate material degradation characteristics, topological cues to dictate cell differentiation and lineage.

 

Pipeline

  • CLINICAL
    NEED
  • DISEASES
    ANALYSIS
  • DISCOVERY
  • PRECLINICAL
    VALIDATION
  • PRECLINICAL
    DEVELOPMENT
  • CLINICAL
    STUDIES
BE-ECM: Integrated empirical and numerical approach to study extracellular matrix synthesis and elaboration in soft tissue. Electrospun polymeric scaffolds microintegrated with cells are generally accepted as in vitro model to elucidate the complex mechanism of extracellular matrix (ECM) synthesis in vivo. Examples of cardiac tissue surrogates based on biocompatible fibrous scaffolds include cardiac patches, vascular grafts, heart valves and engineered chordae tendineae processed by electrospinning and microintegrated by electrospray. Custom made bioreactors are used to investigate the influence of mechanical load on ECM elaboration. Both mechanical and topological cues are widely recognized as a decisive factors in ECM formation and elaboration. Previous results have shown that de novo collagen production is sensitive to the applied strain level and it is also a function of the mesoscopic niche created by the scaffold micro-architecture. ECM formation and elaboration is evaluated with a multi-scale empirical and numerical approach that includes in-plane mechanical response of the material, micro-architecture characterization via electron microscopy and digital image analysis, histological evaluation and nuclear aspect ratio estimate.

Principal Investigator

Contact

adamore@fondazionerimed.com

Research group:

Therapeutic area:

Products:
ATMPMedical devices & tissue engineering

 

Collaborations:
UK Dementia Research Institute (UK DRI) – King’s College London, Londra, Regno Unito
European Brain Research Institute Rita Levi Montalcini (EBRI), Roma, Italia
Scuola Normale Superiore di Pisa (SNS), Pisa, Italia
Dipartimento di Medicina Molecolare – Università degli Studi di Pavia, Pavia, Italia
Covid19-NMR International Consortium

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