Summary
Interaction between cells and their mechanical microenvironment plays a key role in the regulation of development, physiology and disease. Cell behaviour is also regulated by the dimensionality of the microenvironment: 2D cultures display
biological traits that generally differ from those of 3D tissues, thus limiting their potential in biomedical research. This
limitation has been addressed by the recent development of Organoids, which faithfully preserve a number of distinctive
tissue traits. Still, current biophysical tools and conceptual frameworks are not yet suitable to probe and understand the
mechanobiology of 3D organoid systems.
This project aims to study and manipulate the mechanobiology of normal gut and colorectal cancer organoids. We will
develop tools to quantify the 3D stresses applied by an organoid embedded in a gel. By measuring its 3D surface stresses
and Young’s modulus we will quantify its interstitial pressure and contractility, key parameters in organ growth and tumour
progression.
Pressure and contractility will be related with key biological parameters such as geometry, cell adhesion and proliferation.
We will fluorescently tag proteins in the organoids that will allow us to track individual cells, as well as monitoring their
polarization and adhesion. The relationship between mechanics, geometry, and cell function will be further assessed by
chemically reducing proliferation, mechanical stresses and adhesion.
We will also modify the mechanical state of the organoids through optogenetic means. We will express proteins in the cells
to control Rho-GTPases upon illumination, thereby steering the local stresses at will. We will modify organoid pressure,
contractility and geometry and study their influence on the phenotype.
As organoids emerge as novel tools in biomedical research, we expect that studying and manipulating their mechanobiology
will bring key insight into disease and development processes, and potential new therapeutic targets.
biological traits that generally differ from those of 3D tissues, thus limiting their potential in biomedical research. This
limitation has been addressed by the recent development of Organoids, which faithfully preserve a number of distinctive
tissue traits. Still, current biophysical tools and conceptual frameworks are not yet suitable to probe and understand the
mechanobiology of 3D organoid systems.
This project aims to study and manipulate the mechanobiology of normal gut and colorectal cancer organoids. We will
develop tools to quantify the 3D stresses applied by an organoid embedded in a gel. By measuring its 3D surface stresses
and Young’s modulus we will quantify its interstitial pressure and contractility, key parameters in organ growth and tumour
progression.
Pressure and contractility will be related with key biological parameters such as geometry, cell adhesion and proliferation.
We will fluorescently tag proteins in the organoids that will allow us to track individual cells, as well as monitoring their
polarization and adhesion. The relationship between mechanics, geometry, and cell function will be further assessed by
chemically reducing proliferation, mechanical stresses and adhesion.
We will also modify the mechanical state of the organoids through optogenetic means. We will express proteins in the cells
to control Rho-GTPases upon illumination, thereby steering the local stresses at will. We will modify organoid pressure,
contractility and geometry and study their influence on the phenotype.
As organoids emerge as novel tools in biomedical research, we expect that studying and manipulating their mechanobiology
will bring key insight into disease and development processes, and potential new therapeutic targets.
Unfold all
/
Fold all
More information & hyperlinks
| Web resources: | https://cordis.europa.eu/project/id/797621 |
| Start date: | 01-09-2019 |
| End date: | 31-08-2021 |
| Total budget - Public funding: | 158 121,60 Euro - 158 121,00 Euro |
Cordis data
Original description
Interaction between cells and their mechanical microenvironment plays a key role in the regulation of development, physiology and disease. Cell behaviour is also regulated by the dimensionality of the microenvironment: 2D cultures displaybiological traits that generally differ from those of 3D tissues, thus limiting their potential in biomedical research. This
limitation has been addressed by the recent development of Organoids, which faithfully preserve a number of distinctive
tissue traits. Still, current biophysical tools and conceptual frameworks are not yet suitable to probe and understand the
mechanobiology of 3D organoid systems.
This project aims to study and manipulate the mechanobiology of normal gut and colorectal cancer organoids. We will
develop tools to quantify the 3D stresses applied by an organoid embedded in a gel. By measuring its 3D surface stresses
and Young’s modulus we will quantify its interstitial pressure and contractility, key parameters in organ growth and tumour
progression.
Pressure and contractility will be related with key biological parameters such as geometry, cell adhesion and proliferation.
We will fluorescently tag proteins in the organoids that will allow us to track individual cells, as well as monitoring their
polarization and adhesion. The relationship between mechanics, geometry, and cell function will be further assessed by
chemically reducing proliferation, mechanical stresses and adhesion.
We will also modify the mechanical state of the organoids through optogenetic means. We will express proteins in the cells
to control Rho-GTPases upon illumination, thereby steering the local stresses at will. We will modify organoid pressure,
contractility and geometry and study their influence on the phenotype.
As organoids emerge as novel tools in biomedical research, we expect that studying and manipulating their mechanobiology
will bring key insight into disease and development processes, and potential new therapeutic targets.
Status
CLOSEDCall topic
MSCA-IF-2017Update Date
28-04-2024
Images
No images available.
Geographical location(s)
Search
