MECHANOSITY · Mechanical regulation of cellular behaviour in 3D viscoelastic materials
„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“
- Период
- 2019-09-01 → 2022-08-31
- Финансиране от ЕС
- 239 191 €
- Участници
- 2
- Схема
- MSCA-IF
Линиите свързват координатора с партньорите.
Накратко на български
Вискоеластичността на тъканите, които се държат едновременно като твърди и течни тела, регулира поведението на клетките при процеси като рака. Разбирането на тези механизми помага при разработването на нови биоматериали и инженерството на тъкани.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Mechanical regulation of cellular behaviour in 3D viscoelastic materials
Extracellular matrix (ECM) mechanical properties have emerged as key promoters of processes such as cell migration and epithelial to mesenchymal transition (EMT) in cancer. Despite recent advances in the understanding of cellular ECM sensing machinery, mimicking tissue microenvironments in vitro is highly challenging, and most research has been focused on two dimensional (2D) elastic substrates. However, ECMs are not merely 2D elastic substrates, but rather viscoelastic three-dimensional (3D) materials. All our tissues and organs in our bodies are viscoelastic, behave both as solids and as liquids. Our objective is to understand how the viscoelastic properties of 3D ECMs regulate tissue behaviour. Most research has focused only on the influence of elasticity as the main mechanical property that regulates tissue response. However, little importance has been drawn towards viscoelasticity. The ECM is not merely elastic but is instead both viscous and elastic. Due to its viscoelastic nature, the ECM response is time dependent and highly dynamic and how viscoelasticity affects tissue behaviour is unknown. This project has defined novel mechanonsensing mechanisms that regulate tissue response in in vivo like matrices that had not previously been observed. These mechanisms, due to the inherent viscoelastic nature of tissues, affect many biological fields from morphogenesis to cancer and more translational fields like biomaterials development or tissue engineering. We hypothesized that the viscoelastic nature of tissue was a more determinant mechanical property than stiffness in tissue response due to its dynamic nature and potential adaptability. To address the influence of viscoelasticity, Alberto Elosegui-Artola (the experienced researcher/ Applicant) will develop a set of hydrogels matching the viscoelastic properties of both healthy and malignant breast tissue. With these ideal system Alberto Elosegui-Artola has observed that matrix viscoelasticity regulates mammary epithelial cells migration and proliferation. This project’s results have revealed novel molecular mechanisms that could lead to new therapeutic targets in breast cancer, and also to provide translational opportunities in other disciplines including biomaterials and regenerative medicine.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
Extracellular matrix (ECM) mechanical properties have emerged as key promoters of processes such as cell migration and epithelial to mesenchymal transition (EMT) in cancer. Despite recent advances in the understanding of cellular ECM sensing machinery, mimicking tissue microenvironments in vitro is highly challenging, and most research has been focused on two dimensional (2D) elastic substrates. However, ECMs are not merely 2D elastic substrates, but rather viscoelastic three dimensional (3D) materials. Our objective is to understand how the viscoelastic properties of 3D ECMs regulate cell behaviour. We hypothesize that in viscoelastic materials, counter-intuitively, an increase in viscosity triggers force transduction and gene expression, due to an increase in the load of molecular clutches formed between the ECM and actin. To address the influence of viscoelasticity, Alberto Elosegui-Artola (the experienced researcher/ Applicant) will develop a set of hydrogels matching the viscoelastic properties of both healthy and malignant breast tissue. Then, traction force microscopy will be developed and combined with molecular biology techniques to determine the molecules involved in 3D viscoelasticity sensing. The dynamic behaviour of these molecules will be integrated in a 3D molecular clutch model with the aim to predict cellular migration and force transduction. Model predictions will be validated by performing experiments in 3D viscoelastic gradients on the migration of single cells and spheroids. Lastly, the relevance of the model will be tested by observing if impairing model-predicted force transduction elements prevents EMT transition in cell lines and mouse-derived breast healthy and tumour organoids. This project’s results are expected to reveal molecular interactions that could lead to new therapeutic targets in breast cancer, and also to provide translational opportunities in other disciplines including biomaterials and regenerative medicine.
Оригинален текст от CORDIS (на английски).
Участници
- FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA · BarcelonaКоординаторИспания
- PRESIDENT AND FELLOWS OF HARVARD COLLEGE · CambridgeСъединени щати
Връзки
Данни: CORDIS, © Европейски съюз
