H2020Individual fellowship2017–2019

PROM · Pregnancy and Reproduction Organ-on-a-chip Models

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2017-07-01 → 2019-06-30
EU contribution
€195,455
Participants
1
Scheme
MSCA-IF-EF-RI

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Results in brief

Pregnancy and Reproduction Organ-on-a-chip Models

PreTerm Birth (PTB) occurs before 37 weeks of gestation. Of 60,000 babies born prematurely every year in UK, ~1,400 die. Premature babies show increased risks of long term neurodevelopmental deficits and chronic diseases. Preterm Rupture of the foetal Membranes (PROM) is a syndrome attributable to multiple factor. Evidences linked environmental toxicant exposure and infection with a decreased fertility and an increase PTB rate. Studies of these topics suffered for limits of in vitro cell culture (e.g. absence of extracellular environment, dilution) and anatomical, physiological, endocrine differences between human and animal models. Long term goal of this project is to create Organ-on-a-Chip (OoC) models of the human endometrium and the human foetal membranes to assess the effects of environmental insults, such as infection or inflammation, to exacerbate preterm birth. An overarching goal is to utilize these OoC models to identify personalized therapy to improve and preserve fertility. Thanks to this fellowship, I thus designed and developed 2 microfluidic systems that allow to grow human, patient-derived cell of the uterus and the foetal membranes in a controlled environment to recreate their natural physiological functions. These devices have been designed with inputs from experts in the field of microfluidics, infectious diseases and reproductive biology and toxicology. In parallel I focused on early embryo development to design a new device for in vitro fertilization. The results of this research have been presented at several international conferences and have been summarized in 1 PCT patent, 3 published papers and 2 papers in preparation. In these 2 years, I have learnt analytical methods (qPCR, ELISA, Mass Spectrometry, proteomics, metabolomics) and tissue culture techniques (embryo culture and cell isolation protocols) that were not part of my engineering background. I also established new collaborations in the field of manufacturing, sustainable plastics and tissue engineering, to define new approaches for the fabrication of the new generation of organs-on-a-chip and for the integration of biocompatible scaffold in the microfluidic device.

Data: CORDIS, © European Union

Project objective

PreTerm Birth (PTB) occurs before 37 weeks of gestation. Of 60,000 babies born prematurely every year in UK, ~1,400 die. Premature babies show increased risks of long term neurodevelopmental deficits and chronic diseases.Preterm Rupture of the foetal Membranes (PROM) is a syndrome attributable to multiple factor. Evidences linked environmental toxicant exposure and infection with a decreased fertility and an increase PTB rate.Studies of these topics suffered for limits of in vitro cell culture (e.g. absence of extracellular environment, dilution) and anatomical, physiological, endocrine differences between human and animal models. Long term goal of this project is to create Organ-on-a-Chip (OoC) models of the human endometrium and the human foetal membranes to assess the effects of environmental insults, such as infection or inflammation, to exacerbate preterm birth. An overarching goal is to utilize these OoC models to identify personalized therapy to improve and preserve fertility.This project aims to1.Implement an OoC model to replicate the physiology of the human endometrium and the development of the foetal membranes during pregnancy. This will be achieved by adding human amniotic epithelial, chorionic trophoblasts and maternal macrophages in the existing OoC.2.Define the individual contributions of each cell type in the endometrium to paracrine signalling events that lead to PTB. A sub-micrometric polymeric, porous membrane will be integrated in the chip, will allow chemical communication between the cellular compartments of the OoC, will support formation of cell layers and will favour close proximity between the different cell types.3.Monitor metabolic activity and identify PTB biomarkers. Changes in metabolic activity of each cell types, biomarkers of infection and inflammation in response to unknown stressors (e.g. bacteria/ toxins/chemotherapy) will be identified by downstream collection of effluents and direct single cell sensing.

Original text from CORDIS.

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Data: CORDIS, © European Union