METAFORA · Miniaturised Metabolomics Platform for Microvascular Research
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2016-10-01 → 2018-09-30
- EU contribution
- €177,599
- Participants
- 1
- Scheme
- MSCA-IF-EF-CAR
Lines connect the coordinator with its partners.
Results in brief
Miniaturised Metabolomics Platform for Microvascular Research
Microvascular disease is a chronic disease which lacks efficient treatment because the disease mechanism is still unclear. Microvascular disease is the result of continued exposure of the small blood vessels in human body to high blood pressure, obesity and diabetes. It leads to the progressive loss of tissue capillaries, tissue-ischemia and fibrosis. As a consequence, the damaged vessels are a main cause of morbidity of the elderly, leading to end-organ diseases including heart failure, kidney failure, dementia, and beta cell failure in pancreas. Worldwide, approximately 80% of all diabetic patients develop retinopathy, 20% develop neuropathy, and 40% develop nephropathy. A novel approach is needed to study the pathology of microvascular disease. In the last 10 years extracellular vesicles emerged as a new target in disease biomarkers and the keys to disease mechanisms. These nanosized vesicles are produced by all cells and represent an information rich matrix containing proteins, mRNA and metabolites of the parental cell. The exosomes can be found in all body fluids (blood, urine, tears) and that is why they are possible to access without invasive procedures. There is increasing evidence that detecting blood extracellular vesicles of epithelial and platelet origin may present very useful non-invasive signature for the onset of microvascular disease. The application of metabolomics methodologies and extracellular vesicles to the study of microvascular disease can increase our understanding of the pathophysiological processes involved and this should help to identify potential biomarkers to diagnose disease and develop new therapeutic strategies. Isolating and separating extracellular vesicles from blood, however, is very challenging. This project proposed a new way to resolve this problem.
Data: CORDIS, © European Union
Project objective
Preventing and treating progressive microvascular loss (i.e. rarefaction) is a major challenge in cardiovascular medicine. Microvascular disease is a multifactorial disease with no effective treatment. Long-term exposure to adverse metabolic and haemodynamic conditions such as hypertension, obesity and diabetes can cause microvascular destabilisation, loss of tissue capillaries, and eventual organ failure. Interestingly, not all diabetic patients develop kidney failure. The missing link to developing effective strategies for treating multifactorial diseases, including microvascular disease, is detailed mechanistic insight into the relationship between disease pathogenesis at the organ/cellular level at the systemic/organism level. This project, METAFORA, aims to develop novel and analytical technologies to allow a new approach to understand the pathology of microvascular disease. METAFORA will develop a miniaturized metabolomics workflow to study metabolic pathways in an in-vitro microfluidic 3D microvasculature platform with organotypic functionality (the so-called organ-on-a-chip) to create personalised in-vitro models based on patient-derived human cells. This platform will enable the assessment of biochemical disease processes at the cell/organ level in the ‘whole-patient’ context by perfusing the patient’s own blood through the vasculature model.METAFORA will use and optimize a novel separation and preconcentration method, depletion zone isotachophoresis, for the miniaturised analytical platform, which will be combined with mass spectrometry for metabolite profiling.
Original text from CORDIS.
Participants
- UNIVERSITEIT LEIDEN · LeidenCoordinatorNetherlands
Links
- View on CORDIS
- DOI: 10.3030/709077
- http://yuliya.exosome.nl/publications/
- https://ec.europa.eu/research-and-innovation/en/projects/success-stories/all/decoding-bubbles-bodily-fluids-diagnose-disease
Data: CORDIS, © European Union
