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Revealing cellular behavior with single-cell multi-omics

Chemical reactions govern cellular behavior, and are revealed by analysis of small molecules involved in intracellular metabolism. Individual cells in biological systems continuously adapt to improve survival and biological functi... ver más

31/08/2027

2M€

Presupuesto del proyecto: 2M€

Líder del proyecto

UPPSALA UNIVERSITET No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Financiación concedida El organismo HORIZON EUROPE notifico la concesión del proyecto el día 2022-04-20

Línea de financiación objetivo El proyecto se financió a través de la siguiente ayuda:

ERC-2021-STG: ERC STARTING GRANTS

I+D

Cerrada hace 3 años

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1 Participantes

2.50M€ | Lider

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Últimas noticias

29-11-2024: IDAE En las últimas 48 horas el Organismo IDAE ha otorgado 4 concesiones

29-11-2024: ECE En las últimas 48 horas el Organismo ECE ha otorgado 2 concesiones

29-11-2024: CMVAMADRID En las últimas 48 horas el Organismo CMVAMADRID ha otorgado 37 concesiones

Duración del proyecto: 64 meses Fecha Inicio: 2022-04-20
Fecha Fin: 2027-08-31

Líder del proyecto

UPPSALA UNIVERSITET

TRL 4-5

Presupuesto del proyecto 2M€

Descripción del proyecto Chemical reactions govern cellular behavior, and are revealed by analysis of small molecules involved in intracellular metabolism. Individual cells in biological systems continuously adapt to improve survival and biological function, making them chemically and behaviorally heterogeneous. Unraveling this heterogeneity is essential to realize the correlation to disease state and health, but it is masked in bulk analyses of millions of cells. I propose to develop a groundbreaking analytical approach for multi-omics of living individual cells to reveal variability in cellular behavior. This will be achieved by coupling a microfluidic device that enables controlled chemical exposure of a cell, to an efficient ionization probe for on-line time-resolved mass spectrometric measurements. By measuring the dynamics of each cell’s metabolome, lipidome, and secretome, novel insights into heterogeneity in intracellular activities will be gained. In addition, the level of heterogeneity will be uncovered through correlation with the cell’s transcriptome. A special emphasis will be given to characterize individual β-cells that are key regulators of blood glucose by insulin secretion and whose dysfunction leads to type 2 diabetes. The behavior of individual β-cells is heterogeneous and ranges from complete failure to secrete insulin to compensating with increased secretion. I will use the single-cell multi-omics approach to test the hypothesis that intracellular metabolism is the key to β-cell dysfunction, and analyze healthy and diabetic β-cells upon chemical exposure to establish i) their metabolic heterogeneity and differences, ii) variations and temporal dynamics in their metabolic behavior and iii) metabolic roadblocks that correlate with β-cell dysfunction. The single-cell multi-omics approach will open new horizons for understanding cellular heterogeneity, realizing cellular behavior that promotes health, and identifying treatment targets.

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