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Inside The NanoBreak Project

We study environmentally aged nanoplastics to understand their real-world composition and biological impact. NanoBreak combines realistic environmental materials, advanced human-relevant models and cutting-edge analytical tools to assess exposure pathways and health risks.

The Problem

Plastic pollution has become a global threat to ecosystems and human health. Beyond visible microplastics, there are even smaller particles: nanoplastics.

THE PROBLEM

Plastic pollution has become a global threat to ecosystems and human health. Beyond visible microplastics, there are even smaller particles: nanoplastics.

Due to their size, they can cross biological barriers, interact with proteins, lipids and DNA, and accumulate in key organs such as the liver or the brain. However, the most realistic and potentially hazardous forms — environmental nanoplastics and the chemicals they release — remain poorly understood.

Due to their size, they can cross biological barriers, interact with proteins, lipids and DNA, and accumulate in key organs such as the liver or the brain. However, the most realistic and potentially hazardous forms — environmental nanoplastics and the chemicals they release — remain poorly understood.

This lack of knowledge limits our ability to assess real-world risks and to design effective policies to protect human health and the environment.
We are open for collaborations, if you’re interested please contact This email address is being protected from spambots. You need JavaScript enabled to view it. Phd.

PROJECT INFO

ARIS STRATEGIC PROJECTS / GRAVITACIJA CALL 2024, PROJECT Nº 25-ARIS-STRP-01

FUNDING BY

SLOVENIAN RESEARCH AND INNOVATION AGENCY (ARIS)

PROJECT LEADER

MARTA SENDRA VEGA

AMOUNT FUNDING

2.500.000€

PROJECT DURATION

5 YEARS

AIMS and OBJECTIVES

To comprehensively understand the biological impacts of environmental nanoplastics (eNPs) and their leachates.

Specific Objectives (SOs)

  • SO1: To investigate the transformation, degradation, and metabolism of eNPs and their leachates in biological systems.
  • SO2: To assess the adaptive and resilient capacity under eNP and leachate exposure, considering intraspecific variability.
  • SO3: To study epigenetic and transgenerational modifications during the early developmental stage of zebrafish induced by eNPs exposure.
  • SO4: To integrate findings across zebrafish embryo and liver organoids for comparative toxicology induced by eNPs exposure.

Research Objectives (ORs)

  • RO1: Identification of metabolites and degradation pathways using spatial imaging; expanding knowledge about the biochemistry of leachates.
  • RO2: Generation of transcriptomic maps associated with adaptive capacity and resilience.
  • RO3: Identification of critical pathways for epigenetic and transgenerational damage.
  • RO4: Development of predictive toxicology frameworks linking eNP exposure to potential non-communicable diseases.

Specific Objectives (SOs)

  • SO1: To investigate the transformation, degradation, and metabolism of eNPs and their leachates in biological systems.
  • SO2: To assess the adaptive and resilient capacity under eNP and leachate exposure, considering intraspecific variability.
  • SO3: To study epigenetic and transgenerational modifications during the early developmental stage of zebrafish induced by eNPs exposure.
  • SO4: To integrate findings across zebrafish embryo and liver organoids for comparative toxicology induced by eNPs exposure.

Research Objectives (ORs)

  • RO1: Identification of metabolites and degradation pathways using spatial imaging; expanding knowledge about the biochemistry of leachates.
  • RO2: Generation of transcriptomic maps associated with adaptive capacity and resilience.
  • RO3: Identification of critical pathways for epigenetic and transgenerational damage.
  • RO4: Development of predictive toxicology frameworks linking eNP exposure to potential non-communicable diseases.

WORK PROGRAMME ORGANIZATION

WP1: Production and physico-chemical characterization of eNPs and its leachates (M1-M20)
  • Task 1.1: Selection of sampling locations and sampling (M1-M12)
  • Task 1.2: Classification and characterisation of eMPs (M3-M14)
  • Task 1.3: eNPs production from eMPS (M6-M14)
  • Task 1.4: Leachates production from eMPs and characterisation (M9-M20)
WP2: Innovative experimental models to support 3R principles (M6-M56)
  • Task 2.1: Advancing human liver organoids from hiPSCs: A platform for eNP toxicity studies (M6-M56)
  • Task 2.2: Zebrafish embryos to unveil the impact of eNPs (M12-M56)
  • Task 2.3: Models for induced liver injury in h-LO and zebrafish embryos to study resilience to eNPs exposure (M24-M56)
WP3:  High-Resolution Analysis of eNPs Interactions, Transformations, and Fate in Biological Systems (M16-M56)
  • Task 3.1:  Integrated Raman spectroscopy and NanoSIMS characterization of eNPs’ molecular interactions in biological systems (M16-M46)
  • Task 3.2: Investigating biomolecular interactions and toxicological impacts of eNPs (M26-M56)
WP4: A spatial multi-omics approach to investigate the impact of eNPs in Human Liver Organoids and Zebrafish Embryos; (M26-M58)
  • Task 4.1: Unravelling metabolic shifts: Spatial metabolomics of eNPs effects in h-LO and zebrafish embryos (M26-M50)
  • Task 4.2:  Decoding transcriptomic changes: Spatial transcriptomics of eNPs effects in h-LO and zebrafish embryos (M30-M54)
  • Task 4.3:  Mapping epigenetic changes: Spatial epigenomics of eNPs effects in h-LO and zebrafish embryos (M36-M58)
  • Task 4.4: Development of a pipeline for integrating metabolomic, transcriptomic, and epigenomic data to uncover comprehensive responses to eNPs (M26-M58)
WP5: Management and coordination; (M1-M60)
  • Task 5.1: Administrative and Financial Management (M1-M60)
  • Task 5.2: Scientific and Technical Management (M1-M60)
WP6: Dissemination, Exploitation and Communication; (M1-M60)
  • Task 6.1: Dissemination, Exploitation and Communication (DE&C) Strategy (M1-M60)  
  • Task 6.2: Data Management plan (M1-M60)
  • Task 6.3: IPR Management (M6-M60)
  • Task 6.4: Monitoring and Evaluation of DE&C Activities (M6-M60)

RELATED RESEARCH PROJECTS

PROJECT INFO

HORIZON EUROPE UNDER GRANT AGREEMENT N° 101244206

FUNDING BY

MARIE SKŁODOWSKA-CURIE ACTIONS (MSCA)

PROJECT LEADER

MARTA SENDRA VEGA

AMOUNT FUNDING

198.000€

PROJECT NAME

ENLIVEN

Description

Microplastics (MPs) have penetrated all the elements of our daily life, including the air we breathe and the food we consume. The risk increases when they break down into nanoscale plastics (NPs), as the smaller particles can enter cells and vital organs. While this poses threats to both ecology and human health, few studies focus on the long-term effects. In this context, the EU-funded ENLIVEN project uses human liver organoids and zebrafish embryos. ENLIVEN studies the effects of environmental nanoplastics (eNPs) on liver resilience and gene response to sensitise researchers to advanced nanotoxicology. It will map toxicological pathways, improve health risk prediction, and grow long-term capabilities in environmental health involving single-cell RNA sequencing and cutting-edge methodologies.

This project has been funded by Marie Skłodowska-Curie Actions (MSCA) Postdoctoral Fellowships, part of the EU’s research and innovation framework programme Horizon Europe under Grant Agreement N° 101244206

Objective

ENLIVEN is a research-through-training project designed to equip researcher with key expertise to tackle challenges in nanotoxicology. Plastic pollution has rapidly surpassed unprecedented in less than a century, with microplastics (MPs) found across various environments, ecosystems, and within the human body. MPs are present in the food we eat, the air we breathe, and the water we drink. While current analytical techniques limit the detection of nanoplastics (NPs <100 nm), plastic degradation continues beyond the microscale, leading to nanoscale interactions with potentially unknown consequences. NPs pose significant environmental and public health risks, particularly due to chronic exposure to harmful chemicals. Environmental nanoplastics (eNPs) are of particular concern due to their ability to penetrate cells and vital organs, increasing their retention in organisms. However, most research focuses on the environmental impact of MPs and NPs, leaving critical gaps in understanding their long-term effects on public health and biology. ENLIVEN aims to address this by uncovering the biological mechanisms of eNPs, examining their degradation, liver resilience, and long-term health impacts. Using human liver organoids and zebrafish embryos, ENLIVEN will study genes related to tolerance, sensitivity, and heritability, alongside liver resilience. The project proposes an innovative, integrative approach in predictive toxicology, combining bottom-up and top-down methodologies. It will link Adverse Outcome Pathways (AOP) through single-cell combinatorial RNA-seq and explore phenotypic variability via Drug-Induced Liver Injury studies in human liver organoids. This research will advance comparative human toxicology by revealing the biological mechanisms that respond to eNPs throughout life. Additionally, ENLIVEN will enhance researchers’ career prospects, foster international collaborations, and support the establishment of a research group at the home institution in Spain.