Research
Studies at the interface between organism and environment
Making use of in vitro models of the gill and the intestinal epithelia we want to understand how fish respond to environmental and man-made stressors.
Such in vitro models allow a mechanistic approach to tackle physiology and toxicology questions.
Research Interests
Essential Trace Elements Homeostasis
Essential metals, like for example Copper, Zinc and Iron, are necessary for all living organisms to thrive. The interaction between metals and living organisms is at the very base of the origin of life on our planet. It is intriguing that protein domains involved in the homeostasis of essential metals, used by the cell as structural or catalytic cofactors of proteins, are highly conserved from bacteria to humans. Several proteins are involved in the tight regulation of intracellular metal concentration and distribution that is defined as metal homeostasis. The study of this sophisticated machinery at the molecular level will ultimately help us understand how organisms acclimate and adapt to multiple environmental stressors including metals.
Environmental Biomonitoring
Environmental bio-monitoring using primary fish gill cell culture system (FIGCS). When grown on transwells, primary gill cells develop a polarized tight epithelia that tollerate direct exposure with unfiltered river water. Therfore FIGCS represents an ideal system to determine the bioavailability of water pollutants.
Nanotoxicology
Understaning nanoparticle-cell interactions is key in order to address mechanisms of toxicity of nanoparticles. In vitro models of epithelial barriers will be instrumental in understanding exposure scenarios and effects of nanoparticles at the cellular and molecular level.
Fish Physiology and Nutrition
- Fish and amphibian larvae can absorb essential trace metals from two routes of exposure from the water via the gill and from the diet via the gut.
- Interplay between macro- and micro- elements homeostasis.
- Interplay between essential trace elements and lipid metabolism.