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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The article proposes a novel in vitro method for the rapid and sensitive assessment of the toxicity and ecotoxicity of pollutants, based on the motility of Mytilus galloprovincialis hemocytes. The method aims to contribute to the development of more ethical and sensitive toxicological and ecotoxicological exposure tests.

Abstract

Hemocytes are the circulating immune-competent cells in bivalve mollusks and play a key role in several important functions of cell-mediated innate immunity. During the early stages of the immune response, hemocytes actively migrate to the site of infection. This inherent motility is a fundamental characteristic of these cells. It represents a key cellular function that integrates multiple processes, such as cell adhesion, cell signaling, cytoskeletal dynamics, and changes in cell volume. Therefore, alterations in cell motility following exposure to drugs or pollutants can serve as a useful toxicological endpoint. Despite the fundamental role of cell motility in cellular physiology, it has been poorly investigated from a toxicological perspective. This work proposes a novel in vitro method for the rapid and sensitive assessment of the toxicity and ecotoxicity of pollutants, based on evaluating the hemocyte motility of Mytilus galloprovincialis. We developed a cell motility assay on hemocytes adhering to the bottom of a 96-well polystyrene microplate. Following exposure to increasing concentrations of drugs, cell trajectories, and velocities were quantified by cell tracking under time-lapse microscopy, allowing us to measure the effects on hemocyte motility. Due to the ease of hemocyte collection from the animals in a relatively non-invasive manner, the proposed method offers an alternative test for screening the effects and mechanisms of action of pollutants and drugs. It aligns with the 3Rs (Replacement, Reduction, and Refinement) criteria, addressing ethical concerns and contributing to the reduction of vertebrate in vivo animal testing.

Introduction

Effect-based methods, such as in vitro and in vivo bioassays, represent innovative tools for the detection of the effects of environmental chemical pollutants in living organisms and for their use as tools in environmental monitoring and risk assessment1,2,3,4. They complement the classical analytical chemical approach by overcoming some of its limitations. For instance, effect-based methods can assess the bioavailability of pollutants, their impact on organism health, and the combined toxicological effects of mixtures. The....

Protocol

All experiments were performed under the Italian Animal Welfare legislation (D.L.26/2014) that implemented the European Committee Council Directive (2010/63 EEC). Mytilus galloprovincialis is a filter-feeding bivalve, commonly known as the Mediterranean mussel. It is native to the Mediterranean Sea and the Atlantic coast of southern Europe. It was introduced and is widespread in Western North America, Asia, and South Africa. It is an important commercial fishery species in several parts of the world. The details.......

Representative Results

The study introduces a novel in vitro method for quickly and sensitively assessing the toxicity and ecotoxicity of pollutants, utilizing the motility of Mytilus galloprovincialis hemocytes. Figure 1A-C shows representative time-lapse imaging of hemocytes after 30 min attachment to the bottom of the well. The cells in the figure were stained with Neutral Red just before the motility assessment. Cell movements were monitored using optical mic.......

Discussion

The protocol described in this work represents a novel in vitro method suitable for the rapid and sensitive assessment of the toxicity of drugs and pollutants based on evaluating the motility of M. galloprovincialis hemocytes and its alterations. Motility is a peculiar aspect of the immune function of these cells21,22,23,37,38, therefore any .......

Acknowledgements

This research was funded by the project "Dipartimento di Eccellenza" awarded to DiSTeBA by the Italian Ministry of University and Research, CUP: F85D18000130001, and by NBFC (National Biodiversity Future Center) funded by European Union NextGenerationEU, PNRR, project n. CN00000033. We also thank BIOforIU infrastructure at the Department of Biological and Environmental Sciences and Technologies of the University of Salento.

....

Materials

NameCompanyCatalog NumberComments
0.2 µm filter (diameter 25 mm)ABLUO labware
2.5 ml hypodermic syringe needdle 22GRays2522CM32labware
96-well flat-bottom polystyrene TC-treated microplateCorning3916labware
CaCl2.2H2OMerk (Sigma - Aldrich) C3881-1KGChemical
Chemotaxis and Migration Tool software (Ibidi GmbH)software
Cytation 5 Agilent BioTeckCytation 5Equipment: Cell imaging multimode reader
Dimethyl sulfoxide (DMSO) Merk (Sigma - Aldrich) 472301Solvent
Falcon 15 mL Tube Conical BottomCorning352196labware
H3BO3Merk (Sigma - Aldrich) B0394Chemical
Hemocytometer Fast read 102BiosigmaBVS100labware
HEPES (4-(2-hydroxyethyl)-1-piperazine-ethanesulfonic acid)Merk (Sigma - Aldrich) H3375-500GChemical
ImageJ softwareNIHsoftware
KBrMerk (Sigma - Aldrich) P9881Chemical
KClMerk 104936Chemical
L-glutamineMerk (Sigma - Aldrich) G7513Essential amino acid for cell culture medium
MgCl2·6H2OMerk (Sigma - Aldrich) M2670Chemical
MgSO4Merk (Sigma - Aldrich) M7506Chemical
Microscope Nikon Eclipse E600NikonEquipment: Cell imaging 
Na2SO4Riedel-de Haen31481Chemical
NaClMerk (Sigma - Aldrich) 31434-1KG-RChemical
NaFFluka71519 500gChemical
NaHCO3Merk (Sigma - Aldrich) S5761-1KGChemical
Neutral RedMerk (Sigma - Aldrich) N4638-1GVital cell dye
Penicillin/StreptomycinMerk (Sigma - Aldrich) P0781-100MLAntibiotics for cell culture
SrCl2·6H2OMerk (Sigma - Aldrich) 255521Chemical
Trypan blue Merk (Sigma - Aldrich) T8154Cell dye

References

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