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Microelectrode array (MEA) platform as a sensitive tool to detect and evaluate Ostreopsis cf. ovata toxicity
Affiliation:1. ETT S.p.A., via Sestri 37, Genoa 16154, Italy;2. CNR-Institute of Biophysics (IBF), Via De Marini 6, 16149 Genoa, Italy;3. DiSTAV, University of Genoa, Corso Europa 26, 16132 Genoa, Italy;1. Department of Physics, Lanzhou University of Technology, Lanzhou 730050, China;2. College of Mechano-Electronic Engineering, Lanzhou University of Technology, Lanzhou 730050, China;1. Dipartimento di Chimica, Università degli Studi di Parma, Parco Area delle Scienze 17/A, 43124 Parma, Italy;2. Dipartimento di Bioscienze, Università degli Studi di Parma, Parco Area delle Scienze 11/A, 43124 Parma, Italy;3. Centro Interdipartimentale SITEIA.PR, Università degli Studi di Parma, Parco Area delle Scienze 181/A, 43124 Parma, Italy;1. Microchemistry and Microscopy Art Diagnostic Laboratory, University of Bologna, Via Guaccimanni 42, Ravenna 48121, Italy;2. Department of Chemistry “G. Ciamician”, University of Bologna, Via Selmi, Bologna 2 40126, Italy;1. Gene Therapy Center and Department of Ophthalmology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA
Abstract:In the last decade, the occurrence of harmful dinoflagellate blooms of the genus Ostreopsis has increased both in frequency and in geographic distribution with adverse impacts on public health and the economy. Ostreopsis species are producers of palytoxin-like toxins (putative palytoxin and ovatoxins) which are among the most potent natural non-protein compounds known to date, exhibiting extreme toxicity in mammals, including humans. Most existing toxicological data are derived from in vivo mouse assay and are related to acute effects of pure palytoxin, without considering that the toxicity mechanism of dinoflagellates can be dependent on the varying composition of complex biotoxins mixture and on the presence of cellular components.In this study, in vitro neuronal networks coupled to microelectrode array (MEA)-based system are proposed, for the first time, as sensitive biosensors for the evaluation of marine alga toxicity on mammalian cells. Toxic effect was investigated by testing three different treatments of laboratory cultured Ostreopsis cf. ovata cells: filtered and re-suspended algal cells; filtered, re-suspended and sonicated algal cells; conditioned growth medium devoid of algal cells. The great sensitivity of this system revealed the mixture of PTLX-complex analogues naturally released in the growth medium and the different potency of the three treatments to inhibit the neuronal network spontaneous electrical activity. Moreover, by means of the multiparametric analysis of neuronal network activity, the approach revealed a different toxicity mechanism of the cellular component compared to the algal conditioned growth medium, highlighting the potential active role of the first treatment.
Keywords:MEA-based testing assay  Toxins mixture
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