Use of a combined effect model approach for discriminating between ABCB1- and ABCC1-type efflux activities in native bivalve gill tissue
Creators
- 1. CESAM & Departamento de Biologia, Universidade de Aveiro, 3810-193 Aveiro (Portugal)
- 2. Department of Environmental Chemistry, IDAEA-CSIC, Jordi Girona 18, 08034 Barcelona (Spain)
- 3. Department of Bioanalytical Ecotoxicology, UFZ — Helmholtz Centre for Environmental Research, Permoserstr. 15, D-04318 Leipzig (Germany)
- 4. Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch of Russian Academy of Sciences (SIPPB SB RAS), Lermontov Str. 132, 664033, Irkutsk (Russian Federation)
- 5. Institute of Hydrobiology, Dresden University of Technology, D-01062 Dresden (Germany)
Description
Aquatic organisms, such as bivalves, employ ATP binding cassette (ABC) transporters for efflux of potentially toxic chemicals. Anthropogenic water contaminants can, as chemosensitizers, disrupt efflux transporter function enabling other, putatively toxic compounds to enter the organism. Applying rapid amplification of cDNA ends (RACE) PCR we identified complete cDNAs encoding ABCB1- and ABCC1-type transporter homologs from zebra mussel providing the molecular basis for expression of both transporter types in zebra mussel gills. Further, efflux activities of both transporter types in gills were indicated with dye accumulation assays where efflux of the dye calcein-am was sensitive to both ABCB1- (reversin 205, verapamil) and ABCC1- (MK571) type specific inhibitors. The assumption that different inhibitors targeted different efflux pump types was confirmed when comparing measured effects of binary inhibitor compound mixtures in dye accumulation assays with predictions from mixture effect models. Effects by the MK571/reversin 205 mixture corresponded better with independent action, whereas reversin 205/verapamil joint effects were better predicted by the concentration addition model indicating different and equal targets, respectively. The binary mixture approach was further applied to identify the efflux pump type targeted by environmentally relevant chemosensitizing compounds. Pentachlorophenol and musk ketone, which were selected after a pre-screen of twelve compounds that previously had been identified as chemosensitizers, showed mixture effects that corresponded better with concentration addition when combined with reversine 205 but with independent action predictions when combined with MK571 indicating targeting of an ABCB1-type efflux pump by these compounds. - Highlights: • Sequences and function of ABC efflux transporters in bivalve gills were explored. • Full length Dreissena polymorpha abcb1 and abcc1 cDNA sequences were identified. • A mixture effect design with inhibitors was applied in transporter activity assays. • ABCB1- and ABCC-type efflux activities were distinguished in native gill tissue. • Inhibitory action of environmental chemicals targeted ABCB1-type efflux activity.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.taap.2016.02.020Additional details
Identifiers
- DOI
- 10.1016/j.taap.2016.02.020;
- PII
- S0041-008X(16)30042-4;
Publishing Information
- Journal Title
- Toxicology and Applied Pharmacology
- Journal Volume
- 297
- Journal Page Range
- p. 56-67
- ISSN
- 0041-008X
- CODEN
- TXAPA9
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 49036940
- Subject category
- S60: APPLIED LIFE SCIENCES;
- Descriptors DEI
- ABUNDANCE; ANIMAL TISSUES; ATP; BINARY MIXTURES; GILLS; GLYCOPROTEINS; KETONES; MUSSELS; POLYMERASE CHAIN REACTION; TOXICITY
- Descriptors DEC
- ANIMALS; AQUATIC ORGANISMS; BODY; CARBOHYDRATES; DISPERSIONS; GENE AMPLIFICATION; INVERTEBRATES; MIXTURES; MOLLUSCS; NUCLEOTIDES; ORGANIC COMPOUNDS; PROTEINS; RESPIRATORY SYSTEM; SACCHARIDES
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.