Arsenic transport by zebrafish aquaglyceroporins
Arsenic is one of the most ubiquitous toxins and endangers the health of tens of millions of humans worldwide. It is a mainly a water-borne contaminant.
Trivalent arsenic (AsIII) is one of the major species that exists environmentally. The transport of AsIII has been studied in microbes, plant and mammals.
Members of aquaglyceroporins family have been shown to actively conduct AsIII and its organic metabolite, monomethylarsenite (MAsIII). However, the transport in any fish species has not been characterized.
Results: In this study, five members of the aquaglyceroporin family from zebrafish (Danio rerio) were cloned, and their ability to transport water, glycerol, and trivalent arsenicals (AsIII and MAsIII) and antimonite (SbIII) was investigated.
Genes for at least seven aquaglyceroporins have been annotated in the zebrafish genome project. Here, five genes which are close homologues to human AQP3, AQP9 and AQP10 were cloned from a zebrafish cDNA preparation.
These genes were named aqp3, aqp3l, aqp9a, aqp9b and aqp10 according to their similarities to the corresponding human AQPs. Expression of aqp9a, aqp9b, aqp3, aqp3l and aqp10 in multiple zebrafish organs were examined by RT-PCR.
Our results demonstrated that these aquaglyceroporins exhibited different tissue expression. They are all detected in more than one tissue.
The ability of these five aquaglyceroporins to transport water, glycerol and the metalloids arsenic and antimony was examined following expression in oocytes from Xenopus leavis. Each of these channels showed substantial glycerol uptake at equivalent rates.
These aquaglyceroporins also facilitate uptake of inorganic trivalent arsenite (AsIII), organic monomethylarsenite (MAsIII) and trivalent antimonite (SbIII) in a mercury regulatory manner. Arsenic accumulation in fish larvae and in different tissues from adult zebrafish was studied following short-term arsenic exposure.
The results showed that liver is the major organ of arsenic accumulation; other tissues such as gill, eye, heart, intestine muscle and skin also exhibited significant ability to accumulate arsenic. The zebrafish larvae also accumulate considerable amounts of arsenic.
Conclusion: This is the first molecular identification of fish arsenite transport systems and we propose that the extensive expression of the fish aquaglyceroporins and their ability to transport metalloids suggests that aquaglyceroporins are the major pathways for arsenic accumulation in a variety of zebrafish tissues.
Uptake is one important step of arsenic metabolism. Our results will contribute to a new understanding of aquatic arsenic metabolism and will support the use of zebrafish as a new model system to study arsenic associated human diseases.
Author: Mohamad HamdiMarco SanchezLauren BeeneQianyong LiuScott LandfearBarry RosenZijuan Liu
Credits/Source: BMC Molecular Biology 2009, 10:104
Published on: 2009-11-25
Copyright by the authors listed above - made available via BioMedCentral (Open Access). Please
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