Handling of cysteine S-conjugates of methylmercury in MDCK cells expressing human OAT1

Handling of cysteine S-conjugates of methylmercury in MDCK cells expressing human OAT1. Background. The activity of the organic anion transporter 1 (OAT1) has been implicated recently in the basolateral uptake of thiol conjugates of inorganic mercury in renal proximal tubular cells. However, very little is known about the role of OAT1 in the renal epithelial transport of organic forms of mercury, such as methylmercury (CH3Hg+), especially when it is in the form of the cysteine (Cys) S-conjugate of methylmercury (CH3Hg-Cys), which is believed to be a biologically relevant form of mercury. Methods. Accordingly, the present study, was designed to characterize the transport of CH3Hg-Cys in Madin-Darby canine kidney (MDCK) cells transfected stably with the human isoform of OAT1 (hOAT1) and in proximal tubular-derived NRK-52E cells. Results. Data on saturation kinetics, time dependency, substrate specificity, and temperature dependency demonstrate that CH3Hg-Cys is transported by hOAT1. Substrate-specificity data from the control cells also show that CH3Hg-Cys is a substrate of one or more transporter(s) that is/are not hOAT1. Additional findings indicate that at least one amino acid transport system is involved in the uptake of CH3Hg-Cys in MDCK cells. Furthermore, in the presence of cytotoxic concentrations of CH3Hg-Cys, rates of survival were lower in hOAT1-transfected cells than in wild-type control cells. Conclusion. The present data demonstrate clearly that CH3Hg-Cys is indeed a transportable substrate of OAT1. Moreover, the collective findings from the MDCK cells and NRK-52E cells infer that CH3Hg-Cys is a likely transportable mercuric species in proximal tubular epithelial cells that is taken up in vivo by both OAT1 and amino acid transporters.