Reciprocal inhibition of Cd and Pb sulfocomplexes for uptake in Caco-2 cells.

J Biochem Mol Toxicol

Département de Chimie, Université du Québec à Montréal, C.P. 8888, Succ. centre-ville, Montréal, Québec, Canada H3C 3P8.

Published: November 2005

Cadmium-lead interactions for uptake were studied in the TC7 clone of human enterocytic-like Caco-2 cells as a function of inorganic metal speciation. We have previously shown that Cd uptake in these cells involves both the free cation Cd2+ and chlorocomplex (CdCln(2-n)) species. Here we show 1.9 times higher uptake levels for 109CdCln(2-n) compared to 210PbCln(2-n). Reciprocal inhibitions of chlorocomplexes were observed with a much higher inhibitory effect of Cd compared to Pb. Replacing Cl- by NO3- increased both the level of aquo ion 109Cd2+ and 109Cd accumulation. In contrast, higher levels of 210Pb2+ did not favor 210Pb uptake. For both metals, higher uptake data were recorded in the presence of SO4(2-), leading to sulfocomplex formation, compared with Cl-. Reciprocal inhibitions were minimal at high-cation levels but were significant and comparable in the presence of sulfo-complexes. We conclude that, in addition to Cd2+ (but not Pb2+), sulfocomplexes of both metals would preferentially be taken up compared to chlorocomplexes. NRAMP2 is not involved in Pb2+ uptake, and the NRAMP2-mediated Cd2+ uptake is insensitive to Pb. Uptake of Pb chlorocomplexes could involve specific mechanisms but of very low affinity, whereas uptake of Pb sulfocomplexes occurs with high affinity.

Download full-text PDF

Source
http://dx.doi.org/10.1002/jbt.20085DOI Listing

Publication Analysis

Top Keywords

uptake
10
caco-2 cells
8
higher uptake
8
reciprocal inhibitions
8
reciprocal inhibition
4
inhibition sulfocomplexes
4
sulfocomplexes uptake
4
uptake caco-2
4
cells cadmium-lead
4
cadmium-lead interactions
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!