z-logo
Premium
Reciprocal inhibition of Cd and Pb sulfocomplexes for uptake in Caco‐2 cells
Author(s) -
Aduayom I.,
Jumarie C.
Publication year - 2005
Publication title -
journal of biochemical and molecular toxicology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.526
H-Index - 58
eISSN - 1099-0461
pISSN - 1095-6670
DOI - 10.1002/jbt.20085
Subject(s) - chemistry , cadmium , metal , biophysics , biochemistry , microbiology and biotechnology , biology , organic chemistry
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 Cd 2+ and chlorocomplex (CdCl   n 2− n ) species. Here we show 1.9 times higher uptake levels for 109 CdCl   n 2− ncompared to 210 PbCl   n 2− n . Reciprocal inhibitions of chlorocomplexes were observed with a much higher inhibitory effect of Cd compared to Pb. Replacing Cl − by NO   3 −increased both the level of aquo ion 109 Cd 2+ and 109 Cd accumulation. In contrast, higher levels of 210 Pb 2+ did not favor 210 Pb uptake. For both metals, higher uptake data were recorded in the presence of SO 4 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 Cd 2+ (but not Pb 2+ ), sulfocomplexes of both metals would preferentially be taken up compared to chlorocomplexes. NRAMP2 is not involved in Pb 2+ uptake, and the NRAMP2‐mediated Cd 2+ 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. © 2005 Wiley Periodicals, Inc. J Biochem Mol Toxicol 19:256–265, 2005; Published online in Wiley InterScience ( www.interscience.wiley.com ). DOI 10.1002/jbt.20085

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom