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Investigation of the binding of Cr(III) complexes to bovine and human serum proteins: A proteomic approach
Author(s) -
Tkaczyk Cathy,
Huk Olga L.,
Mwale Fackson,
Antoniou John,
Zukor David J.,
Petit Alain,
Tabrizian Maryam
Publication year - 2010
Publication title -
journal of biomedical materials research part a
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.849
H-Index - 150
eISSN - 1552-4965
pISSN - 1549-3296
DOI - 10.1002/jbm.a.32700
Subject(s) - transferrin , chromium , fetal bovine serum , bovine serum albumin , blood proteins , u937 cell , internalization , albumin , cell culture , chemistry , microbiology and biotechnology , biochemistry , cell , materials science , biology , metallurgy , in vitro , genetics
Abstract Chromium (Cr) compounds are widely used in alloys manufacturing and forming processes. One of the main concerns in the use of cobalt‐chromium (Co‐Cr) alloy‐based implants is the long‐term fate of Co and Cr ions in the blood, organs, and urine of patients. Our previous studies have shown that Cr(III) forms complexes in different cell culture media, whereas Cr(VI) does not form any detectable structure under the same conditions. Because Cr(VI) is known to be more toxic than Cr(III), we hypothesized that the presence of serum proteins in the molecular structure of Cr(III) may be responsible for the difference in toxicity. We investigated the interaction of the Cr(III) complexes with serum proteins and their internalization by U937 macrophage‐like cells. By using a proteomic approach, we showed that in the presence of fetal bovine serum, Cr(III) complexes interacted only with albumin, whereas they interacted mainly with albumin, transferrin, and immunoglobulins (Ig) in the presence of human serum (HS). Cr(III) complexes were more easily engulfed by U937 macrophage‐like cells when they were formed with HS. To the best of our knowledge, this is the first report on the formation of Cr(III) complexes in the presence of serum proteins and the interaction of these complexes with U937 macrophage‐like cells. © 2010 Wiley Periodicals, Inc. J Biomed Mater Res, 2010