Department of Biomedical Engineering, Duff Medical Building, 3775 University Street, Montreal, Quebec H3A 2B4, Canada.
J Biomed Mater Res A. 2010 Jul;94(1):214-22. doi: 10.1002/jbm.a.32700.
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. (c) 2010 Wiley Periodicals, Inc. J Biomed Mater Res, 2010.
铬(Cr)化合物广泛应用于合金制造和成型过程。在使用钴铬(Co-Cr)合金基植入物时,主要关注的问题之一是患者血液、器官和尿液中 Co 和 Cr 离子的长期归宿。我们之前的研究表明,Cr(III)在不同的细胞培养基中形成配合物,而 Cr(VI)在相同条件下不会形成任何可检测到的结构。由于 Cr(VI)的毒性比 Cr(III)大,我们假设血清蛋白在 Cr(III)的分子结构中的存在可能是导致毒性差异的原因。我们研究了 Cr(III)配合物与血清蛋白的相互作用及其被 U937 巨噬细胞样细胞内化的情况。通过使用蛋白质组学方法,我们表明在胎牛血清存在的情况下,Cr(III)配合物仅与白蛋白相互作用,而在人血清(HS)存在的情况下,它们主要与白蛋白、转铁蛋白和免疫球蛋白(Ig)相互作用。Cr(III)配合物在与 HS 形成时更容易被 U937 巨噬细胞样细胞吞噬。据我们所知,这是首次报道在血清蛋白存在下形成 Cr(III)配合物以及这些配合物与 U937 巨噬细胞样细胞相互作用的研究。(c)2010 Wiley Periodicals, Inc. J Biomed Mater Res, 2010.