Implementation of X-ray microscopy and micro-XANES analysis for investigations of the cellular uptake and cellular metabolism of transition metals

被引:9
作者
Dillon, CT [1 ]
Kennedy, BJ
Lay, PA
Lai, B
Cai, Z
Stampfl, APJ
Ilinski, P
Legnini, D
Maser, J
Rodrigues, W
Shea-McCarthy, G
Cholewa, M
机构
[1] Univ Sydney, Sch Chem, Ctr Heavy Metals Res, Sydney, NSW 2006, Australia
[2] Argonne Natl Lab, Expt Facil Div, Argonne, IL 60439 USA
[3] Australian Nucl Sci & Technol Org, Div Phys, Menai, NSW 2234, Australia
[4] Brookhaven Natl Lab, Upton, NY 11973 USA
[5] Gesell Schwerionenforsch mbH, D-64291 Darmstadt, Germany
来源
JOURNAL DE PHYSIQUE IV | 2003年 / 104卷
关键词
D O I
10.1051/jp4:200300083
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Micro-SRIXE (synchrotron-radiation-induced X-ray emission) and micro-XAS (X-ray absorption spectroscopy) were used to probe the uptake of exogenous metals by cells. The high flux and the sub-micron resolution of the hard X-ray microprobe, offer the experimenter the ability to obtain highly sensitive spatial and structural information of cellular elements. In this work the uptake of carcinogenic Cr(VI) was compared with that of a relatively non-toxic Cr(III) complex by micro-SRIXE mapping of whole cells. High intracellular Cr concentrations were observed in Cr(VI)-treated cells, while no significant Cr uptake was observed for Cr(Ill)-treated cells, as is consistent with uptake studies performed by other techniques. Micro-XANES analysis of Cr(V)- and Cr(VI)-treated cells showed that the predominant oxidation product following cellular metabolism was Cr(III). As shown by X-ray microscopic analysis of thin-sectioned cells, however, the reduction of Cr(VI) to Cr(III) did not occur at a fast enough rate to exclude Cr entry into the cell nucleus.
引用
收藏
页码:293 / 296
页数:4
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