ALUMINUM AND ALZHEIMERS-DISEASE - SITES OF ALUMINUM BINDING IN HUMAN NEUROBLASTOMA-CELLS DETERMINED USING AL-26 AND ACCELERATOR MASS-SPECTROMETRY

被引:14
作者
KING, SJ
TEMPLAR, J
MILLER, RV
DAY, JP
DOBSON, CB
ITZHAKI, RF
FIFIELD, LK
ALLAN, GL
机构
[1] UNIV MANCHESTER, DEPT CHEM, MANCHESTER M13 9PL, LANCS, ENGLAND
[2] UNIV MANCHESTER, INST SCI & TECHNOL, DEPT OPTOMETRY, MANCHESTER M60 1QD, LANCS, ENGLAND
[3] AUSTRALIAN NATL UNIV, DEPT NUCL PHYS, CANBERRA, ACT 2600, AUSTRALIA
基金
英国惠康基金;
关键词
D O I
10.1016/0168-583X(94)96056-9
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
The aluminium distribution between the major cell compartments of human neuroblastoma cells grown in culture has been determined using Al-26 and accelerator mass spectrometry (AMS). Cells (IMR-32) were grown for eight days in a culture medium containing Al-EDTA (0.2mM) spiked with Al-26, harvested, and fractionated by standard biochemical techniques. Al-26 in fractions after ashing to Al2O3 was determined by AMS using the 14UD accelerator at ANU Canberra. The cytoplasmic and nuclear cell compartments appeared to have reached diffusive equilibrium with the culture medium. Whilst Al-26 was retained by the nuclear proteins and nuclear sap, Al-26 did not appear to bind to the nucleic acids (DNA/RNA).
引用
收藏
页码:469 / 472
页数:4
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