Aluminum is present in many manufactured foods and medicines and is added t
o drinking water for purification purposes. Tt has been proposed that alumi
num is a contributing factors to several neurodegenerative disorders such a
s Alzheimer's disease. However, this remains controversial primarily due to
the unusual properties of aluminum and a lack of information on its cellul
ar sites of action. To resolve some of these questions, we have examined al
uminum uptake in both neuronal and astroglial cells as well as the role of
metal speciation. The relative accumulation of four aluminum salts, aluminu
m maltolate, aluminum lactate, aluminum chloride and aluminum fluoride, was
investigated and correlated with cell viability and intracellular distribu
tion as determined by morin staining. Significant differences in aluminum i
ncorporation and toxicity were observed in both neuronal and glia cells wit
h the largest effects exhibited by the maltol species. This was accompanied
by a nuclear accumulation in the neuronal cell line that was contrasted by
the perinuclear, vesicular distribution in astrocytes that partially co-lo
calized with cathepsin D, a lysosomal marker. These findings demonstrate di
fferences in aluminum species and highlights the importance of these factor
s in modulating the toxic effect of aluminum. (C) 2000 Elsevier Science B.V
. All rights reserved.