Pt. Xu et al., Sialylated human apolipoprotein E (apoE(s)) is preferentially associated with neuron-enriched cultures from APOE transgenic mice, NEUROBIOL D, 6(1), 1999, pp. 63-75
Mice transgenic for human APOE2, E3, and E4 alleles express native 34-kDa h
uman apoE and two sialylated apoE isoproteins with approximate molecular we
ights of 37 kDa (apoE(s)) and 39 kDa (apoE(s2)) in brain. These multiple ap
oE/apoE(s)/apoE(s2) band patterns on Western blot are also observed in huma
n brain, but are not seen in wild-type mouse brain. Both the 37-kDa apoE(s)
and 39-kDa apoE(s2) are coprecipitated with native 34-kDa apoE by antibody
to human apoE. Neuraminidase digestion eliminates the 37- and 39-kDa forms
and results in a downward shift in the bands to the position of the 34-kDa
native form. These sialylated apoE isoproteins are found preferentially as
sociated with neurons and contribute significantly (50-60%) to the total ne
uronal apoE in neuronal cultures from transgenic mice, while only 5-10% of
total apoE is sialylated in cultures enriched in glial cells. In situ hybri
dization and immunocytochemistry demonstrate apoE mRNA and apoE immunoreact
ivity are predominantly located in cell soma of neurons, not in neuronal pr
ocesses. (C) 1999 Academic Press.