(a)16 weeks APPPS1-21 mouse brain sections were stained
with Aβ/ApoE complexes (red) by PLA, methoxy X04 for Aβ plaque
(blue). High resolution confocal images show the spatial location of
Aβ-ApoE complexes and Aβ plaque in 3D view (lower panel). Bars
represent 10 µm. (b) Brain sections were stained with
methoxy-X04, ApoE, and LAMP1; the size of areas covered by methoxy-X04,
ApoE, and LAMP1 was determined. ApoE/X04 and LAMP1/X04 (X04 > 150
µm2) were quantified. n = 123 plaques from 4 control mice, 147
plaques from 5 treated mice. Bars 100 µm. (c) Aβ
plaque was stained with methoxy X04 (X04). Number of plaques per section and
number of plaque per area were quantified. control (n=4 mice), C5 (n=5). Bar
1000 µm; (d) Total plaque volume was determined in 3D,
plaques were further grouped according to the plaque volume. n = 71 random
fields from 4 control mice, 88 fields from 5 C5 treated mice. Bar 100
µm; (e) 8-week old C57BL6 brain cortex sections were
examined for the presence of C1q-ApoE complexes with methoxy X04. ApoE, or
C1q only antisera were used as negative controls. Bar represents 10
µm. Data in a,e are representative images from at least 3
biologically independent mouse samples. Data in b,c,d represent means
± SEM; two-tailed Student's t-test was applied to b,c,d; Two-way
ANOVA was applied to c,d.