Article Figures & Data
Figures
- Fig. 1.
Class 2 amphiphiles inhibit intracellular cholesterol transport and decrease β-cleavage of APP in neuronal cells. SH-SY5Y cells (A) or mature rat cortical neurons in culture (B) were labeled with14C-cholesterol in LDL for 2–12 hr (A) or 24 hr (B).14C-cholesterol ester formation in cells incubated in the presence or absence of 3 μg/ml (for neuroblastoma cells) or 0.75 μg/ml (for primary neurons) U18666A or 80 μm imipramine was monitored by the extraction of lipids and subsequent TLC. Depicted are densitometric quantifications of 14C-cholesterol ester signal intensities as a percentage of the total 14C activity per lane (means from three experiments). CE, Cholesterol ester; Chol, cholesterol. C, SFV-infected mature rat cortical neurons were incubated for 8 hr with LDL at different concentrations of U18666A. Conditioned medium was immunoprecipitated with W02, followed by Western blot detection with W02. Immunoprecipitations of conditioned media from neurons exposed to LDL and either 0.75 μg/ml U18666A (+) or not (−) with antibodies G2-10 or G2-11 were detected with G2-10 to visualize secretory Aβ40 and p3 or with W02 for the detection of secretory Aβ42, respectively.D, Western blot of respective neuronal lysates with W02 (after W02 immunoprecipitation), anti-calnexin antibody, or antibody 95.23 against PS1 NTF. C, D, Quantifications of intracellular (ic) and secreted (sec) APP, βCTF, and overall Aβ levels (n = 4–7 experiments). Depicted are ratios of signal intensities from U18666A- or imipramine-treated versus untreated primary cortical neurons or SH-SY5Y cells. Error bars indicate 1 SD.
- Fig. 2.
U18666A increases intracellular and secretory Aβ levels in SP-C99-transfected SH-SY5Y cells. Human SH-SY5Y neuroblastoma cells stably transfected with APP C-terminal fragment SP-C99 were incubated for 24 hr with 50 μg/ml LDL in the presence (+) or absence (−) of 3 μg/ml U18666A. Conditioned medium (A) and cell lysates (B) were immunoprecipitated with antibody W02, followed by Western blot detection with W02. Graphs show quantification of intracellular (ic) and secreted (sec) endogenous APP, C99, and overall Aβ levels (n = 5 experiments). Depicted are ratios of signal intensities from U18666A-treated versus untreated cells. Error bars indicate 1 SD. C, Medium and lysates of SH-SY5Y cells were immunoprecipitated with antibodies G2-10 and G2-11 specific for Aβ40 and Aβ42, respectively, and were detected with W02. Western blots with W02 show effects of U18666A treatment on secretory and intracellular Aβ species compared with C99.
- Fig. 3.
Inhibiting intracellular cholesterol transport induces an accumulation of PS1 in vesicular compartments associated with late endosomes and lysosomes. Human SH-SY5Y neuroblastoma cells were incubated for 24 hr with 50 μg/ml LDL in the presence (E–H) or absence (A–D) of 3 μg/ml U18666A. After fixation in paraformaldehyde the cells were triple labeled with polyclonal PS1 antibody 95.23 (A, E;green fluorescence), monoclonal antibody Osw2 to v-ATPase as a late endosomal/lysosomal marker (B, F;red fluorescence), and filipin for the detection of cellular cholesterol (C, G; bluefluorescence). Parental CHO-25RA cells (with regular sterol distribution) and CHO-CT43 cells (expressing a nonfunctional NPC1 protein) were incubated with 50 μg/ml LDL for 24 hr, fixed with paraformaldehyde, and triple labeled with PS1 antibody 95.23 (I, M), filipin (K, O), and the monoclonal antibody 6C4 against LBPA to visualize late endosomes (J, N; red fluorescence). D, H, L, P, Merged images. Arrows indicate selected regions positive for all three markers. Scale bars, 10 μm.
- Fig. 4.
PS-containing compartments are positive for Rab7 and surround late endosomes in a ring-like manner. SH-SY5Y (A–C) or A431 cells (D–L) were incubated for 24 hr with 50 μg/ml LDL and 3 μg/ml U18666A. After fixation in paraformaldehyde the SH-SY5Y cells were stained against PS1 (A, C; green) and v-ATPase (B, C; red). Fixed A431 cells stably overexpressing Rab7-GFP (E, H, K;green) were labeled with a monoclonal PS1 antibody (D, F; red), polyclonal PS2 antibody (G, I; red), or Oil red O to visualize neutral lipids (J, L; red). C, F, I, L, Merged images. Scale bars, 8 μm. Arrowsindicate selected vesicles positive for both markers.Insets show single sections from confocal stacks of random vesicular structures in cell bodies. Scale bars ininsets, 1 μm.
- Fig. 5.
Rab7-containing compartments after U18666A exposure of hippocampal neurons are distinct from cholesterol-retaining late endosomes and retain Aβ42 and PS1. Mature hippocampal neurons were incubated with LDL and U18666A for 24 hr, fixed, and stained with filipin (B, E;red) and either monoclonal antibody 6C4 against LBPA (A, C; green) or a polyclonal antibody against Rab7 (D, F; green). G, H, Coimmunostainings of 95.23 for PS1 and monoclonal antibody G2-11 to detect cellular Aβ42. A–C andinsets in D–I show areas in the cell body of a hippocampal neuron. C, Merged image fromA, B. F, Merged image from D, E. I, Merged image from G, H. Arrows indicate selected compartments. Scale bars, 4 μm.
- Fig. 6.
PS1-bearing vesicular compartments in hippocampal neurons impaired in cholesterol transport exclude β′COP and BiP but retain calnexin. Fully polarized rat hippocampal neurons in culture were incubated with 50 μg/ml LDL and 0.75 μg/ml U18666A for 24 hr. Neurons were fixed and triple labeled with antibody 95.23 (A, E, I), filipin (C, G, K), and monoclonal antibodies against β′COP (B), BiP/GRP78 (F), or calnexin (J). D, H, L, Merged images. Bottom insets show selected regions of single sections in the cell body of the depicted neuron (top insets). Arrows indicate selected compartments. Scale bars, 3 μm.
- Fig. 7.
U18666A decreases cholesterol ester formation independently of PS1 expression. Cultured mouse fibroblasts from wild-type (PS1+/+PS2+/+), PS1 single knock-out (PS1−/−PS2+/+), and PS1/PS2 double knock-out (PS1−/−PS2−/−) mice were labeled with14C-cholesterol in LDL in the presence (+) or absence (−) of 3 μg/ml U18666A for 24 hr. Lipids were extracted and separated by TLC. Effects of U18666A on CE formation in treated cells at equal CE levels in untreated cells are shown.
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