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Resolution: standard / high Figure 5.
SNX5 is recruited to regions of the plasma membrane rich in PI(3,4)P2. (A) HEK-GFP-SNX5 cells were transfected with EGF-R and 24 h later serum-starved
overnight and either left untreated or treated with 100 ng/ml EGF for 3 min at 37°C,
as indicated. Cells were fixed and stained with anti-human EGF-R antibody followed
by Alexa568-conjugated goat anti-mouse IgG for detection of surface EGF-R. Optical
sections were taken to highlight the plasma membrane. Arrows indicate membrane ruffles
showing co-localization of GFP-SNX5 and EGF-R (B) HEK-GFP-SNX5 cells were transfected
with mCherry-TAPP1-PH and 24 h later serum-starved overnight then either left untreated
or treated with 100 ng/ml EGF for 5 min at 37°C and then fixed. Arrows indicate co-localization
of GFP-SNX5 and mCherry-TAPP1-PH (C) HEK-GFP-SNX5 cells were serum-starved overnight
and either left untreated or treated with 100 ng/ml EGF for 3 min at 37°C, in the
presence or absence of 100 nM AG1478, as indicated, and fixed. Boxed images are shown
magnified on upper right hand corner. (D). Cells from (C) were scored for plasma membrane
GFP-SNX5 by epifluorescence microscopy. 100 cells in triplicate were analysed. Shown
is mean and error bars represent standard deviation. *** p <0.005. Bars = 10 μm.
Lim et al. BMC Cell Biology 2008 9:58 doi:10.1186/1471-2121-9-58 |