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. 2011 Jul 11;286(36):31852–31863. doi: 10.1074/jbc.M111.244335

FIGURE 1.

FIGURE 1.

Aβ induces β2AR degradation in vivo and in vitro. A, the endogenous β2AR in cerebral tissues from wild type (WT) and presenilin 1/amyloid precursor protein (PS1/APP) double transgenic mice were examined with Western blot and quantified. n = 6; **, p < 0.01, versus control by unpaired t test. IP, immunoprecipitate. B, HEK293 cells expressing FLAG-tagged human β2AR were stimulated with either Aβ (10−6 m) or isoproterenol (Iso, 10−7 m) for 4 h. The remaining biotin-labeled β2ARs were isolated and blotted, and the Western blots (WB) were quantified. n = 6; **, p < 0.01 versus control by one-way ANOVA. C, HEK293 cells expressing FLAG-β2AR were stimulated with Aβ (10−6 m) or isoproterenol (10−7 m) for 40 min, and cells were costained with anti-FLAG and anti-Lamp I antibodies.