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. 2018 Nov 5;115(47):E11148–E11157. doi: 10.1073/pnas.1805436115

Fig. 9.

Fig. 9.

RGFP-966 rescues AD-like pathology in iPSC-derived AD-patient primary neurons. (A) RGFP-966 decreased HDAC3 activity in iPSC-AD neurons. (B) RGFP-966 decreased Aβ1–42 in iPSC-AD neurons. (C) In response to 10 μM RGFP-966, tau acetylation at lysine 280 (Ac-tau K-280) decreased significantly in patient 1, with no effect on tau phosphorylation at Ser202 and Ser396. (D) In response to 10 μM RGFP-966, tau phosphorylation at Ser202 and Ser396 decreased significantly in patient 2, with no effect on tau acetylation. Two-tailed unpaired t-test was used for analysis. The graphs represent mean ± SEM. *P < 0.05, **P < 0.01, ***P < 0.001, ****P < 0.001; n = 6.