Journal: Journal of neurochemistry
Article Title: Rotenone affects p53 transcriptional activity and apoptosis via targeting SIRT1 and H3K9 acetylation in SH-SY5Y cells.
doi: 10.1111/jnc.13172
Figure Lengend Snippet: Fig. 5 Neuroprotection of resveratrol in a cellular model of Parkinson’s disease (PD) is SIRT1-dependent. Western blot (a) and quantification (b) of SIRT1 and p53 protein levels after siRNA transfection. (c) qRT- PCR assay to test SIRT1 and p53 changes on mRNA levels. Data are presented as mean SD. *p < 0.05 as compared to mock group (a); **p < 0.01 as compared to mock (a).
Article Snippet: Rotenone and resveratrol affects apoptosis in SH-SY5Y cells To evaluate the neurotoxicity of rotenone in SH-SY5Y cells, we first treated cells with rotenone at various concentrations Rabbit anti-human Bax Cell Signaling Technology WB (1 : 1000) Rabbit anti-human Bcl-2 Cell Signaling Technology WB (1 : 1000) Rabbit anti-human p53 Cell Signaling Technology WB (1 : 1000) Rabbit anti-human ac-p53 Cell Signaling Technology WB (1 : 1000) Rabbit anti-human SIRT1 Cell Signaling Technology WB/IP (1 : 1000) Mouse anti-human H3K9-me3 Cell Signaling Technology ChIP (1 : 1000) Mouse anti-human H3K9-ac Cell Signaling Technology ChIP (1 : 1000) Mouse anti-human b-actin Cell Signaling Technology WB (1 : 1000) Rabbit anti-human AMPK Cell Signaling Technology WB (1 : 1000) Rabbit anti-human p-AMPK Cell Signaling Technology WB (1 : 1000) © 2015 International Society for Neurochemistry, J. Neurochem. (2015) 134, 668--676 (0, 0.1, 1, 10, 100 lM) for 24 h, or at 1 lM for different time periods (0, 3, 6, 12, 24, 36 h).
Techniques: Western Blot, Transfection, Quantitative RT-PCR