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. Author manuscript; available in PMC: 2020 Feb 13.
Published in final edited form as: J Neurochem. 2019 Nov 4;152(2):235–251. doi: 10.1111/jnc.14898

Figure 6.

Figure 6.

RNAscope in situ hybridization (ISH) analysis of BACE1 transcriptional expression in the caudate and putamen from patients with AD (n=10) and age-matched controls (n=10). A: RNAscope in situ hybridization (ISH) labeling for BACE1 mRNA in the caudate and putamen from the AD subject included in the previous group of 5 representative subjects. Scale bar in the whole slide section: 10 mm. Scale bar in the high magnification mode Aβ plaque and NFT sections: 500 µm. Rectangle drawn in the whole slide section is magnified to highlight AB plaques and labeled as AD putamen image directly to the right. The numbers 1 and 2 designate the following regions: caudate (1) and putamen (2). B: Positive cells (red with arrow pointing to them) in the caudate and putamen of AD and control subjects with scale bar: 100 µm. C: semi-quantitative regional analysis of ISH signal in ROI, the signals were quantified as the average red dots count per mm2. Value shown are means ± SEM. T-test was used. A p value of < 0.05 was considered significant, *indicates p < 0.05 vs. the controls. D: BACE1 mRNA expression as density of D1R in the caudate and putamen from patients with AD and age-matched controls. rs, the Spearman’s rank correlation coefficient. The only significant correlation was in the caudate of the AD group (p = 0.02).