Fig. 5: In situ imaging of circSCMH1 in mouse brain sections. | Nature Communications

Fig. 5: In situ imaging of circSCMH1 in mouse brain sections.

From: Fast and sensitive multivalent spatial pattern-recognition for circular RNA detection

Fig. 5

A Schematic diagram of the experimental design for in situ imaging circSCMH1 in mouse brain sections. Created in BioRender. Yao, H. (2024) BioRender.com/w93y687. B Colocalization of NeuN and circSCMH1 in mouse brain sections after incubation with TDF sensor for 3, 6, and 12 h. Green, NeuN; Red, circSCMH1; Blue, DAPI. Scale bar, 20 μm. C Quantification of circSCMH1 intensity in neurons. Data are presented as mean ± SEM, n = 4 slices (selected 10 representative cells in each slice for quantification) from 4 mice/group. ***P < 0.001 versus 3 h, ###P < 0.001 versus 6 h using one-way ANOVA followed by Holm–Sidak post hoc multiple comparison test. D Schematic diagram of the experimental design for in situ imaging circSCMH1 in PT mouse brain sections. Created in BioRender. Yao, H. (2024) BioRender.com/w93y687. E Colocalization of NeuN and circSCMH1 in brain sections of Sham and PT mice after incubation with TDF sensor for 12 h. Green, NeuN; Red, circSCMH1; Blue, DAPI. Scale bar, 20 μm. F Quantification of circSCMH1 intensity in neurons. Data are presented as mean ± SEM, n = 4 slices (selected 10 representative cells in each slice for quantification) from 4 mice/group. ***P < 0.001 versus Sham group using unpaired two-tailed Student’s t test. G The procedure of in situ imaging using biotin-labeled probes. H The procedure of in situ imaging using TDF sensors. I Representative images of the colocalization of NeuN and circSCMH1 in mouse brain sections using biotin-labeled probes and TDF sensors respectively. Green, circSCMH1; Red, NeuN; Blue, DAPI. Scale bar, 20 μm. J The plots were the analysis of circSCMH1 intensity, circSCMH1+ cells/mm2, and signal-to-noise ratio in neurons. Data are presented as mean ± SEM, n = 4 slices (selected 10 representative cells in each slice for quantification) from 4 mice/group for the analysis circSCMH1 intensity, circSCMH1+ cells/mm2, and signal-to-noise ratio. ***P < 0.001 versus biotin-labeled probes using unpaired two-tailed Student’s t test. WT wild type, PT photothrombotic, LSCM laser scanning confocal microscope. Source data are provided as a Source Data file.

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