a Schematic of AAV-BR1-FTO administration and staining analysis. b, c Representative images with CD31 staining showing blood vessels in the peri-infarct cortex at day 28 after PT in mice, followed by the analysis of vascular area fraction, total vascular length, and the number of branches. n = 6 mice/group. Scale bars, 100 μm (overview), 20 μm (insets). ***P < 0.0001 (vascular area, numbers of branches), ***P = 0.0001 (vascular length) versus sham + AAV-BR1-Con; ##P = 0.0075 (vascular area), ##P = 0.0071 (vascular length), ###P < 0.0001 (numbers of branches) versus PT + AAV-BR1-Con. d Representative images and quantification of newly generated BrdU+/CD31+ endothelial cells at day 28 after PT. n = 6 mice/group. Scale bars, 20 μm. *P = 0.0101 versus sham + AAV-BR1-Con; ###P < 0.0001 versus PT + AAV-BR1-Con. e Representative images and quantification of CD13+ pericyte coverage on CD31+ microvessels in the peri-infarct cortex at day 28 after PT. Scale bars, 20 μm. n = 6 mice/group. **P = 0.0054 versus the sham+AAV-BR1-Con group; #P = 0.0485 versus PT + AAV-BR1-Con. f Representative images obtained by using LEDs at λ = 570 nm for the HBT at day 4, 7, 14, 21, and 28 after PT in Ftoflox/flox cKI mice with AAV-BR1-Con or AAV-BR1-Cre, followed by 2D reconstruction and analysis of branch area fraction using Imaris x64 9.0.0. n = 3 mice/group. Scale bars, 100 μm (overview), 20 μm (insets). *P = 0.0112 (14d), **P = 0.0027 (21d), **P = 0.0019 (28d) versus AAV-BR1-Con. The data in c–e were expressed as mean ± SEM; two-way ANOVA followed by Bonferroni’s post hoc multiple comparison tests. The data in f were expressed as mean ± SEM; two-way repeated-measures ANOVA followed by Holm–Sidak post hoc multiple comparison test. Components of this figure were created using Servier Medical Art templates, which are licensed under a Creative Commons Attribution 3.0 Unported License; https://smart.servier.com. Source data are provided as a Source Data file. AAV adeno-associated virus, cKI conditional knock-in, Con control, ITR inverted terminal repeat, LSL loxP-STOP-loxP, Pre pre-injury, WPRE woodchuck hepatitis virus post-transcriptional regulation.