FIGURE

Fig. 4

ID
ZDB-FIG-240206-75
Publication
Ye et al., 2023 - RNF213 loss-of-function promotes pathological angiogenesis in moyamoya disease via the Hippo pathway
Other Figures
All Figure Page
Back to All Figure Page
Fig. 4

Endothelial RNF213 knockdown promotes HBMEC proliferation, migration and angiogenesis. (A) Two designed siRNA/shRNA sequences were used to mimic RNF213 loss-of-function conditions, which were confirmed by western blot (siNC versus siRNF213 #1: n = 4, 1.00 ± 0.00 versus 0.43 ± 0.05, P = 0.0286; siNC versus siRNF213 #2: n = 4, 1.00 ± 0.00 versus 0.42 ± 0.03, P = 0.0286) and qRT-PCR analyses (siNC versus siRNF213 #1: n = 4, 1.00 ± 0.03 versus 0.45 ± 0.04, P = 0.0286; siNC versus siRNF213 #2: n = 4, 1.00 ± 0.03 versus 0.45 ± 0.02, P = 0.0286). (B) The siRNF213-treated human brain microvascular endothelial cells (HBMECs) showed greater cell viability than the siNC-treated HBMECs at 48 h (n = 6, 0.47 ± 0.03 versus 0.52 ± 0.05, P = 0.0931) and also showed significantly greater cell viability at 72 h (n = 6, 0.93 ± 0.07 versus 1.09 ± 0.06, P = 0.004) based on the results of CCK-8 assays. (C) A BrdU incorporation assay was conducted to measure the proliferation of siNC- and siRNF213-treated HBMECs. The siRNF213-treated HBMECs showed a significantly greater BrdU incorporation ratio than the siNC-treated HBMECs (n = 5, 2.09 ± 0.47 versus 9.84 ± 1.89%, P = 0.0079). Scale bar = 20 µm. (D) Flow cytometry was used to assess the proliferation of siNC- and siRNF213-treated HBMECs after labelling with EdU and Hoechst 33342. The siRNF213-treated HBMECs showed a significantly greater cell proliferation ratio than the siNC-treated HBMECs (n = 4, 69.75 ± 6.07 versus 93.15 ± 0.62%, P = 0.0286). (E) Transwell assays were performed to measure vertical HBMEC migration. siRNF213-treated HBMECs showed greater vertical migration than siNC-treated HBMECs (n = 6, 86.25 ± 38.92 versus 124.75 ± 57.69, P = 0.0152). Scale bar = 100 µm. (F) A wound healing assay was used to measure horizontal HBMEC migration. The siRNF213-treated HBMECs showed markedly greater horizontal migration than the siNC-treated HBMECs at 24 h (n = 5, 16.16 ± 6.44 versus 55.45 ± 9.20, P = 0.0079) and 48 h (n = 5, 49.76 ± 5.26 versus 73.36 ± 14.78, P = 0.0079). Scale bar = 100 µm. (G) A tube formation assay was performed to measure HBMEC angiogenesis. AngioTool software was used to automatically detect the vessel length (red) and junctions (green). Scale bar = 100 µm. (H) The siRNF213-treated HBMECs showed significantly greater vessel area (n = 5, 1.00 ± 0.16 versus 1.59 ± 0.36, P = 0.0079), vessel density (n = 5, 1.00 ± 0.17 versus 1.58 ± 0.36, P = 0.0079), vessel length (n = 5, 1.00 ± 0.16 versus 1.63 ± 0.42, P = 0.0079), total number of junctions (n = 5, 1.00 ± 0.22 versus 2.56 ± 1.13, P = 0.0079), junction density (n = 5, 1.00 ± 0.23 versus 2.54 ± 1.12, P = 0.0079), and branching index values (n = 5, 1.00 ± 0.18 versus 1.22 ± 0.09, P = 0.0317) than the siNC-treated HBMECs. Each dot represents one sample. The means ± SDs are shown. The dashed line indicates the region of interest. *P < 0.05, **P < 0.01, ***P < 0.001 and ****P < 0.0001.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
This image is the copyrighted work of the attributed author or publisher, and ZFIN has permission only to display this image to its users. Additional permissions should be obtained from the applicable author or publisher of the image. Full text @ Brain