-
A
Representative confocal pictures of double immunostaining with CD31 (red) and PDGFRα (green) on Control and Cripto
My‐LOF TA sections at day 5 after injury. Split green and red channels of Fig
7E are shown.
-
B
Representative pictures of triple immunostaining with VEcad (red), KLF4 (green), and pSMAD3 (white) on Control and Cripto
My‐LOF TA sections at day 5 after injury. Merged channels of VEcad/KLF4 (top panels) and VEcad/pSMAD3 of Fig
7H are shown.
-
C, D
Representative pictures of double immunostaining with VEcad (red) and KLF4 (green) on Control and CriptoMy‐LOF TA sections at day 2 (C, left panels) and day 3 (D, left panels) after injury and quantification of VEcad/KLF4 double‐positive cells per area (mm2) at day 2 (C, right panel) and day 3 (D, right panel).
Data information: Nuclei were counterstained with DAPI (blue). Scale bar: 100 μm. Confocal pictures (A) scale bar: 25 μm. Magnification of the boxes is 3.5×. Data are expressed as box plots displaying minimum, first quartile, median, third quartile, and maximum (
n ≥ 5 biological replicates;
P = ns; Student's
t‐test).