Dysregulation
of lipid trafficking upon Calcrl depletion. (A–D)
Representative oil red O stained sections
of tamoxifen-treated Calcrlfl/fl and Calcrlfl/fl/Prox1-CreERT2 animals
after HFD challenge. Arrows highlight lipid deposits in enterocytes,
and arrowheads mark lipid at the center of villi. Boxed regions are
displayed as digitally zoomed insets on the right of each image. (E–H)
Representative fluorescent images of Podoplanin and E-cadherin stained
sections of tamoxifen Calcrlfl/fl and Calcrlfl/fl/Prox1-CreERT2 animals
after BODIPY gavage. Arrows indicate BODIPY droplets. Boxed regions
are displayed as digitally zoomed insets on the right of each image.
(I–L) Representative fluorescent images of LYVE1 and PECAM-stained
sections of tamoxifen Calcrlfl/fl and Calcrlfl/fl/Prox1-CreERT2 animals
after BODIPY gavage. Arrows indicate BODIPY droplets, arrowheads highlight
BODIPY accumulation within LECs, asterisk shows PECAM-labeled blood
vessels, and “L” marks the lacteal lumen. Boxed regions
are displayed as digitally zoomed insets on the right of each image.
(M–P) Representative transmission electron microscopy images
of tamoxifen Calcrlfl/fl and Calcrlfl/fl/Prox1-CreERT2 lacteals after
HFD challenge. Arrowheads indicate lipid droplets, red brackets highlight
adherens junctions, and “L” marks the lacteal lumen.
Boxed regions are displayed as digitally zoomed insets on the right
of each image. (Q–T) Representative fluorescent images of LYVE1
and APOA1 stained sections of tamoxifen Calcrlfl/fl and Calcrlfl/fl/Prox1-CreERT2 animals after BODIPY gavage. Arrowheads highlight APOA1 chylomicron
accumulation within LECs or within the lacteal lumen. For all panels
in Figure 3: N = 4–6 animals per genotype. Scale bars: 100 μm
in (A, C); 50 μm in (E, G, I, K); 1 μm in (M, O).