Figure 1
Figure 1. Localized necrotic cell death in Rb-null fetal liver. (A-B) TUNEL immunohistochemistry on sagittal sections of wild-type and Rb-null E13.5 fetal liver. (C-D) Representative flow cytometric analysis of annexin-V and TER119 staining on disaggregated whole E13.5 fetal liver from wild-type (C, 7.1% ± 0.6%, P < .002) and Rb-null (D, 2.8% ± 1.0%, P < .002) embryos to detect phosphotidyl serine externalization. (E-G) TUNEL staining for DNA fragmentation of wild-type (E) and Rb-null (F-G) E13.5 fetal livers (1000× magnification). The arrow in panel E identifies a phagocytic macrophage and s indicates a liver sinusoid. The dorsal region of the Rb-null fetal liver (F) shows markedly less TUNEL positivity than the ventral end of the liver that is distant from the hepatic vasculature. (H-J) Protein blue staining of sections of E13.5 wild-type fetal liver (H), more dorsal, healthy regions of the Rb-null fetal liver (I), and dying regions in the ventral end of the Rb−/− fetal liver (J) with black arrows indicating the presence of phagocytic macrophages and red arrows indicating distended, remnant nuclei. See ″Fluorescence microscopy and island counts″ for image acquisition information.

Localized necrotic cell death in Rb-null fetal liver. (A-B) TUNEL immunohistochemistry on sagittal sections of wild-type and Rb-null E13.5 fetal liver. (C-D) Representative flow cytometric analysis of annexin-V and TER119 staining on disaggregated whole E13.5 fetal liver from wild-type (C, 7.1% ± 0.6%, P < .002) and Rb-null (D, 2.8% ± 1.0%, P < .002) embryos to detect phosphotidyl serine externalization. (E-G) TUNEL staining for DNA fragmentation of wild-type (E) and Rb-null (F-G) E13.5 fetal livers (1000× magnification). The arrow in panel E identifies a phagocytic macrophage and s indicates a liver sinusoid. The dorsal region of the Rb-null fetal liver (F) shows markedly less TUNEL positivity than the ventral end of the liver that is distant from the hepatic vasculature. (H-J) Protein blue staining of sections of E13.5 wild-type fetal liver (H), more dorsal, healthy regions of the Rb-null fetal liver (I), and dying regions in the ventral end of the Rb−/− fetal liver (J) with black arrows indicating the presence of phagocytic macrophages and red arrows indicating distended, remnant nuclei. See ″Fluorescence microscopy and island counts″ for image acquisition information.

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