Review
Copyright ©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Jul 14, 2014; 20(26): 8491-8504
Published online Jul 14, 2014. doi: 10.3748/wjg.v20.i26.8491
Figure 1
Figure 1 Immunohistochemical staining of Indian hedgehog in normal liver and after up-regulation of β-catenin signalling. Ihh protein was detected in liver sections of wild type (WT) mice (A) and mice with down-regulated expression of APC protein after three month of age (B). Ihh protein in WT mice shows a clear gradient which is highest in hepatocytes surrounding the central veins. After up-regulation of β-catenin signalling the zone of Ihh-positive hepatocytes is considerably extended as are other known pericentral markers (e.g., glutamine synthetase; c.f.[8,42]). Sections were stained with Rabbit anti-mouse Ihh polyclonal antibody (Abcam) followed by the EnVision® + Dual Link System-horse radish peroxidase (DAKO) and counterstained with hemalum (Mayer solution).
Figure 2
Figure 2 Scheme illustrating aspects of zonation of central metabolism in normal mice. Selected functions of central metabolism are depicted as conical boxes showing the direction of their porto-central gradients with specific emphasis of the strength of this gradient in the glutamine synthetase-positive zone (right of the vertical line). Dashed boxes indicate gradients that have been determined using a single method only (proteome analysis), instead of at least two independent methods (other boxes). Since the data is valid for normal mice, the presumably corresponding gradient of Wnt/β-catenin signalling is depicted at the top of the scheme, above the row of the hepatocytes. PP: Periportal; PC: Pericentral.