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. 2020 Jul 9;10(18):8298–8314. doi: 10.7150/thno.46934

Figure 1.

Figure 1

ATF6 is upregulated in SAP pancreatic tissues from patients and PRSS1 transgenic (PRSS1Tg) mice accompanying with elevated apoptosis. (A) ATF6 expression was assessed by immunohistochemistry. (B) The localization and expression of ATF6 were examined by immunoelectron microscopy (IEM); black arrows (↑): representative gold nanoparticles. (C) Histological alterations, myeloperoxidase (MPO) activity, acinar cell apoptosis, and microstructural changes in pancreatic tissues from human and PRSS1Tg mice were assessed by hematoxylin and eosin (H&E) staining, immunohistochemistry, terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) assays and transmission electron microscopy (TEM) as indicated. black arrows (↑): cell nuclei; white arrows (↑): endoplasmic reticula; blue arrows (↑): zymogen granules; purple arrows (↑): mitochondria; red arrows (↑): apoptotic bodies. (-), not treated with caerulein; (+), treated with caerulein. The data are presented as the means ± SDs; * p ≤ 0.05, ** p ≤ 0.01, *** p ≤ 0.001. Scale bars = 100 µm.