FIGURE

Figure 1

ID
ZDB-FIG-250109-272
Publication
Dai et al., 2024 - Hyperaminoacidemia from interrupted glucagon signaling increases pancreatic acinar cell proliferation and size via mTORC1 and YAP pathways
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Figure 1

IGS increases acinar cell proliferation and cell size

(A and C) Representative images of acinar tissue immunofluorescence of amylase (green) and Ki67 (red). DAPI (blue) was used to label the nuclei. The pancreas sections were from Gcg+/+ or Gcg−/− mice (A) or from C57BL/J6 mice treated with IgG or GCGR-Ab (C).

(B and D) Quantification of Ki67 positive acinar cell (n = 5–7). Arrows point to Ki67+ cells.

(E) Representative immunofluorescent images of pancreas sections from 18 dpf zebrafish. Green (GFP), red (EdU), and blue (Amylase). Arrows, EdU+ acinar cells.

(F) Quantification of EdU-positive acinar cells (n = 12).

(G and I) Representative images of acinar tissue immunofluorescence of Amylase (Green), E-cadherin, and Collagen (Red). DAPI (blue) was used to label the nuclei. The pancreas sections were from Gcg+/+ or Gcg−/− mice (G) or from C57BL/J6 mice treated with IgG or GCGR-Ab (I).

(H and J) Measurements of acinar cell size (by area) in the two mouse models.

(K) Average acinar cell size of control and gcgr−/− zebrafish. Each data point is the average of more than 50 cells from one fish. Scale bar, 15 μm in (E). Scale bar, 50 μm in others. Data are represented as mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001. Student’s t test.

Expression Data

Expression Detail
Antibody Labeling
Phenotype Data

Phenotype Detail
Acknowledgments
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