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. 2022 Dec 13;12:21496. doi: 10.1038/s41598-022-25405-w

Figure 3.

Figure 3

Islet cell differentiation and characterization for insulin production in PARP1 control and deplete PANC-1 cells. (a) Phase contrast microscopic images of PANC-1 U6/SiP cells differentiated with control (SFM) and activin-A on day 10th. Color brightfield images show the presence of brick-red insulin staining with dithizone (DTZ) after differentiation. (b) Graph show quantification for islet-like clusters generated per field of an image from PANC-1 U6/SiP cells at day 10th differentiation. (c) Immunocytochemical characterization of generated clustered from PANC-1 U6/SiP cells for islet cell markers- insulin and glucagon (green). (d) Quantification for mean fluorescence intensity for human insulin production in differentiated U6 and SiP cells. Data represented as mean ± sem, p-value show significance at 95% confidence interval using two-way anova analysis compared to U6 cells (n = 3). (e) Quantification and modelling for presence of insulin in U6 vs SiP cells using 2-dimensional mean fluorescent intensity dot plot representation extracted from immunostained images with Axio-vision Zen 10 software, Zeiss, Canada, where insulin stays on Y-axis and dapi is marked on x-axis.