Fig. 3: Pancreas-resident macrophages play a predominant role in the development of MLD-STZ-induced diabetes. | Cell Death & Disease

Fig. 3: Pancreas-resident macrophages play a predominant role in the development of MLD-STZ-induced diabetes.

From: Loss of ubiquitin-conjugating enzyme E2 (Ubc9) in macrophages exacerbates multiple low-dose streptozotocin-induced diabetes by attenuating M2 macrophage polarization

Fig. 3: Pancreas-resident macrophages play a predominant role in the development of MLD-STZ-induced diabetes.The alternative text for this image may have been generated using AI.

WT and KO macrophage migration capacities were assessed in Transwell assays, and the cell numbers are shown in the bar graph a, scale bar: 50 μm. Wild-type (CD45.1) and KO (CD45.2) mice were used for parabiosis b. The proportions of CD45.1+ and CD45.2+ cells c in the peripheral blood were examined 2 weeks after surgical ligation. The percentages of CD45.1+ and CD45.2+ d cells in the CD11b+F4/80+ cell population from the ligated diabetic mouse pancreas 14 days after the initiation of STZ induction are shown in representative dot plots. The CD206+ macrophage subset of the resident macrophage population is shown in e. The frequency of CD206+ macrophages among migratory macrophages is shown in f. Results are means ± SEM from three mice per group and are representative of three similar experiments conducted. *P < 0.05; **P < 0.01; ***P < 0.001; and ns not significant.

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