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. Author manuscript; available in PMC: 2022 Sep 1.
Published in final edited form as: J Immunol. 2021 Aug 4;207(5):1419–1427. doi: 10.4049/jimmunol.2100266

Figure 2.

Figure 2.

Sirpα−/− mice display enhanced macrophage inflammatory responses in MLDS-induced type I diabetes. WT and Sirpα−/− mice were administered STZ (25 mg/kg) for 5 consecutive days (marked by purple lines and arrows). Hyperglycemia was considered when serum glucose >200 mg/dl in two consecutive tests. A) Blood glucose level (left) and frequency of hyperglycemic mice (right). B) Immunofluorescent staining of pancreatic islets showing CD11b+ leukocyte infiltration (green) and β cell loss (determined by insulin labeling, red) in non-diabetic and diabetic WT and Sirpα−/− mice on d20. C) Flow cytometry analysis of CD11b+ leukocytes and CD11b+CD86+ M1 macrophages recovered from pancreatic islets of diabetic WT and Sirpα−/− mice. Data in each panel represent at least three independent experiments. **, P < 0.01. ***, P < 0.001.