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. 2018 Mar 6;9(3):369. doi: 10.1038/s41419-018-0412-5

Fig. 5. ILC2-derived IL-9 protects MLEC from pyroptosis.

Fig. 5

a, b Representative flow cytometry plots and quantitation of Annexin V/7-AAD staining of MLEC cultured with LPS/TNFα and with or without rmIL-9 or rmIL-13 for 24 h. c, d Representative flow cytometry plots and quantitation of Annexin V/7-AAD staining of MLEC co-cultured with ILC2 (1 × 104 cells/well) and LPS (1 μg/ml) + TNFα (20 ng/ml) and with IgG or anti-IL-9 for 24 h. e, f Representative flow cytometry plots and quantitation of MLEC pyroptosis (caspase-1/TUNEL double-positive cells) with rmIL-9 (50 ng/ml), LPS, and TNFα for 24 h. g, h Representative flow cytometry plots and quantitation of Annexin V/7-AAD staining of MLEC from WT or Caspase-1−/− mice with LPS/TNFα for 24 h. MLECs were identified as CD31+ cells. Data shown are the mean ± SEM, n = 3–6 mice/group. *P < 0.05, **P < 0.01