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. 2017 Jan 27;8(12):18914–18923. doi: 10.18632/oncotarget.14835

Figure 2. IL-17B prompted the proliferation and migration of MSCs.

Figure 2

(A) Cell-counting assay for the proliferating ability of hucMSCs and GC-MSCs treated with/without 200 ng/ml rIL-17B for 48 hours. (B) Western blot analyses of Cyclin-D3 protein expression in hucMSCs and GC-MSCs treated with/without 100 ng/ml and 200 ng/ml rIL-17B for 48 hours. (C) The migratory ability of hucMSCs and GC-MSCs treated with/without 100 ng/ml and 200 ng/ml rIL-17B for 12 hours was evaluated by the Transwell® migration assay. All samples were measured in triplicate, ***p < 0.001.