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Corning Life Sciences
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Image Search Results
Journal: Stem Cell Research & Therapy
Article Title: Ang II-AT2R increases mesenchymal stem cell migration by signaling through the FAK and RhoA/Cdc42 pathways in vitro
doi: 10.1186/s13287-017-0617-z
Figure Lengend Snippet: Effect of different concentrations of Ang II on migration of human bone marrow MSCs. a Nondirectional migration ability of human bone marrow MSCs after stimulations with different concentrations of Ang II (10 –8 , 10 –7 , 10 –6 , 10 –5 , and 3 × 10 –5 M) examined using the scratch assay. Wound sites (areas cleared of cells in the center of the scratched area) were observed and photographed at 0 and 24 h (200×). b Quantitative results of wound healing. c Directional migration ability of human bone marrow MSCs after stimulations with the different concentrations of Ang II indicated examined using the Transwell migration assay. Migrated cells on the bottom surfaces of the Transwell inserts were stained with crystal violet and observed under a microscope (200×). d Quantitative results of cell migration. n = 3; * p < 0.05 vs normal. Ang II angiotensin II
Article Snippet: Modified Boyden chamber assays were conducted using
Techniques: Migration, Wound Healing Assay, Transwell Migration Assay, Staining, Microscopy
Journal: Stem Cell Research & Therapy
Article Title: Ang II-AT2R increases mesenchymal stem cell migration by signaling through the FAK and RhoA/Cdc42 pathways in vitro
doi: 10.1186/s13287-017-0617-z
Figure Lengend Snippet: Effect of AT1R and AT2R antagonists on Ang II-mediated migration of MSCs. a Nondirectional migration ability of MSCs after stimulation with 100 nM Ang II following pretreatment with Losartan (5 μM) and/or PD-123319 (5 μM) examined with the scratch assay. Wound sites (areas cleared of cells in the center of the scratched area) were observed and photographed at 0 and 24 h (200×). b Quantitative results of wound healing. c Directional migration ability of MSCs after stimulation with 100 nM Ang II following pretreatment with Losartan (5 μM) and/or PD-123319 (5 μM) examined using the Transwell migration assay. Migrated cells on the bottom surfaces of the Transwell inserts were stained with crystal violet and observed under a microscope (200×). d Quantitative results of cell migration. Significant differences were found compared with the normal group ( n = 3; * p < 0.05) and compared with the control group ( n = 3; # p < 0.05). Ang II angiotensin II
Article Snippet: Modified Boyden chamber assays were conducted using
Techniques: Migration, Wound Healing Assay, Transwell Migration Assay, Staining, Microscopy, Control
Journal: Stem Cell Research & Therapy
Article Title: Ang II-AT2R increases mesenchymal stem cell migration by signaling through the FAK and RhoA/Cdc42 pathways in vitro
doi: 10.1186/s13287-017-0617-z
Figure Lengend Snippet: Roles of FAK and Rho GTPases in the migration of MSCs. a Nondirectional migration ability of MSCs after stimulation with Ang II and/or inhibitors of FAK and the Rho GTPases examined using the scratch assay. Wound sites (areas cleared of cells in the center of the scratched area) were observed and photographed at 0 and 24 h (200×). b Quantitative results of wound healing. c Directional migration ability of MSCs after stimulation with Ang II and/or inhibitors of FAK and the Rho GTPases examined using the Transwell migration assay. Migrated cells on the bottom surfaces of the Transwell inserts were stained with crystal violet and observed under a microscope (200×). d Quantitative results of cell migration. n = 3; * p < 0.05 vs normal, # p < 0.05 vs the control group. Ang II angiotensin II
Article Snippet: Modified Boyden chamber assays were conducted using
Techniques: Migration, Wound Healing Assay, Transwell Migration Assay, Staining, Microscopy, Control