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The effect of TTT on VEGFA and <t>CXCL12</t> expression (A) ELISA for serum levels of VEGFA and CXCL12. (B) qPCR for skin tissue expression of VEGFA and CXCL12. *, p < 0.05, **, p < 0.01, ***, p < 0.001 compared to the sham group or unilateral TTT group.
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Effects of preadministration of cyclosporine and cyclophosphamide on expression of MSC migration factors and EGFP-MSC engraftment. (A) Gene expression levels of Cxcl12 in rat renal cortex at days 1 (UUO day 1), 4 (UUO day 4), and 7 (UUO day 7) after UUO (n = 6 per group). (B and C) Western blotting analysis and quantification of SDF-1 in rat renal cortex at UUO day 1, UUO day 4, and UUO day 7. Protein levels of SDF-1 normalized to GAPDH ( n = 6 per group). Full-length blots are presented in . (D) Gene expression levels of Cxcl12 in rat renal cortex at UUO day 4 and same models with pre-administration of methylprednisolone (mPSL), cyclosporine (CyA), and cyclophosphamide (CP), respectively ( n = 6-7 per group). (E and F) Western blotting analysis and quantification of SDF-1 in rat renal cortex at UUO day 4 and same models with pre-administration of mPSL, CyA, and CP, respectively. Protein levels of SDF-1 normalized to GAPDH ( n = 6 per group). Full-length blots are presented in . (G–J) Representative immunofluorescence staining of EGFP in rat kidney sections and number of EGFP-positive cells per field at days 1 (MSC day 1), 3 (MSC day 3), and 5 (MSC day 5) after MSC administration (G and H; original magnification ×200, scale bar: 100 µm; n = 6 per group) and at MSC day 1 and MSC day 1 after preadministration of each immunosuppressive drug (I and J; original magnification ×200, scale bar: 100 µm; n = 6 per group). White arrows indicate EGFP-positive cells. (K) CXCR4 mRNA levels in EGFP-MSCs transfected with CXCR4 siRNA ( CXCR4 siRNA/EGFP-MSCs) or negative control siRNA (NC siRNA/EGFP-MSCs) ( n = 6 per group). (L and M) Representative immunofluorescence staining of EGFP in rat kidney sections and number of EGFP-positive cells per field at MSC day 1 after administration of CXCR4 siRNA/EGFP-MSCs or NC siRNA/EGFP-MSCs (original magnification ×200, scale bar: 100 µm; n = 7-8 per group). White arrows indicate EGFP-positive cells. Data are presented as mean ± S.D. # P < 0.01, * P < 0.05 versus sham group (A, C), UUO day 4 + PBS group (D, F), MSC day 1 group (H), MSC day 1 + PBS group (J), analyzed by one-way ANOVA followed by Bonferroni’s post hoc test, and analyzed by Student’s t test (K, M).

Journal: Stem Cells Translational Medicine

Article Title: Impact of immunosuppressive drugs on efficacy of mesenchymal stem cell therapy for suppressing renal fibrosis

doi: 10.1093/stcltm/szae073

Figure Lengend Snippet: Effects of preadministration of cyclosporine and cyclophosphamide on expression of MSC migration factors and EGFP-MSC engraftment. (A) Gene expression levels of Cxcl12 in rat renal cortex at days 1 (UUO day 1), 4 (UUO day 4), and 7 (UUO day 7) after UUO (n = 6 per group). (B and C) Western blotting analysis and quantification of SDF-1 in rat renal cortex at UUO day 1, UUO day 4, and UUO day 7. Protein levels of SDF-1 normalized to GAPDH ( n = 6 per group). Full-length blots are presented in . (D) Gene expression levels of Cxcl12 in rat renal cortex at UUO day 4 and same models with pre-administration of methylprednisolone (mPSL), cyclosporine (CyA), and cyclophosphamide (CP), respectively ( n = 6-7 per group). (E and F) Western blotting analysis and quantification of SDF-1 in rat renal cortex at UUO day 4 and same models with pre-administration of mPSL, CyA, and CP, respectively. Protein levels of SDF-1 normalized to GAPDH ( n = 6 per group). Full-length blots are presented in . (G–J) Representative immunofluorescence staining of EGFP in rat kidney sections and number of EGFP-positive cells per field at days 1 (MSC day 1), 3 (MSC day 3), and 5 (MSC day 5) after MSC administration (G and H; original magnification ×200, scale bar: 100 µm; n = 6 per group) and at MSC day 1 and MSC day 1 after preadministration of each immunosuppressive drug (I and J; original magnification ×200, scale bar: 100 µm; n = 6 per group). White arrows indicate EGFP-positive cells. (K) CXCR4 mRNA levels in EGFP-MSCs transfected with CXCR4 siRNA ( CXCR4 siRNA/EGFP-MSCs) or negative control siRNA (NC siRNA/EGFP-MSCs) ( n = 6 per group). (L and M) Representative immunofluorescence staining of EGFP in rat kidney sections and number of EGFP-positive cells per field at MSC day 1 after administration of CXCR4 siRNA/EGFP-MSCs or NC siRNA/EGFP-MSCs (original magnification ×200, scale bar: 100 µm; n = 7-8 per group). White arrows indicate EGFP-positive cells. Data are presented as mean ± S.D. # P < 0.01, * P < 0.05 versus sham group (A, C), UUO day 4 + PBS group (D, F), MSC day 1 group (H), MSC day 1 + PBS group (J), analyzed by one-way ANOVA followed by Bonferroni’s post hoc test, and analyzed by Student’s t test (K, M).

Article Snippet: Antibodies for α-SMA (Cat# A2547, Sigma-Aldrich), glyceraldehyde 3-phosphate dehydrogenase (GAPDH; Cat# G8795, Sigma-Aldrich), HMGB1 (Cat# ab79823, Abcam, Cambridge, UK), IFN-γ (Cat# ab133566, Abcam), and Stromal cell-derived factor-1/C-X-C motif ligand 12 (SDF-1/CXCL12; Cat# sc-74271, Santa Cruz Biotechnology, Santa Cruz, CA, USA) were used as primary antibodies, and horseradish peroxidase-conjugated goat anti-rabbit immunoglobulin G (Cat# P0448, Dako, Glostrup, Denmark) or goat anti-mouse immunoglobulin G (Cat# P0447, Dako) were utilized as secondary antibodies.

Techniques: Expressing, Migration, Western Blot, Immunofluorescence, Staining, Transfection, Negative Control

The effect of TTT on VEGFA and CXCL12 expression (A) ELISA for serum levels of VEGFA and CXCL12. (B) qPCR for skin tissue expression of VEGFA and CXCL12. *, p < 0.05, **, p < 0.01, ***, p < 0.001 compared to the sham group or unilateral TTT group.

Journal: Annals of Medicine

Article Title: Tibial transverse transport promotes wound healing in diabetic foot ulcers by stimulating endothelial progenitor cell mobilization and homing mediated neovascularization

doi: 10.1080/07853890.2024.2404186

Figure Lengend Snippet: The effect of TTT on VEGFA and CXCL12 expression (A) ELISA for serum levels of VEGFA and CXCL12. (B) qPCR for skin tissue expression of VEGFA and CXCL12. *, p < 0.05, **, p < 0.01, ***, p < 0.001 compared to the sham group or unilateral TTT group.

Article Snippet: Specifically, rabbit VEGFA ELISA kit (kl-deim-00300, Ke Lei Biological Technology Co., Ltd., Shanghai, China) and CXCL12 ELISA kit (CSB-E12656Rb, Cusabio, Wuhan, China) were assayed.

Techniques: Expressing, Enzyme-linked Immunosorbent Assay

Mechanism diagram of TTT promoting wound healing in DFUs (by figdraw). TTT induces wound fibroblasts to release VEGFA and CXCL12, thereby mediating EPC mobilization and homing, promoting angiogenesis and wound healing.

Journal: Annals of Medicine

Article Title: Tibial transverse transport promotes wound healing in diabetic foot ulcers by stimulating endothelial progenitor cell mobilization and homing mediated neovascularization

doi: 10.1080/07853890.2024.2404186

Figure Lengend Snippet: Mechanism diagram of TTT promoting wound healing in DFUs (by figdraw). TTT induces wound fibroblasts to release VEGFA and CXCL12, thereby mediating EPC mobilization and homing, promoting angiogenesis and wound healing.

Article Snippet: Specifically, rabbit VEGFA ELISA kit (kl-deim-00300, Ke Lei Biological Technology Co., Ltd., Shanghai, China) and CXCL12 ELISA kit (CSB-E12656Rb, Cusabio, Wuhan, China) were assayed.

Techniques: