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Image Search Results
Journal: Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
Article Title: The lysosomal trafficking regulator is necessary for normal wound healing
doi: 10.1111/wrr.12984
Figure Lengend Snippet: Assessment of protein levels in conditioned media from primary fibroblast culture. (A) Representative blots of relevant cytokines, chemokines, and growth factors from RayBiotech Mouse Cytokine Antibody Arrays demonstrating WT and Bg fibroblasts’ relative protein secretion in conditioned media. Fibroblasts lines were derived from 2 to 3 mice from each genotype and experiments were done with 3–5 technical replicates. (B) Quantification of the integrated densities (n = 3 per group). Integrated densities are relative to manufacturer controls. Relative integrated densities of MCP-1, IGF-1, and IGFBP-2 were significantly decreased in Bg samples (p = 0.0083, p = 0.0159, and p = 0.0111, respectively). (C) Confirmatory ELISAs of MCP-1 and IGFBP-2 (n = 5 per group) show decreased protein secretion from Bg fibroblasts (p = 0.0068 and p = 0.0498, respectively). *p ≤ 0.05, **p ≤ 0.01
Article Snippet: Taqman Fast Advanced Master Mix (Cat# 4444557,
Techniques: Derivative Assay
Journal: Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
Article Title: The lysosomal trafficking regulator is necessary for normal wound healing
doi: 10.1111/wrr.12984
Figure Lengend Snippet: Protein localization and gene expression in fibroblasts. (A) LAMP-1 immunofluorescent (IF) images of WT and Bg fibroblasts demonstrate enlarged lysosomes in Bg fibroblasts. (B) RT-qPCR analysis shows no change in relative gene expression of lysosomal trafficking regulator (LYST) between WT and Bg fibroblasts. (C) MCP-1 staining shows primarily cytoplasmic staining of similar degree between genotypes. (D) Gene expression of MCP-1 is comparable between genotypes at all time points. (E) Representative images of IGF-1 also show high nuclear localization with presence in nucleoli in both genotypes. (F) IGF-1 gene expression between cell types is similar at 24 and 48 h. At 72 h, Bg cells show a higher degree of gene expression (p = 0.0156). (G) Representative IF images of IGFBP-2 show a high degree of nuclear localization in both genotypes. (H) Relative gene expression of IGFBP-2 is decreased in Bg fibroblasts at 24 h (p = 0.0083) but is comparable to WT cells starting at 48 h. Fibroblasts lines were derived from 2 to 3 mice from each genotype and experiments were done with 5–6 technical replicates. DAPI was used to visualise nuclei (blue). Actin is represented with green, and proteins of interest are red. Scale bar = 20 μm. *p ≤ 0.05, **p ≤ 0.01 (n = 5–6 per group)
Article Snippet: Taqman Fast Advanced Master Mix (Cat# 4444557,
Techniques: Gene Expression, Quantitative RT-PCR, Staining, Derivative Assay
Journal: Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society
Article Title: The lysosomal trafficking regulator is necessary for normal wound healing
doi: 10.1111/wrr.12984
Figure Lengend Snippet: Localization of IGF associated proteins in fibroblasts. (A) Co-stain of IGF-1 (red) and IGFBP-2 (green) shows nuclear colocalization (yellow) of the proteins based on the microscopic resolution (0.24 μm). Colocalization is not seen in the cytoplasm or in the nucleoli of the nucleus. (B) IGF-1 (red) and IGF-1 receptor (IGF-1R) (green) do not appear to colocalize. IGF-1R appears mostly cytoplasmic. (C) Lysosomes stained with LAMP-1 (red) and IGF-1R (green) show colocalization associated with the membrane of lysosomes. DAPI (blue) is used to visualise nuclei and void regions in nuclei are nucleoli. Scale bar = 20 μm
Article Snippet: Taqman Fast Advanced Master Mix (Cat# 4444557,
Techniques: Staining, Membrane