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Image Search Results
Journal: Experimental and Therapeutic Medicine
Article Title: Senescent hepatocytes enhance natural killer cell activity via the CXCL-10/CXCR3 axis
doi: 10.3892/etm.2019.8037
Figure Lengend Snippet: Cytokines in cell-free culture supernatants of senescent hepatocytes. (A) Representative images of cytokine arrays. 1, CCL-2; 2, CXCL-1; 3, CXCL-10. (B) Bar graph representing the densitometry of the spotted antibody array results. The secretion of IL-1α, IL-1β, IL-6, CCL-2, CXCL-1 and CXCL-2 was differentially increased. (C) ELISA analysis of CXCL-9, −10 and −11. The levels of only CXCL-10 exhibited significant augmentation. n=5. Data were analyzed by Student's t-test. **P<0.01. IL, interleukin; CCL, C-C motif chemokine ligand; CXCL, C-X-C motif chemokine ligand.
Article Snippet: Alternatively, DMEM/F12/10% FBS containing
Techniques: Ab Array, Enzyme-linked Immunosorbent Assay
Journal: Experimental and Therapeutic Medicine
Article Title: Senescent hepatocytes enhance natural killer cell activity via the CXCL-10/CXCR3 axis
doi: 10.3892/etm.2019.8037
Figure Lengend Snippet: Migration of NK cells in response to supernatants from senescent AML12 cells. Anti-CXCR3 or anti-CXCL-10 antibodies were used for the blocking assay. The percentage of NK cell migration was calculated by dividing the number of cells that migrated to the lower well by the total number of cells. n=3. Data were analyzed by one-way ANOVA with Tukey's post hoc test. ***P<0.001. NK, natural killer; CXCR, C-X-C motif chemokine receptor; CXCL, C-X-C motif chemokine ligand.
Article Snippet: Alternatively, DMEM/F12/10% FBS containing
Techniques: Migration, Blocking Assay
Journal: Cancer Cell International
Article Title: Tumor-associated macrophages derived CCL18 promotes metastasis in squamous cell carcinoma of the head and neck
doi: 10.1186/s12935-018-0620-1
Figure Lengend Snippet: CCL18 involves in M2-like TAMs induced EMT and stemness in SCCHN in vitro. Tu686 cells cultured with M2 CM or M0 CM in the presence or absence of an anti-CCL18 neutralizing antibody at 15 μg/mL, or an isotype-matched IgG protein. a – d qRT-PCR assays were used to check mRNA expression of EMT markers E-cadherin ( a ), Vimentin ( b ), and EMT transcription factors Snail ( c ) and Slug ( d ). e , f Representative images for tumorsphere formation and the number of tumorspheres. g , h mRNA expression of CSCs markers CD133 ( g ) and CD44 ( h ) was quantified by qPCR. Data are shown as mean ± SD. * P < 0.05, ** P <0.01, *** P < 0.001, **** P < 0.0001
Article Snippet: Cells were suspended in
Techniques: In Vitro, Cell Culture, Quantitative RT-PCR, Expressing