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Image Search Results
Journal: Frontiers in Immunology
Article Title: Sex-dependent differences in type I IFN-induced natural killer cell activation
doi: 10.3389/fimmu.2023.1277967
Figure Lengend Snippet: Type I IFN subtypes modulate natural killer cells in-vitro . Changes (presented as deltaΔ) in (A) activation measured by CD69+ expression on NK cells, and in (B) degranulation measured by CD107a+ expression on NK cells. Representative dot plots are shown on right side for CD69+ (A) and CD107a+ (B) expression on NK cells. PBMCs were stimulated with respective Type I IFN subtypes for 4h followed by a degranulation assay for 5h with K562 cell line. Plotted percentage delta values were calculated by subtracting the corresponding unstimulated condition with K562 cell co-cultures from each experiment. (C) Spearman correlation coefficient (r) between delta changes in activation (CD69) and delta changes in degranulation (CD107a) of NK cells after IFN-stimulation. Paired t test; non parametric Wilcoxon test; n=10. Spearman correlation; 100 XY pairs. *p<0.05; **p<0.005.
Article Snippet: NK cells were isolated from PBMCs using
Techniques: In Vitro, Activation Assay, Expressing, Degranulation Assay
Journal: Frontiers in Immunology
Article Title: Sex-dependent differences in type I IFN-induced natural killer cell activation
doi: 10.3389/fimmu.2023.1277967
Figure Lengend Snippet: Sex differences in NK cell activation after TLR7/8 stimulation. (A, B) Poly-IFNα ELISA quantification of supernatants after overnight stimulation with 1ug/mL TLR7/8 agonist (CL097) of male and female-derived PBMCs (A) and pDCs (B) . Average of duplicates are represented in box and whisker plots, n=13 (A) and n=12 (B) . Mann-Whitney test. (C) Representation of transwell co-culture system. Overnight culture of NK cells, plated in upper chamber, with stimulated or unstimulated PBMCs or pDCs, plated in lower chamber. Image created with BioRender.com . (D, E) Relative activation levels measured by CD69+ NK cells normalized to their corresponding control condition (untreated). NK cells were cultured with control stimulation, as well as co-cultured with unstimulated or stimulated (CL097) PBMCs (D) or pDCs (E) from male and female donors in transwell system. Total of 16 independent donors in (D) or 12 independent donors in (E) , consisting of equal numbers of male and female donors. Absolute expression levels relative to untreated condition. Paired sets of a male- and female-donors were matched for each experiment including controls. Wilcoxon test paired (solid line); 2way ANOVA test (dotted line); *p<0.05**; p<0.005; ***p<0.0005; ****p<0.00005.
Article Snippet: NK cells were isolated from PBMCs using
Techniques: Activation Assay, Enzyme-linked Immunosorbent Assay, Derivative Assay, Whisker Assay, MANN-WHITNEY, Co-Culture Assay, Control, Cell Culture, Expressing
Journal: Frontiers in Immunology
Article Title: Sex-dependent differences in type I IFN-induced natural killer cell activation
doi: 10.3389/fimmu.2023.1277967
Figure Lengend Snippet: NK cell-intrinsic sex differences in response to TLR7/8 stimulation. (A, B) Relative activation of CD69+ NK cells, separated by sex, after overnight cultures with control stimulations, as well as co-cultures with unstimulated and CL097-stimulated PBMCs (A) or pDCs (B) in transwell system. Activation levels were relativized to their own control condition (untreated). (C, D) Relative activation levels measured by CD69+ NK cells by further separating the sex of NK cells- and PBMCs-derived donors (C) or pDCs-derived donors (D) . Activation levels were relativized to their own control condition (untreated). Total of 16 independent donors in (D) or 12 independent donors in (E) , consisting of equal number of male and female donors. Paired sets of a male- and female-donors were matched for each experiment, including controls. Male NK cells (yellow); female NK cells (turquoise). Wilcoxon test paired (solid line); 2way ANOVA test (dotted line); ns, non-significant; *p<0.05; **p<0.005; ***p<0.0005; ****p<0.00005.
Article Snippet: NK cells were isolated from PBMCs using
Techniques: Activation Assay, Control, Derivative Assay