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Image Search Results
Journal: PLoS Pathogens
Article Title: Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
doi: 10.1371/journal.ppat.1007611
Figure Lengend Snippet: Ileum and colon tissues were collected from mouse recipients at 21 days post gavage and analyzed for frequencies of CD69+ and CD103+ T cells. (A) Gating strategy for CD69+ T cells. Representative plots from ileum tissues are shown. (B-C) Frequencies of (B) CD69+ CD8+ T cells, (C) CD103+ CD8+ T cells, and (D) CD103+ CD4+ T cells in the ileum. (E) Frequencies of CD69+ CD4+ T cells in the colon. Each data point represents a single mouse gavaged with an individual donor’s feces, and a representative mouse was used for stools tested in replicate mice. Lines represent medians. Statistical analyses were performed using t-tests to compare groups if data from both groups had normal distributions and Mann-Whitney tests to compare groups if data from at least one group had a non-parametric distribution. ** = p<0.01, * = p<0.05.
Article Snippet: 0.5–1 x 10 6 ileum and colon cells from each mouse were stained in FACS buffer for 30 min at 4° C with the following antibodies: CD3-PerCP-Cy5.5 (17A2, Biolegend), CD4-FITC (RM4-4, eBioscience), CD8-BV510 (53–6.7, Biolegend),
Techniques: MANN-WHITNEY
Journal: PLoS Pathogens
Article Title: Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
doi: 10.1371/journal.ppat.1007611
Figure Lengend Snippet: mLN from mouse recipients were collected and analyzed for effector memory CD4+ T cell frequency (CD44+ CD62L-) using flow cytometry. (A) Comparison of frequencies of CD44+ CD62- CD4+ T cells in the mLN across recipient groups. (B) Spearman correlations of effector memory CD4+ T cell (T em ) frequencies in the mLN with frequencies of CD69+ CD4+ T cells in the colon. Each data point represents a single mouse gavaged with an individual donor’s feces, and a representative mouse was used for stools tested in replicate mice. Lines represent medians. Statistical analyses were performed using t-tests to compare groups if data from both groups had normal distributions and Mann-Whitney tests to compare groups if data from at least one group had a non-parametric distribution. * = p<0.05.
Article Snippet: 0.5–1 x 10 6 ileum and colon cells from each mouse were stained in FACS buffer for 30 min at 4° C with the following antibodies: CD3-PerCP-Cy5.5 (17A2, Biolegend), CD4-FITC (RM4-4, eBioscience), CD8-BV510 (53–6.7, Biolegend),
Techniques: Flow Cytometry, MANN-WHITNEY
Journal: PLoS Pathogens
Article Title: Gut microbiota from high-risk men who have sex with men drive immune activation in gnotobiotic mice and in vitro HIV infection
doi: 10.1371/journal.ppat.1007611
Figure Lengend Snippet: Microbial correlates with donor/recipient T cell activation and gut homing, and in vitro HIV infection.
Article Snippet: 0.5–1 x 10 6 ileum and colon cells from each mouse were stained in FACS buffer for 30 min at 4° C with the following antibodies: CD3-PerCP-Cy5.5 (17A2, Biolegend), CD4-FITC (RM4-4, eBioscience), CD8-BV510 (53–6.7, Biolegend),
Techniques: Activation Assay, In Vitro, Infection
Journal: The Journal of Cell Biology
Article Title: The N terminus of SKAP55 enables T cell adhesion to TCR and integrin ligands via distinct mechanisms
doi: 10.1083/jcb.201305088
Figure Lengend Snippet: SKAP55 is required for microcluster persistence and movement, and for contact stability. (A) Confirmation of the efficacy of SKAP55 knockdown and add-back in stable SKAP55 knockdown cells (JSKAP.SY) with or without transient reconstitution ( n = 3). (B) J14.SY and JSKAP.SY cells expressing mRFP1 or SKAP55.mRFP1 were stimulated on coverslips and imaged for at least 5 min. Representative MOT images and kymographs are shown. Bars: (MOT images) 10 µm; (kymographs) 5 µm × 60 s. See for microcluster properties and experiment numbers. (C) Composite microcluster traces for the conditions examined in B. Numbers in parentheses indicate the total number of cells examined. Line intensity corresponds to the fraction of microclusters surviving; arrowheads identify points of half-maximal microcluster dissociation. (D) Fraction of the contact area engaged in fluctuation (see Fig. S1 , F and G; n = 3). (E) Fraction of cells scored as displaying unstable contacts (see Fig. S1, I and J; n = 5). (F) Surface expression of CD69 in J14.SY and JSKAP.SY cells, after normalization to a TCR-stimulated J14.SY control ( n = 4). (G) Kinetics of Erk1/2 phosphorylation in J14.SY and JSKAP.SY stimulated for the indicated time points ( n = 3). Error bars indicate mean ± SEM. From parental J14.SY cells (with or without mRFP1): **, P < 0.01. From JSKAP.SY (with or without mRFP1): ##, P < 0.01.
Article Snippet: Western blotting was conducted with antibodies directed against ADAP (BD), β1 integrin (EP1041Y; Abcam),
Techniques: Knockdown, Expressing, Control, Phospho-proteomics
Journal: Biology of Reproduction
Article Title: Immune response to a model shared placenta/tumor-associated antigen reduces
cancer risk in parous mice
doi: 10.1095/biolreprod.116.144907
Figure Lengend Snippet: Antibodies used for flow cytometry.
Article Snippet: Cells were detected by flow cytometry using Streptavidin-APC (Jackson ImmunoResearch Laboratories, Inc., West Grove, PA). table ft1 table-wrap mode="anchored" t5 Table 1. caption a7 Fluorophore Vendor; catalog number CD8 Pacific blue Biolegend; 100725 CD19 APC Biolegend; 115512 CD44 APC-Cy7 Biolegend; 103028 ICOS PE-Cy5 Biolegend;
Techniques: Cytometry