<p>Splenocytes were isolated from WT and OGR1-KO mice and T cells were depleted by MACs separation as described in the Methods. T cell-depleted splenocytes (APC) were stimulated with LPS overnight, washed and co-cultured (1:1 ratio) with CFSE-labeled WT CD4<sup>+</sup> T cells that were plated onto anti-CD3 antibody-coated plates. The percentage of divided CD4<sup>+</sup> cells (A-B) was examined after 3 days of culture. Data shown are from 4 individual experiments. (C-D) Cells were stimulated with PMA, ionomycin in the presence of brefeldin A for an additional 4 hours and intracellular staining for IFN-γ was performed. (C) shows representative FACs plots of IFN-γ expression versus side scatter of CD4<sup>+</sup> cells and (D) shows the mea...
(A) Representative flow cytometry analysis of CD4+ Foxp3+ cells among CD3+ cells from spleen, lung, ...
<p>Splenocytes from WT or <i>Itk</i>-KD mice were activated <i>in vitro</i> with PMA (50 ng/ml)/iono...
<p>Wild type and PGRN-deficient mice were injected intraperitoneally with BrdU labeling reagents, an...
<p>(A) Splenocytes were isolated from six to eight-week-old mice and stained with 5 µM CFSE and stim...
<p>(A-B) Mice (N = 6/group) were immunized with MOG<sub>35-55</sub>/CFA and at 10 days post-immuniza...
<p>Ly6G-enriched PECs and splenocytes from MOSEC-bearing WT and p47<i><sup>phox−/−</sup></i> mice (d...
<p>T cells from p18<sup>ink4c</sup>+/+ (dark gray symbols) or p18<sup>ink4c</sup>−/− (light gray sym...
<p>To analyze IFN-γ- or IL-10-producing CD4<sup>+</sup> T cells, unfractionated spleen cells of P- o...
<p>Splenocytes were stained for CD4, Foxp3, CD44 and CD62L. CD4<sup>+</sup>Foxp3<sup>−</sup> T cells...
<p>Ag-specific T cell proliferative responses were evaluated by [<sup>3</sup>H] thymidine incorporat...
<p>(A) Number of CD4<sup>+</sup> T-cells (mean±1 SD) that infiltrated into (left, <i>n</i> = 3) and ...
<p>CD4<sup>+</sup>CD25<sup>+</sup> T cells from 12–15 week-old B6 or Sick NOD mice were cultured ove...
<p>Spleens were harvested at D5 and splenocytes were rapidly isolated in order to determine T cells ...
<p>(<b>A–C</b>) Total thymocytes were left unstimulated or stimulated with PMA (50 ng/ml) and ionomy...
<p>One week after the third immunization, spleens were collected from mice. Splenocytes were suspend...
(A) Representative flow cytometry analysis of CD4+ Foxp3+ cells among CD3+ cells from spleen, lung, ...
<p>Splenocytes from WT or <i>Itk</i>-KD mice were activated <i>in vitro</i> with PMA (50 ng/ml)/iono...
<p>Wild type and PGRN-deficient mice were injected intraperitoneally with BrdU labeling reagents, an...
<p>(A) Splenocytes were isolated from six to eight-week-old mice and stained with 5 µM CFSE and stim...
<p>(A-B) Mice (N = 6/group) were immunized with MOG<sub>35-55</sub>/CFA and at 10 days post-immuniza...
<p>Ly6G-enriched PECs and splenocytes from MOSEC-bearing WT and p47<i><sup>phox−/−</sup></i> mice (d...
<p>T cells from p18<sup>ink4c</sup>+/+ (dark gray symbols) or p18<sup>ink4c</sup>−/− (light gray sym...
<p>To analyze IFN-γ- or IL-10-producing CD4<sup>+</sup> T cells, unfractionated spleen cells of P- o...
<p>Splenocytes were stained for CD4, Foxp3, CD44 and CD62L. CD4<sup>+</sup>Foxp3<sup>−</sup> T cells...
<p>Ag-specific T cell proliferative responses were evaluated by [<sup>3</sup>H] thymidine incorporat...
<p>(A) Number of CD4<sup>+</sup> T-cells (mean±1 SD) that infiltrated into (left, <i>n</i> = 3) and ...
<p>CD4<sup>+</sup>CD25<sup>+</sup> T cells from 12–15 week-old B6 or Sick NOD mice were cultured ove...
<p>Spleens were harvested at D5 and splenocytes were rapidly isolated in order to determine T cells ...
<p>(<b>A–C</b>) Total thymocytes were left unstimulated or stimulated with PMA (50 ng/ml) and ionomy...
<p>One week after the third immunization, spleens were collected from mice. Splenocytes were suspend...
(A) Representative flow cytometry analysis of CD4+ Foxp3+ cells among CD3+ cells from spleen, lung, ...
<p>Splenocytes from WT or <i>Itk</i>-KD mice were activated <i>in vitro</i> with PMA (50 ng/ml)/iono...
<p>Wild type and PGRN-deficient mice were injected intraperitoneally with BrdU labeling reagents, an...