7 research outputs found
Premature Expression of Foxp3 in Double-Negative Thymocytes
<div><p>Peripheral immune regulation depends on the generation of thymic-derived regulatory T (tT<sub>reg</sub>) cells to maintain self-tolerance and to counterbalance overshooting immune responses. The expression of the T<sub>reg</sub> lineage defining transcription factor Foxp3 in developing tT<sub>reg</sub> cells depends on TCR signaling during the thymic selection process of these T cells. In this study, we surprisingly identify Foxp3<sup>+</sup> immature thymocytes at the double-negative (DN) stage in transcription factor 7 (Tcf7)-deficient mice. These Foxp3<sup>+</sup> cells did not express a TCR (β or γδ chains), CD3 or CD5 and therefore these cells were true DN cells. Further investigation of this phenomenon in a transgenic TCR model showed that Foxp3-expressing DN cells could not respond to TCR stimulation <i>in vivo</i>. These data suggest that Foxp3 expression in these DN cells occurred independently of TCR signaling. Interestingly, these Foxp3<sup>+</sup> DN cells were located in a transition state between DN1 and DN2 (CD4<sup>-</sup>CD8<sup>-</sup>CD3<sup>-</sup>TCR<sup>-</sup>CD44<sup>high</sup>CD25<sup>low</sup>). Our results indicate that Tcf7 is involved in preventing the premature expression of Foxp3 in DN thymocytes.</p></div
Foxp3 expression at the DN cell stage in Tcf7-deficient mice.
<p>(A) Representative plots and quantification of Foxp3 staining in CD4<sup>-</sup>CD8<sup>-</sup> (DN) thymocytes from Tcf7<sup>+/+</sup> and Tcf7<sup>-/-</sup> mice (n = 8). (B) Left panels: Representative plots showing Foxp3 and intracellular (IC) TCRβ staining in DN thymocytes from Tcf7<sup>+/+</sup> and Tcf7<sup>-/-</sup> mice. Middle panels: TCRγδ and CD3 staining on DN Foxp3<sup>+</sup>TCRβ<sup>-</sup> cells (gate R1). Right panel: Quantification of DN Foxp3<sup>+</sup>TCRβ<sup>-</sup>TCRγδ<sup>-</sup>CD3<sup>-</sup> cells (gate R2) depicted as the percentage of total DN cells (n = 6). (C) Left panel: Representative histograms showing CD5 staining on Foxp3<sup>+</sup> DN, Foxp3<sup>+</sup> DP, and Foxp3<sup>+</sup> CD4SP cells from Tcf7<sup>-/-</sup> mice. Right panel: Quantification of CD5 geometric mean from DN, DP, and CD4SP Foxp3<sup>+</sup> or Foxp3<sup>-</sup> populations (n = 3). Mean + SD are shown for all quantified data. Numbers show percentages of cells within the indicated box. Each symbol represents an individual animal. ** P < 0.01 (unpaired t-test).</p
Analysis of Foxp3<sup>+</sup> DN cells in TEa-Tcf7-deficient mice.
<p>(A) Representative plots showing TCRVβ6 and TCRVα2 expression on CD4SP thymocytes from TEa-Tcf7<sup>+/+</sup> and TEa-Tcf7<sup>-/-</sup> mice in the presence or absence of cognate antigen (Ag). The Tg TCR population is divided into TCR<sup>high</sup> and TCR<sup>low</sup> populations. (B-C) Quantification of the percentage of total (B) or TCR<sup>high</sup> (C) TCRVβ6<sup>+</sup>TCRVα2<sup>+</sup> cells among CD4SP thymocytes (n = 8). (D) Representative plots showing Foxp3 expression in DN TCRVβ6<sup>+</sup>TCRVα2<sup>+</sup> thymocytes from TEa-Tcf7<sup>+/+</sup> and TEa-Tcf7<sup>-/-</sup> mice in the absence of Ag. (E) Quantification of Foxp3<sup>+</sup> DN TCRVβ6<sup>+</sup>TCRVα2<sup>+</sup> thymocytes from TEa-Tcf7<sup>+/+</sup> and TEa-Tcf7<sup>-/-</sup> mice in the presence or absence of Ag (n = 8). (F-G) Representative plots showing TCRVβ6 and TCRVα2 expression on DN Foxp3<sup>+</sup> (F) or CD4SP Foxp3<sup>+</sup> (G) thymocytes from TEa-Tcf7<sup>+/+</sup> and TEa-Tcf7<sup>-/-</sup> mice in the presence or absence of Ag. Cells are pre-gated on TCRVβ6<sup>+</sup>TCRVα2<sup>+</sup>. Each dot represents one individual animal and mean is shown for all quantified data. Numbers show percentages of cells within the indicated box. NS, not significant, *** P < 0.001, **** P < 0.0001 (unpaired t-test).</p
Genotypical comparison of T<sub>reg</sub> and T<sub>conv</sub> cells isolated from brown adipose tissue (BAT) and spleen tissue (SPL) in cold- and warm-conditioned animals generated with an Illumina Mouse Expression Array.
<p>(A) Gene expression profiles comparing T<sub>reg</sub> (top) or T<sub>conv</sub> (bottom) cell populations between spleen and adipose tissue samples isolated from warm-conditioned animals (left) or between cells isolated from cold vs warm-conditioned animals (right). Numbers indicate genes either up- or downregulated more than 2-fold (cut-off: dotted line), with the number of significantly different (p<0.05) genes shown in brackets with an asterisk. (B) Volcano plot comparing gene expression and significance values between T<sub>reg</sub> and T<sub>conv</sub> genes isolated from BAT in warm-conditioned animals. Key up- or downregulated genes in T<sub>reg</sub> cells are annotated (Foxp3, Il10, Cxcl1/2, Tcf7, Ifng) and serve as quality control to the published consensus T<sub>reg</sub>-cell signature. (C) Hierarchical clustering of the top-30 upregulated genes and the top-10 downregulated genes in warm-conditioned brown adipose tissue T<sub>reg</sub> cells versus spleen T<sub>reg</sub> cells. (D) Comparison of BAT-T<sub>reg</sub>-specific genes with visceral adipose tissue (VAT)-specific genes. We first determined 430 genes to upregulated in BAT warm-conditioned T<sub>reg</sub> cells, with 222 genes being significantly altered (p<0.05). We then overlaid BAT T<sub>reg</sub>-upregulated genes with VAT T<sub>reg</sub> tissue specific expression gene data. 181 genes were matched between both microarary chips, with 169 genes also upregulated in VAT, and only 12 genes specific for BAT (left). The corresponding analysis of the 516 genes upregulated in cold BAT T<sub>reg</sub> cells versus warm spleen T<sub>reg</sub> cells revealed 194 genes to be significantly upregulated. 158 could be matched to VAT T<sub>reg</sub>-specific genes, of which 148 were VAT-specific, whereas only 10 were specific for BAT. P-values indicate the significance of overrepresentation of BAT T<sub>reg</sub>-specific genes in the VAT T<sub>reg</sub> signature. (E) Comparison of VAT-T<sub>reg</sub> specific genes on BAT warm (left) or BAT cold (right) gene signatures. Of 1839 genes specifically overexpressed in VAT T<sub>reg</sub> cells, 1059 were statistically significantly (p<0.05) upregulated. Of these 1059 genes, 829 were also detectable in the BAT T<sub>reg</sub> microarray. When comparing the VAT T<sub>reg</sub> signature to warm BAT T<sub>reg</sub> cells, 660 genes were overrepresented in VAT, whereas cold BAT T<sub>reg</sub> cells show 685 genes to be overrepresented in VAT.</p
Inflammatory status of adipose tissue.
<p>Real-time RT-PCR analysis of (A) brown adipose tissue (BAT) and (B) subcutaneous white adipose tissue of T<sub>reg</sub> cell-proficient (PBS) and T<sub>reg</sub> cell-deficient (DT) mice after cold exposure. Ucp1, uncoupling protein 1; Cidea,cell death-inducing DNA fragmentation factor, alpha subunit-like effector A; Dio2,deiodinase, iodothyronine, type II; Pparg, peroxisome proliferator-activated receptor gamma; Prdm16, PR domain containing 16; Cd68, Cd68 antigen; Ccl2,chemokine (C-C motif) ligand 2; Tnfa, tumor necrosis factor alpha; Ifng, interferon, gamma; Mrc1, mannose receptor, C type 1; Mgl1, macrophage galactose-type C-type lectin 1; Arg1,arginase 1; Il-10, interleukin 10; Il-4, interleukin 4. Data are mean ± SD (n = 9–10); *p<0.05 (Student’s t-test). (C) Representative hematoxylin and eosin (H&E) staining (left) and immunohistochemical anti-MAC-2 staining (right; brown color) in BAT from PBS and DT mice. Scale bar 100 μm. Quantification of MAC-2 positive area (panel below MAC-2 staining) as a percentage of total area.</p
Principal biological processes affected by T<sub>reg</sub> cell depletion in BAT.
<p>Principal biological processes affected by T<sub>reg</sub> cell depletion in BAT.</p
Physiological parameters.
<p>(A) Body weight (BW) and (B) adipose tissues weights of T<sub>reg</sub> cell-proficient (PBS) and T<sub>reg</sub> cell-deficient (DT) mice after cold exposure. BAT, brown adipose tissue; scWAT, subcutaneous white adipose tissue, aWAT, abdominal white adipose tissue. (C) Blood glucose, (D) serum non-estherified fatty acids (NEFA) and (E) serum triglycerides in PBS and DT mice. Values are mean ± SD (n = 9–10); *P<0.05 (Student’s t-test).</p