SlideServe
Menu
Préférences
© SlideServe · v2026

Impact of Dll3 Deficiency on T Cell Development and Function in Thymus

astra-potter avatar
4 diapositives · 171 Views · Nov 17, 2014

This supplementary file presents three figures related to the effects of Dll3 deficiency on T cell development and function. The first figure illustrates the normal development of wild-type T cells in a Dll3-/- host using irradiation chimeras. Figure two shows that negative selection of autoreactive CD4+ T cells is unaffected by Dll3 deficiency, featuring representative flow cytometry plots and histograms. The third figure demonstrates the dependence of T cell production from Dll3-/- precursors on Notch cleavage by g-secretase, indicating critical mechanisms of T cell lineage differentiation.

Impact of Dll3 Deficiency on T Cell Development and Function in Thymus - slide 1
01 / 4Impact of Dll3 Deficiency on T Cell Development and Function in Thymus
1 / 17

Télécharger la présentation

Impact of Dll3 Deficiency on T Cell Development and Function in Thymus
Une image / un lien ci-dessous est fourni (tel quel) pour télécharger la présentation

Politique de téléchargement : le contenu du site vous est fourni TEL QUEL pour votre information et votre usage personnel ; il ne peut être vendu, concédé sous licence ni partagé sur d’autres sites sans l’accord de son auteur.Le contenu vous est fourni TEL QUEL, pour votre information et votre usage personnel uniquement. Téléchargez la présentation en cliquant sur ce lien. Lors du téléchargement, si vous ne parvenez pas à télécharger une présentation, l’éditeur a peut-être supprimé le fichier de son serveur.Pendant le téléchargement, si vous ne parvenez pas à obtenir une présentation, le fichier a peut-être été supprimé par l’éditeur.

F I N

Plus de contenu associé

Transcription de la présentation
  1. The Supplementary file contains three figures with figure legends. The files submitted as a 1997-2003 Powerpoint file.

  2. a NS 108 107 # DP cells 106 105 Wt >Wt Wt>Dll3-/- b 108 NS 107 #CD4+ cells 106 105 Wt >Wt Wt>Dll3-/- c 108 NS 107 #CD8+ cells 106 105 Wt >Wt Wt>Dll3-/- Supplemental Figure 1. Wild type T cells develop normally in a Dll3-/- host. Irradiation chimeras were set up using bone marrow cells from wild type CD45.1+ donor animals and these were transferred to irradiated Dll3+/+(CD45.2) or Dll3-/- (CD45.2) recipient mice. Twelve weeks after the transfer the thymus and spleen were removed and cells analysed by flow cytometry. The data shows the number of CD45.1+ (a) DP cells, (b) CD4+ and (c) CD8+ T cells in the thymus. Unpaired t test was used to test for statistically significant differences between groups. NS = not significant. Supplemental Figure 1 Hoyne et al

  3. Supplemental Figure 2 Hoyne et al Dll3-/- : CD45.1 > insHel Dll3+/+: CD45.1 > insHel a CD4 CD8 Gated on CD4+ cells CD4 1G12 b 35 65 55 45 Gated on DP cells 45 55 30 70 c CD45.1 CD45.1 cells 100 100 CD45.2 cells 10 10 #CD4 1G12+ (x 106 ) #CD4 1G12+ (x 106 ) 1 1 0.1 0.1 0.01 0.01 1 10 100 1 10 100 #DP cells (x106) #DP cells (x106) Supplemental Figure 2. Negative selection of autoreactive CD4+ T cells is not affected by Dll3 deficiency. a. Representative FACS dot plots showing CD4 v CD8 expression of total thymocytes from a Dll3+/+ TCR:TCR+CD45.1+ > insHel mice or Dll3-/- TCR+:TCR+CD45.1+ > insHel mice (top panel). Lower panel shows CD4 v 1G12 staining on the CD4 gated thymocyte population. b. Representative histograms showing the proportion of CD45.1+ and CD45.1-ve cells in the DP or CD4+ 1G12+ gates of representative chimaeras. c. Total cell numbers of DP and CD4+ 1G12+ cells in the thymus of individual chimaeric mice. Cells from the Dll3+/+:CD45.1 chimeras (filled squares), and Dll3-/-:CD45.1 chimaeras (open triangles) are shown.

  4. Dll3+/+ 100 100 80 80 60 60 40 40 % T cells % B cells 20 20 0 0 0 0.1 0.3 1 L-685,458concentration (mM) Dll3-/- 100 100 80 80 60 60 % B cells 40 40 % T cells 20 20 0 0 0 0.1 0.3 1 L-685,458concentration (mM) Supplemental Figure 3. T cell production by Dll3-/- precursors is dependent on Notch cleavage by g-secretase. Lineage negative DN cells isolated from the thymus of either Dll3+/+ or Dll3-/- mice were cultured on OP9-Dll1 cells in the presence or absence of the g-secretase inhibitor L-685,458 (Calbiochem, gsi-X) at the indicated concentrations. FACS analysis of Thy1 versus B220 expression was made 8 days after commencement of the culture. The graphs show the frequency of B cells (B220+) (black squares) and T cells (Thy1+) (white squares) arising in the same cultures. Top graph shows the T vs B cell production in Dll3+/+ derived cells and lower graph shows T vs B cells derived from Dll3-/- progenitors. Each point represents the average of 6 replicate wells and is representative of one of three assays performed. Supplemental Figure 3 Hoyne et al