Figure 1
Figure 1. Visualizing the segregation of CD4 and CD8 TM reservoirs in mice. (A) Schematic representation of dual-reporter retrovector MFG. LTR indicates long-term repeats; Fluc, firefly luciferase; P2A, porcine teschovirus 2A sequence; EGFP, enhanced green fluorescence protein; and WRE, woodchuck responsive element. (B,C) Visualization of the CD4 and CD8 TM formation in albino B6 mice postadoptive transfer of 1 × 106 MFG-labeled OT2 (CD4) or OT1 (CD8) effector T cells (TEs) using BLI. Representative BLI images (B) and the measurements of total body luminescence (TBL, mean ± SEM; C) are shown (n = 4). Shaded area marks contraction phase (C). (D,E) Visualization of the CD4 and CD8 TMs in individual tissues using excised tissue BLI. (D) Tissues were collected from albino B6 recipient mice 2 months after transfer of 10 × 106 MFG-labeled OT2 (CD4) or OT1 (CD8) TEs. PLN indicates peripheral lymph node; MLN, mesenteric LN; SP, spleen; BM, bone marrow; Thy, thymus; GT, genital tract; and Savi, salivary gland. (E) Detailed analysis of CD4 TM homing to gut. BLI images of the gut tract (top, the “hot spots” are numbered), identification of the “hot spots” as Peyer patches (PPs; middle), and the measurements of luminescence in gut sub-regions (bottom) are shown. Data are representative of 3 independent experiments. (F) Visualization of the antigen-specific or polyclonal CD4 and CD8 TMs formed in albino B6 recipient mice each receiving 1 × 106 either MFG-labeled OT2 or OT1 TEs, or MFG-labeled B6 CD4 or CD8 TEs using BLI. Representative BLI images collected 1 month after transfer are shown (n = 4). Schematic showing the individual tissue localization in mice is provided for reference. CLNs indicate cervical LNs; A/BLNs, axillary/brachial LNs; and IgLN, inguinal LNs. PLNs refer to the combination of CLNs, A/BLNs, and IgLNs.

Visualizing the segregation of CD4 and CD8 TM reservoirs in mice. (A) Schematic representation of dual-reporter retrovector MFG. LTR indicates long-term repeats; Fluc, firefly luciferase; P2A, porcine teschovirus 2A sequence; EGFP, enhanced green fluorescence protein; and WRE, woodchuck responsive element. (B,C) Visualization of the CD4 and CD8 TM formation in albino B6 mice postadoptive transfer of 1 × 106 MFG-labeled OT2 (CD4) or OT1 (CD8) effector T cells (TEs) using BLI. Representative BLI images (B) and the measurements of total body luminescence (TBL, mean ± SEM; C) are shown (n = 4). Shaded area marks contraction phase (C). (D,E) Visualization of the CD4 and CD8 TMs in individual tissues using excised tissue BLI. (D) Tissues were collected from albino B6 recipient mice 2 months after transfer of 10 × 106 MFG-labeled OT2 (CD4) or OT1 (CD8) TEs. PLN indicates peripheral lymph node; MLN, mesenteric LN; SP, spleen; BM, bone marrow; Thy, thymus; GT, genital tract; and Savi, salivary gland. (E) Detailed analysis of CD4 TM homing to gut. BLI images of the gut tract (top, the “hot spots” are numbered), identification of the “hot spots” as Peyer patches (PPs; middle), and the measurements of luminescence in gut sub-regions (bottom) are shown. Data are representative of 3 independent experiments. (F) Visualization of the antigen-specific or polyclonal CD4 and CD8 TMs formed in albino B6 recipient mice each receiving 1 × 106 either MFG-labeled OT2 or OT1 TEs, or MFG-labeled B6 CD4 or CD8 TEs using BLI. Representative BLI images collected 1 month after transfer are shown (n = 4). Schematic showing the individual tissue localization in mice is provided for reference. CLNs indicate cervical LNs; A/BLNs, axillary/brachial LNs; and IgLN, inguinal LNs. PLNs refer to the combination of CLNs, A/BLNs, and IgLNs.

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