Figure 6.
Figure 6. Prevention of diabetes and insulitis in NOD mice after intrathymic injection of a preproinsulin-2–expressing lentiviral vector. (A) Cumulative diabetes incidence (Kaplan-Meier survival curve) in unmanipulated mice (CTRL, n = 11) or after intrathymic injection of a GFP-expressing (LvGFP, n = 10) or preproinsulin-2–expressing (LvPpins2, n = 14) lentiviral vector. Indicated for LvGFP and LvPpins2 survival curves are the P values calculated with a log-rank test relative to the untreated NOD mice. (B) Sections of formalin-fixed pancreas from 10-week-old untreated nondiabetic mice (top left: original magnification, ×20), 36-week-old LvGFP-treated diabetic mice (top right: original magnification, ×100), and LvPpins-2–treated nondiabetic mice (bottom left and right: original magnification, ×20). Paraffinembedded sections of pancreas from NOD mice were stained with hematoxylin for 5 minutes followed by eosin for 30 seconds to reveal nucleated cells. Images were taken with either a 10×/0.3 PL or a 20×/0.5 FLUOTAR AB objective of a DM RB microscope (Leica Microsystems, Wetzlar, Germany). Image digitization was performed by a DXC930P CDD color video camera (Sony France, Clichy, France) with TRIBVN ICS software v. 1.2.0.9 (TRIBVN, Châtillon, France). Images were processed for contrast and luminosity using Adobe Photoshop CS.

Prevention of diabetes and insulitis in NOD mice after intrathymic injection of a preproinsulin-2–expressing lentiviral vector. (A) Cumulative diabetes incidence (Kaplan-Meier survival curve) in unmanipulated mice (CTRL, n = 11) or after intrathymic injection of a GFP-expressing (LvGFP, n = 10) or preproinsulin-2–expressing (LvPpins2, n = 14) lentiviral vector. Indicated for LvGFP and LvPpins2 survival curves are the P values calculated with a log-rank test relative to the untreated NOD mice. (B) Sections of formalin-fixed pancreas from 10-week-old untreated nondiabetic mice (top left: original magnification, ×20), 36-week-old LvGFP-treated diabetic mice (top right: original magnification, ×100), and LvPpins-2–treated nondiabetic mice (bottom left and right: original magnification, ×20). Paraffinembedded sections of pancreas from NOD mice were stained with hematoxylin for 5 minutes followed by eosin for 30 seconds to reveal nucleated cells. Images were taken with either a 10×/0.3 PL or a 20×/0.5 FLUOTAR AB objective of a DM RB microscope (Leica Microsystems, Wetzlar, Germany). Image digitization was performed by a DXC930P CDD color video camera (Sony France, Clichy, France) with TRIBVN ICS software v. 1.2.0.9 (TRIBVN, Châtillon, France). Images were processed for contrast and luminosity using Adobe Photoshop CS.

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