3 research outputs found

    Tumor onset is accelerated in TRAMP mice lacking iNKT cells.

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    <p>Age- and sex-matched male TRAMP (white bars; n = 97), TRAMPJα18<sup>−/−</sup> (black bars; n = 51) and WT mice (gray bars; n = 97) were killed at the indicated week after birth and the anatomy and histology of the UGA was analyzed as indicated in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0008646#s2" target="_blank">Material and Methods</a> section. Animals affected by neuroendocrine tumors were excluded. A, UGA weight (g), expressed as average±SEM, of TRAMP, TRAMPJα18<sup>−/−</sup> and WT mice killed at weeks 6–8 (n = 5, 8 and 19, respectively), 12–16 (n = 16, 17 and 26), 17–24 (n = 30, 15 and 26) and 25–28 (n = 46, 11 and 26), respectively. B, ratio of the weight of UGA and body weight subtracted of the UGA in the groups of animals reported above. C, Disease score, expressed as average±SEM, of the groups of animals reported above. Statistical analysis of collected data was performed using the Student's <i>t</i>-test (A and B) and the Mann-Whitney test (C); ***p<0.001, **0.001</p

    Survival of TRAMP mice lacking iNKT cells is reduced.

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    <p>Kaplan-Maier plot reporting the survival curves of groups of male TRAMP (black squares; n = 21) and TRAMPJα18<sup>−/−</sup> mice (black circles; n = 21). Animals were examined twice a week and euthanized when signs of bulky prostate tumor and/or distress were manifest. At necropsy, the anatomy and histology of the UGA was analyzed as indicated in the <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0008646#s2" target="_blank">Material and Methods</a> section. Animals were attributed a disease score≥4. Statistical comparison (Log-Rank test) between the survival curves: p<0.0001.</p

    αGal-Cer-mediated release of iNKT-associated cytokines.

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    <p>αGalCer (2 µg/mouse) was administered i.v. to TRAMP (white circles) and WT (black circles) littermates, and blood samples were collected from the tail vein 2, 6 and 24 hours later, and the serum content of IL-4 and IFN-γ was determined by standard ELISA. Values are reported as concentration of the cytokine (pg/ml) in the sera of each animal (3–4/experimental group) analyzed at the indicated time points. Reported data are representative of at least two independent experiments.</p
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