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. 2014 Aug 21;9(8):e105370. doi: 10.1371/journal.pone.0105370

Figure 1. Augmentation of IgA production by LG2055 in vitro and in vivo.

Figure 1

Whole PP cells were cultured with or without each of the four Lactobacillus strains (LG2055, L. gasseri JCM1131t (LG1131T), L. helveticus SBT2171 (LH2171), L. acidophilus SBT2062 (LA2062), 10 µg/ml) for 7 days (A). Whole PP cells were cultured with 0, 0.1, 1.0, and 10 µg/ml of LG2055 for 7 days (B). Whole PP cells were cultured with or without LG2055 (10 µg/ml) for 3, 5, and 7 days (C) The amounts of IgA in culture supernatants were determined by ELISA. Each experiment was done with tripricate cultures; data are shown as the mean ± SD. The values for cells cultured with lactic acid bacteria are compared with that of without the bacteria by one-way ANOVA, Dunnett's post test (A and B) and the t-test (C). Significant differences are indicated by * P<0.05, ** P<0.01, *** P<0.001. LG2055 was orally administrated to BALB/c mice for 5 weeks. Amounts of total IgA in intestinal tissue extracts (D) were determined by ELISA. The population of IgA+ B220+ cells in PP cells (E) and IgA+ B220- cells in LP cells (F) was analyzed by FACS. Representative data from two independent experiments are shown. Data are shown as the mean ± SD (number of mice n = 10). Significant difference from control group at *P<0.05, **P<0.01 was shown by the t-test (D, E, and F).