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. 2018 Feb 28;9:371. doi: 10.3389/fimmu.2018.00371

Figure 4.

Figure 4

Abnormal germinal center (GC) structure and somatic hypermutation (SHM) in Ptenfl/fl Cγ1Cre/+ mice. (A) Representative flow cytometry analysis of GC light zone (LZ) and dark zone (DZ) splenocytes from Pten+/+ Cγ1Cre/+ and Ptenfl/fl Cγ1Cre/+ mice at day 7 after SRBC immunization. Data were given from one representative of at least two independent experiments (n = 4 for each group). The cells were pregated in GCBs. (B) The statistical quantification of the flow cytometry data of LZ (left) and DZ (right) splenocytes as shown in (A). Each symbol represents an individual animal (four mice for each group). The data represent the mean ± SD. Two-tailed t-tests were performed for statistical comparisons. (C) Representative flow cytometry analysis of GC LZ and DZ from Pten+/+ Cγ1Cre/+ and Ptenfl/fl Cγ1Cre/+ mice at day 14 after VLP injection (left). Statistical comparison for LZ (middle) and DZ (right) cells percentage of total GCBs was also shown. The data represent the mean ± SD of six mice per group in three independent experiments. Two-tailed t tests were performed for statistical comparisons. (D) The affinity maturation of the NP-specific IgM, IgG1, IgG2b, and IgG3 antibodies in Pten+/+ Cγ1Cre/+ versus Ptenfl/fl Cγ1Cre/+ mice as determined by the ratio NP8/NP30. The data represent the median ± interquartile range from three independent experiments with six mice per group at the indicated time point and were analyzed with Kruskal–Wallis test. *p < 0.05; **p < 0.01.