Figure 4
Glce−/− mice have reduced basal serum Ig levels, an attenuated antigen-dependent immune response, and reduced plasma cell numbers. (A) Serum Ig concentrations in nonimmunized Glce+/+ and Glce−/− mice. The concentration of Igs of different isotypes was measured by ELISA, preceding immunization with TNP-KLH. Bars represent the mean ± SD; n = 12. (B) The timeline of the immunization protocol. Glce+/+ and Glce−/− mice were immunized at 3 (primary, boost, reboost) subsequent time points (▿). Blood samples were taken and serum was isolated (▲). Mice were killed at 84 and 150 days () after primary immunization for analysis of the BM plasma cells. (C) TNP-specific antibody levels after immunization with TNP-KLH. ELISA was performed to measure the TNP-specific antibody titer of the IgM, IgG1, and IgG2b isotypes. ■ represents Glce+/+ mice; and □, Glce−/− mice. Outliers and nonresponders were statistically excluded. These graphs represent 3 independent experiments of at least 4 to 8 mice (mean ± SEM). (D) Number of BM plasma cells (day 84). Tissue sections of femurs obtained at autopsy were stained for κ-light chain to quantify the number of plasma cells per optic field (original magnification, × 40) (mean ± SEM; n = 4/group). (E) Number of BM plasma cells (day 150). Whole BM was isolated and BM plasma cells (B220−, syndecan-1+, Ly6c+) were quantified by FACS as percentage of total BM cells (mean ± SD, n = 4/group). (F) Total serum Ig concentrations in Glce+/+ and Glce−/− mice (day 49). The concentration of Igs of different isotypes was measured by ELISA after repeated immunization with TNP-KLH. Bars represent the mean ± SD; n = 12. *P < .05.

Glce−/− mice have reduced basal serum Ig levels, an attenuated antigen-dependent immune response, and reduced plasma cell numbers. (A) Serum Ig concentrations in nonimmunized Glce+/+ and Glce−/− mice. The concentration of Igs of different isotypes was measured by ELISA, preceding immunization with TNP-KLH. Bars represent the mean ± SD; n = 12. (B) The timeline of the immunization protocol. Glce+/+ and Glce−/− mice were immunized at 3 (primary, boost, reboost) subsequent time points (▿). Blood samples were taken and serum was isolated (▲). Mice were killed at 84 and 150 days () after primary immunization for analysis of the BM plasma cells. (C) TNP-specific antibody levels after immunization with TNP-KLH. ELISA was performed to measure the TNP-specific antibody titer of the IgM, IgG1, and IgG2b isotypes. ■ represents Glce+/+ mice; and □, Glce−/− mice. Outliers and nonresponders were statistically excluded. These graphs represent 3 independent experiments of at least 4 to 8 mice (mean ± SEM). (D) Number of BM plasma cells (day 84). Tissue sections of femurs obtained at autopsy were stained for κ-light chain to quantify the number of plasma cells per optic field (original magnification, × 40) (mean ± SEM; n = 4/group). (E) Number of BM plasma cells (day 150). Whole BM was isolated and BM plasma cells (B220, syndecan-1+, Ly6c+) were quantified by FACS as percentage of total BM cells (mean ± SD, n = 4/group). (F) Total serum Ig concentrations in Glce+/+ and Glce−/− mice (day 49). The concentration of Igs of different isotypes was measured by ELISA after repeated immunization with TNP-KLH. Bars represent the mean ± SD; n = 12. *P < .05.

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