Figure 1
Figure 1. Truncated IgM is present in serum of old L−/− mice. (A) Level of μHC in serum of 2- to 14-month-old L−/− mice determined by ELISA at 1/100 dilution. (B) A comparative analysis of IgM serum titers in L−/− (▴), C-region deletion (CΔ26) as a negative control (♦) and normal (NM) mice (■). Means and standard deviation were calculated from the 10 L−/− mice in panel A and 7 NM mice. (C) Western analysis of serum antibodies from L−/−, of different age in months (m) as indicated. Sera from L−/−, μNR, and NM mice were purified by incubation with anti–mouse Ig coupled to Sepharose, separated on Ready-Gels under reducing conditions, and visualized with antibodies against mouse IgM. (D) Flow cytometric analysis of spleen cells surface-stained for IgM and B220. A representative presentation of a 1-year-old L−/− mouse compared with NM and μNRL−/− animals. The upper histograms show that, in addition to B220+ IgM+ cells, an IgMbright B220− population can be found in old L−/− mice. This population is more abundant in μNRL−/− mice. Plotting forward scatter (FSC) against IgM shows an IgMbright population of small particles with percentages indicated.

Truncated IgM is present in serum of old L−/− mice. (A) Level of μHC in serum of 2- to 14-month-old L−/− mice determined by ELISA at 1/100 dilution. (B) A comparative analysis of IgM serum titers in L−/− (▴), C-region deletion (CΔ26 ) as a negative control (♦) and normal (NM) mice (■). Means and standard deviation were calculated from the 10 L−/− mice in panel A and 7 NM mice. (C) Western analysis of serum antibodies from L−/−, of different age in months (m) as indicated. Sera from L−/−, μNR, and NM mice were purified by incubation with anti–mouse Ig coupled to Sepharose, separated on Ready-Gels under reducing conditions, and visualized with antibodies against mouse IgM. (D) Flow cytometric analysis of spleen cells surface-stained for IgM and B220. A representative presentation of a 1-year-old L−/− mouse compared with NM and μNRL−/− animals. The upper histograms show that, in addition to B220+ IgM+ cells, an IgMbright B220 population can be found in old L−/− mice. This population is more abundant in μNRL−/− mice. Plotting forward scatter (FSC) against IgM shows an IgMbright population of small particles with percentages indicated.

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