Correction: Immun Ageing 12, 23 (2015)
https://doi.org/10.1186/s12979-015-0050-z
Following publication of the original article [1], the authors identified an error in Fig. 1. All the images shown in Fig. 1 (from image A to I) are crops of larger images. To obtain the image G, we mistakenly used the source of the image A instead of the source of the image G. In this new version, the image G has been corrected. The legend of the image remains correct. The correct figure is given below.
Sera from SAMP8, ICR-CD1 and BALB/C mice contain anti-neo-epitope IgMs. Representative images of the hippocampal region of brain sections from 15-month-old ICR-CD1 mice simultaneously stained with Hoechst (blue), anti-MMP-2 antibody (green) and mouse sera (red) from each experimental group as detailed next. a-c: Sera from SAMP8 mice aged 1, 3 and 6 months, respectively. d-g: Sera from ICR-CD1 mice aged 1, 3, 6 and 9 months, respectively. h: Serum from a BALB/C mouse aged 3 months. i: Control staining of the granules with anti-neo-epitope IgMs contained in the OX52 antibody. In all cases the anti-MMP-2 staining showed the clusters of granules. Some granules of the clusters are stained with the serum, indicating that all sera contained anti-neo-epitope IgMs. Scale bar: 50 μm
Reference
Manich G, Augé E, Cabezón I, et al. Neo-epitopes emerging in the degenerative hippocampal granules of aged mice can be recognized by natural IgM auto-antibodies. Immun Ageing. 2015;12:23. https://doi.org/10.1186/s12979-015-0050-z.
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Manich, G., Augé, E., Cabezón, I. et al. Correction: Neo-epitopes emerging in the degenerative hippocampal granules of aged mice can be recognized by natural IgM auto-antibodies. Immun Ageing 19, 37 (2022). https://doi.org/10.1186/s12979-022-00293-w
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DOI: https://doi.org/10.1186/s12979-022-00293-w