Erratum to: Acta Neuropathol DOI 10.1007/s00401-015-1450-z

As a result of an error during digital processing of Figure 1a for publication, one of the immunofluorescence panels (GA175-GFP Nucleolin staining) was accidentally strongly altered in contrast and brightness. The corrected version of the figure is shown below. The authors apologize for any confusion caused by this error.

In the published article, the collaborators from the two institutions, German Consortium for Frontotemporal Lobar Degeneration and Bavarian Brain Banking Alliance, were incorrectly listed in article note. These names have been relocated to the Appendix section in the article now.

Figure 1a and the collaborators list have been amended in the published article.

Fig. 1
figure 1

Differential localization of intranuclear DPR inclusions in transduced primary neurons and in neurons of cases with C9orf72 mutation. Double immunofluorescence for different DPR proteins (green) and nucleolin (red), a marker for the nucleolus, in primary neurons (a) and in frontal cortex of cases with C9orf72 mutation (b). Nuclei are labeled with DAPI. Single confocal sections containing the nucleolus are shown. a Primary neurons transduced with lentivirus expressing either GFP-GR149, PR175-GFP, GA175-GFP or GP80-V5/His (DIV6 + 7). Note that poly-GR and poly-PR but not poly-GA intranuclear inclusions are localized in the nucleolus. Poly-GA forms mainly compact cytoplasmic inclusions. Poly-GP expression is mainly pan-nuclear and also cytosolic. b In cortical areas of cases with C9orf72 mutation neuronal intranuclear poly-GA, poly-GR and poly-GP inclusions are mostly localized adjacent to the nucleolus (red arrows) or less frequently randomly distributed (white arrows). No colocalization of DPR proteins with the nucleolus is observed. Scale bars represent 10 µm