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CORRECTION article

Front. Cell. Neurosci., 23 August 2023
Sec. Cellular Neurophysiology

Corrigendum: Polysialic acid promotes remyelination in cerebellar slice cultures by Siglec-E-dependent modulation of microglia polarization

  • 1Clinic for Neurology, Hannover Medical School, Hannover, Germany
  • 2Center for Systems Neuroscience Hannover, Hannover, Germany
  • 3Institute of Clinical Biochemistry, Hannover Medical School, Hannover, Germany
  • 4Translational Medicine, Novartis Institute for Biomedical Research, Novartis, Basel, Switzerland

A corrigendum on
Polysialic acid promotes remyelination in cerebellar slice cultures by Siglec-E-dependent modulation of microglia polarization

by Schröder, L.-J., Thiesler, H., Gretenkort, L., Möllenkamp, T. M., Stangel, M., Gudi, V., and Hildebrandt, H. (2023). Front. Cell. Neurosci. 17:1207540. doi: 10.3389/fncel.2023.1207540

In the published article, there was an error in Figure 6 as published. In panel A, the micrographs in columns 2 and 3 were labeled incorrectly. The corrected Figure 6 and its caption appear below.

FIGURE 6
www.frontiersin.org

Figure 6. PolySia DP24–30 has no direct impact on OPC differentiation. (A) Representative images of primary rat OPC cultures stained for A2B5 (magenta) and GALC (green) after 2 days of in vitro differentiation in the presence of polySia DP8–14 or polySia DP24–30, as indicated. Nuclear counterstain with DAPI (blue). Scale bars, 50 μm. (B–D) Absolute cell numbers per frame (B), and relative numbers of A2B5 (C) or GALC-positive cells (D). Data represent individual values and means ± SEM of n = 9–11 independent OPC cultures per condition. OPCs were obtained from overall three OPC pools prepared from eight neonatal rats, each. Per OPC culture well, 15–20 frames (150 × 200 μm) were evaluated. The one-way-ANOVA revealed significant differences (P < 0.0001 for GALC; P = 0.0223 for A2B5), and Tukey's post hoc tests were applied. Significant group differences are indicated (*P < 0.05; ****P < 0.0001).

The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Keywords: multiple sclerosis, organotypic cerebellar slice culture, remyelination, polysialic acid (polySia), Siglec-E, microglia, neuroinflammation, immunomodulation

Citation: Schröder L-J, Thiesler H, Gretenkort L, Möllenkamp TM, Stangel M, Gudi V and Hildebrandt H (2023) Corrigendum: Polysialic acid promotes remyelination in cerebellar slice cultures by Siglec-E-dependent modulation of microglia polarization. Front. Cell. Neurosci. 17:1275048. doi: 10.3389/fncel.2023.1275048

Received: 09 August 2023; Accepted: 11 August 2023;
Published: 23 August 2023.

Edited and reviewed by: Shirin Hosseini, Technical University of Braunschweig, Germany

Copyright © 2023 Schröder, Thiesler, Gretenkort, Möllenkamp, Stangel, Gudi and Hildebrandt. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Herbert Hildebrandt, aGlsZGVicmFuZHQuaGVyYmVydCYjeDAwMDQwO21oLWhhbm5vdmVyLmRl

These authors have contributed equally to this work and share first authorship

These authors have contributed equally to this work and share last authorship

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.