CORRECTION article

Front. Aging Neurosci., 09 April 2025

Sec. Parkinson’s Disease and Aging-related Movement Disorders

Volume 17 - 2025 | https://doi.org/10.3389/fnagi.2025.1596878

Corrigendum: Boosting antioxidant self-defenses by grafting astrocytes rejuvenates the aged microenvironment and mitigates nigrostriatal toxicity in parkinsonian brain via an Nrf2-driven Wnt/β-catenin prosurvival axis

  • 1Pharmacology Section, Department of Biomedical and Biotechnological Sciences, Medical School, University of Catania, Catania, Italy
  • 2Section of Neuropharmacology, OASI Research Institute-IRCCS, Troina, Italy

A Corrigendum on
Boosting antioxidant self-defenses by grafting astrocytes rejuvenates the aged microenvironment and mitigates nigrostriatal toxicity in parkinsonian brain via an Nrf2-driven Wnt/β-catenin prosurvival axis

by Serapide, M. F., L'Episcopo, F., Tirolo, C., Testa, N., Caniglia, S., Giachino, C., and Marchetti, B. (2020). Front. Aging Neurosci. 12:24. doi: 10.3389/fnagi.2020.00024

In the published article, there was an error in Figure 4 as published. The image in Figure 4 A2 was erroneously selected and should have instead illustrated the time-course effect of MPTP ± tVM-AS paralleling striatal DAT-IF and TH-IF image analyses (B, C), DA uptake levels (D), and behavioral analyses (E). The corrected Figure 4 and its caption appear below.

Figure 4
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Figure 4. tVM-As grafts counteract MPTP-induced loss of DAergic innervation and synaptosomal dopamine (DA) uptake in the striatum, and revert Parkinson's disease (PD) motor deficits. (A1–A12) Representative confocal images of dopamine transporter (DAT, revealed in CY3, red)-fluorescence intensity (FI) and tyrosine hydroxylase (TH, revealed in FITC, green) showing the recognized loss of striatal DAT-IF and TH-IF 4 weeks post MPTP treatment compared to saline (A1–A4) as opposed to the ability of tVM-As to counteract MPTP-induced loss of DAT-IF and TH-IF at all time tested (A5–A12). DAT (B) and TH-(C) immunofluorescent staining measured by image analysis. Scale bars: 50 μm. (D) VM-As grafts increase high-affinity striatal (Str) DA uptake assessed by [3H]DA incorporation (mean % SEM). (E) Motor performances on rotarod showing recovery from motor impairment in MPTP/tVM-As but not MPTP/PBS mice. *p < 0.05, **p < 0.01 vs. saline/PBS; °p < 0.05, °°p < 0.01 vs. MPTP/PBS, at each time interval respectively, by ANOVA followed by post hoc Newman–Keuls test.

In the published article, there was an error in Figure 5 as published. The image in Figure 5 A2 was also erroneously selected. The corrected Figure 5 and its caption appear below.

Figure 5
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Figure 5. tVM-As downregulate microglial pro-inflammatory phenotype in SNpc. (A, B) tVM-As reverse MPTP-induced reactive microglial cells displaying the morphology of activated macrophage-like microglia (A1,A3) and the increased IBA1+/Dapi+ microglial cell numbers in midbrain sections at the level of the SNpc (B). Note the ramified microglia in SNpc of tVM-As mice (A2, A4). Scale bars: (A1, A2), 100 μm; (A3, A4), 25 μm. (C, D) SNpc tissues were processed for gene expression analyses of mRNA species using qRT-PCR. Values (AU, mean % SEM of n = 5 samples/experimental group) are expressed as fold changes. In MPTP/PBS, inflammatory (TNF-α, IL1-β, IL-6) mRNAs are upregulated by about 5- to 6-fold (p < 0.01) over saline-injected controls (C), whereas the anti-inflammatory cytokine IL-10 is not affected. Transplantation of VM-As in MPTP mice induced a significant (p < 0.01) downregulation of pro-inflammatory markers at all tps but increased IL-10 expression vs. MPTP/PBS (D). (E) Evaluation of IL-1β, TNF-α, IL-6, and IL-10 at a protein level, as determined by enzyme-linked immunosorbent assay (ELISA) in homogenate tissue samples (mean % SEM of n = 5 samples/experimental group), documents the ability of tVM-As to suppress the pro-inflammatory cytokines in the face of a significant increase in the anti-inflammatory cytokine, IL-10, when levels are compared to MPTP/PBS mice. *p < 0.05, **p < 0.01 vs. saline/PBS; °°p < 0.01 vs. MPTP/PBS; p < 0.01 vs. saline/PBS and MPTP/PBS, at each time interval respectively, by ANOVA with post hoc Newman–Keuls.

In the published article, in the section Results, subsection tVM-As Grafts Counteract MPTP-Induced Loss of DAergic Innervation and Synaptosomal DA Uptake in the Str and Revert PD Motor Deficits, paragraph two, a text correction is needed to comment on the corrected Figure 4.

This sentence previously stated:

“Hence, tVM-As grafts efficiently counteracted the MPTP-induced loss of striatal TH and DAT innervation (Figures 4A1–A3 and Figures 4B–C).”

The corrected sentence appears below:

“Hence, tVM-As grafts efficiently counteracted the MPTP-induced loss of striatal TH and DAT innervation (Figures 4A1–A12 and Figures 4B–C).”

The authors apologize for these errors and state that they do 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: Parkinson's disease, aging, astrocyte–neuron crosstalk, neuroinflammation, dopaminergic neurons, neuroprotection

Citation: Serapide MF, L'Episcopo F, Tirolo C, Testa N, Caniglia S, Giachino C and Marchetti B (2025) Corrigendum: Boosting antioxidant self-defenses by grafting astrocytes rejuvenates the aged microenvironment and mitigates nigrostriatal toxicity in parkinsonian brain via an Nrf2-driven Wnt/β-catenin prosurvival axis. Front. Aging Neurosci. 17:1596878. doi: 10.3389/fnagi.2025.1596878

Received: 20 March 2025; Accepted: 24 March 2025;
Published: 09 April 2025.

Edited and reviewed by: Alberto Javier Ramos, National Scientific and Technical Research Council (CONICET), Argentina

Copyright © 2025 Serapide, L'Episcopo, Tirolo, Testa, Caniglia, Giachino and Marchetti. 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: Bianca Marchetti, YmlhbmNhbWFyY2hldHRpQGxpYmVyby5pdA==

ORCID: Maria Francesca Serapide orcid.org/0000-0001-6332-4772
Francesca L'Episcopo orcid.org/0000-0003-3292-9677
Cataldo Tirolo orcid.org/0000-0003-1747-8134
Nunzio Testa orcid.org/0000-0002-4024-2325
Salvatore Caniglia orcid.org/0000-0002-9416-8458
Carmela Giachino orcid.org/0000-0003-3650-8677
Bianca Marchetti orcid.org/0000-0002-9287-8448

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.

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