Corrigendum: Lack of Helios during neural development induces adult schizophrenia-like behaviors associated with aberrant levels of the TRIF-recruiter protein WDFY1

In the published article, there was an error in the image used for Figure 3J as published. The corrected Figure 3J and its caption appear below.

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Figure 3. Characterization of schizophrenia-like phenotypes related to striatal function in He–/– mice. (A) The curve in graph depicts the body weight gain in both genotypes, He–/– and He+/+ mice from embryonic day 14.5 (E14.5) to postnatal day 28 (P28) (n = 3 He+/+ males and 4 He+/+ females, and 4 He–/– males and 4 He–/– females). (B) Time to jump out from the glass cylinder in 8-week-old He–/– and He+/+ mice (n = 4 He+/+ males and 4 He+/+ females, and 3 He–/– males and 4 He–/– females). (C) Locomotor activity in the open field was monitored for 25 min in He–/– and He+/+ mice (n = 6 He+/+ males and 5 He+/+ females, and 5 He–/– males and 6 He–/– females). After these 25 min, all mice received an injection of D-amphetamine sulfate (3 mg/kg) as indicated by the top arrow in the graph and the locomotor activity was subsequently monitored for additional 45 min. The induced locomotor activation in He+/+ (D) and He–/– (E) mice was evaluated by comparing representative covered distances from baseline and from treatment as depicted in gray in (C). (F) Locomotor activity in the open field was monitored for 25 min in He–/– and He+/+ mice (n = 8 He+/+ and 8 He–/–; 4 males an 4 females per genotype). After these 25 min, all mice received an injection of R-(-)-apomorphine (0.5 mg/kg) as indicated by the top arrow in the graph and the locomotor activity was subsequently monitored for additional 45 min. The induced locomotor activation in He+/+ (G) and He–/– (H) mice was evaluated by comparing representative covered distances from baseline and from treatment as depicted in gray in (F). (I) Representative images of a DiI-labeled medium spiny neuron (scale bar = 20 microns) and (J) representative medium spiny neuron dendrites from 8-weeks-old He+/+ and He–/– mice (scale bar = 3 microns). (K) Quantitative analysis showing dendritic spine density per micron of dendritic length from 8-week-old He+/+ and He–/– mice (n = 26 dendrites from 5 He+/+ mice, 2 males and 3 females, and 20 dendrites from 5 He–/– mice, 3 males and 2 females). (L) Density of each type of dendritic spine (stubby, thin, and mushroom) in dendrites of medium spiny neurons from (K) in He–/– and He+/+ mice. Total evaluated spines: 977 from He+/+ mice and 1088 from He–/– mice. Bars represent mean ± SEM. Data were analyzed by unpaired Student's t-test in (B, K), by paired Student's t-test in (D, E, G, H) and by two-way ANOVA in (A, C, F, L). **p < 0.01, ***p < 0.001 when compared with He+/+ mice in (A–C, F, K, L). *p < 0.05, **p < 0.01 when compared with baseline data in (D, E, G, H).

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.

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Keywords: hippocampus, putamen, cortex, FENS1, psychosis, negative symptoms, DISC1

Citation: Sancho-Balsells A, Brito V, Fernández B, Pardo M, Straccia M, Ginés S, Alberch J, Hernández I, Arranz B, Canals JM and Giralt A (2025) Corrigendum: Lack of Helios during neural development induces adult schizophrenia-like behaviors associated with aberrant levels of the TRIF-recruiter protein WDFY1. Front. Cell. Neurosci. 18:1542681. doi: 10.3389/fncel.2024.1542681

Received: 10 December 2024; Accepted: 18 December 2024;
Published: 07 January 2025.

Edited and reviewed by: Arturo Ortega, Center for Research and Advanced Studies of the National Polytechnic Institute, Mexico

Copyright © 2025 Sancho-Balsells, Brito, Fernández, Pardo, Straccia, Ginés, Alberch, Hernández, Arranz, Canals and Giralt. 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: Albert Giralt, YWxiZXJ0Z2lyYWx0JiN4MDAwNDA7dWIuZWR1

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