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.
Figure 3
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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Anna Sancho-Balsells1,2,3,4Veronica Brito1,2,3,4Belissa Fernández1,2,3,4Mónica Pardo2,3,4,5Marco Straccia2,3,4,5,6Silvia Ginés1,2,3,4Jordi Alberch1,2,3,4,6Isabel Hernández7Belén Arranz8Josep M. Canals2,3,4,5,6Albert Giralt1,2,3,4,6*
* 1Departament de Biomedicina, Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain
* 2Institut de Neurociències, Universitat de Barcelona, Barcelona, Spain
* 3Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain
* 4Centro de Investigación Biomédica en Red sobre Enfermedades Neurodegenerativas (CIBERNED), Madrid, Spain
* 5Laboratory of Stem Cells and Regenerative Medicine, Department of Biomedical Sciences, Faculty of Medicine and Health Science, University of Barcelona, Barcelona, Spain
* 6Faculty of Medicine and Health Science, Production and Validation Center of Advanced Therapies (Creatio), University of Barcelona, Barcelona, Spain
* 7Alzheimer Research Center and Memory Clinic, Fundació ACE, Institut Català de Neurociències Aplicades. Barcelona, Spain
* 8Parc Sanitari Sant Joan de Déu, CIBERSAM, Barcelona, Spain
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