Skip to Content
MoleculesMolecules
  • Correction
  • Open Access

11 February 2025

Correction: Hao et al. Phosphorylation of Akt by SC79 Prevents Iron Accumulation and Ameliorates Early Brain Injury in a Model of Experimental Subarachnoid Hemorrhage. Molecules 2016, 21, 325

,
,
,
,
and
1
Jiangsu Key Laboratory for Molecular Medicine, Medical School of Nanjing University, Nanjing 210093, China
2
Department of Vascular Surgery, the Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing 210008, China
*
Authors to whom correspondence should be addressed.

Author Name Correction

In the published publication [1], there was an error regarding the author name. We changed Jiang Yu to Yu Jiang.

Error in Figure

In the original publication [1], there was a mistake in Figure 3D as published. There were overlapping panels in Figure 3D’s SAH and SAH+vehicle panels. The corrected Figure 3 appears below.
Figure 3. SC79 administration after SAH largely rescues the impairment of Fe-S cluster biogenesis and alleviates the damage of neurons. (A) Western blot analysis for frataxin and ISCU. Upper panel: representative protein levels of frataxin and ISCU. Lower panel: quantitative data of the protein levels; (B) in-gel assay of aconitase activity. Upper panel: representative result. Lower panel: quantitative data of enzymatic activities; (C) enzymatic activity (upper panel) and Western blot (bottom panel) assays of XOD and CS; (D) representative slides of Nissl staining (left panel) and quantitative data (right panel) visualizing the neuronal cell outline and structure; and (E) alterations in brain water content. Data are expressed as mean ± SD (n = 8 in each group). * p < 0.05, *** p < 0.001 vs. sham group, # p < 0.05, ### p < 0.001 vs. SAH group. ISCU, Fe-S cluster scaffold protein; XOD, xanthine oxidase; CS, citrate synthase.
Figure 3. SC79 administration after SAH largely rescues the impairment of Fe-S cluster biogenesis and alleviates the damage of neurons. (A) Western blot analysis for frataxin and ISCU. Upper panel: representative protein levels of frataxin and ISCU. Lower panel: quantitative data of the protein levels; (B) in-gel assay of aconitase activity. Upper panel: representative result. Lower panel: quantitative data of enzymatic activities; (C) enzymatic activity (upper panel) and Western blot (bottom panel) assays of XOD and CS; (D) representative slides of Nissl staining (left panel) and quantitative data (right panel) visualizing the neuronal cell outline and structure; and (E) alterations in brain water content. Data are expressed as mean ± SD (n = 8 in each group). * p < 0.05, *** p < 0.001 vs. sham group, # p < 0.05, ### p < 0.001 vs. SAH group. ISCU, Fe-S cluster scaffold protein; XOD, xanthine oxidase; CS, citrate synthase.
Molecules 30 00823 g003
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Hao, S.; Song, C.; Shang, L.; Jiang, Y.; Qiao, T.; Li, K. Phosphorylation of Akt by SC79 Prevents Iron Accumulation and Ameliorates Early Brain Injury in a Model of Experimental Subarachnoid Hemorrhage. Molecules 2016, 21, 325. [Google Scholar] [CrossRef] [PubMed]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Article Metrics

Citations

Article Access Statistics

Multiple requests from the same IP address are counted as one view.