Int J Biol Sci 2022; 18(5):2181-2183. doi:10.7150/ijbs.71902 This issue

Erratum

Nicotinamide Riboside Enhances Mitochondrial Proteostasis and Adult Neurogenesis through Activation of Mitochondrial Unfolded Protein Response Signaling in the Brain of ALS SOD1G93A Mice: Erratum

Qi Zhou1*, Lei Zhu1*, Weiwen Qiu1*, Yue Liu2, Fang Yang2, Wenzhi Chen2, Renshi Xu Corresponding address

1. Department of Neurology, Jiangxi Provincial People's Hospital, Affiliated People's Hospital of Nanchang University, Nanchang 330006, Jiangxi, China
2. Department of Neurology, First Affiliated Hospital of Nanchang University, Nanchang 330006, Jiangxi, China
*These authors contributed equally to this work.

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Citation:
Zhou Q, Zhu L, Qiu W, Liu Y, Yang F, Chen W, Xu R. Nicotinamide Riboside Enhances Mitochondrial Proteostasis and Adult Neurogenesis through Activation of Mitochondrial Unfolded Protein Response Signaling in the Brain of ALS SOD1G93A Mice: Erratum. Int J Biol Sci 2022; 18(5):2181-2183. doi:10.7150/ijbs.71902. Available from https://www.ijbs.com/v18p2181.htm

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Corrected-article in Int J Biol Sci, Volume 16, 284

 

In our paper, there were mistakes in Figure 5D and Figure 6D, E. They should be corrected as follows.

 Figure 5 

NR treatment increased the proliferation of NSCs/NPCs in the brain of ALS SOD1G93A mice. Representative photomicrographs showed the immunostaining of vimentin (A cell proliferation marker; red) in the SVZ (A), SGZ (B), OB (C) at 120 days of four groups mice. Cell nuclei were counterstained with DAPI (blue). Yellow arrows indicated the colocalization of vimentin+ cell and DAPI. Bar graphs showed the analysis of vimentin+ cells in SVZ (D), SGZ (E), OB (F) regions. Scale bar: 40μm. Data were expressed as mean ± SEM of n=3 mice/group; *P<0.05, **P<0.01, ***P<0.001, **** P<0.0001.

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 Figure 6 

NR treatment extended the survival of newborn neurons in the brain of ALS SOD1G93A mice. Representative photomicrographs showed the immunostaining of DCX (A maker of newborn neuron; red) and DAPI (blue) in SVZ (A), SGZ (B), OB (C) regions at 120 days from four groups mice. Cell nuclei were counterstained with DAPI. Yellow arrows indicated the colocalization of DCX+ cell and DAPI. Bar graphs showed the quantitative analysis of DCX+ cells in SVZ (D), SGZ (E), OB (F) regions. Scale bar: 40μm. Data were expressed as mean ± SEM of n=3 mice/group; *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001.

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Author contact

Corresponding address Corresponding author: Prof. Renshi Xu, Email: xurenshiedu.cn or 13767015770com, Department of Neurology, Jiangxi Provincial People's Hospital, Affiliated People's Hospital of Nanchang University, Nanchang 330006, Jiangxi, China. Tel: +86 0791-88603798.


Published 2022-3-3