In the original article, we neglected to include the funder “CAMS Innovation Fund for Medical Sciences (CIFMS), 2019-I2M-1-004” to Xiaolong Qi.
“This project was supported by the National Natural Science Foundation of China (81771413, 82001268, and 81771412) and Beijing Natural Science Foundation Program and the Scientific Research Key Program of the Beijing Municipal Commission of Education (KZ201810025041). Xuanwu Hospital Science Program for Fostering Young Scholars (QNPY2020005). The present work was supported in part by the CAMS Innovation Fund for Medical Sciences (CIFMS) (2017-I2M-3-015; 2019-I2M-1-004 to XQ).”
Also there was a mistake in Figure 3–5 as published. The word “rat” was miswritten as “mice.” The corrected Figure 3–5 appears below.
FIGURE 3
MiR-29a knockout enhanced infarct volume and edema volume in MCAO rats after day 3. (A) Coronal sections representing infarcts in wild-type rats and miR-29a knockout rats. (B) Bar graph calculating the infarct volume. (C) Bar graphs for calculating brain edema volume. (D) Bar graph for calculating rat body weight. Data represent mean ± SEM. n = 6 per group.*p < 0.05 compared to control. MCAO, middle cerebral artery occlusion.
FIGURE 4
Knockout of miR-29a exhibited M1 polarization of microglia in rat brain. (A,B) Western blot detection of microglia M1 and M2 marker changes in the brains of wild-type rats and miR-29a-5p knockout rats. (A) CD206, iNOS (B) Arg1, CD16. (C–F) Bar graphs of marker changes in the brains of wild-type rats and miR-29a knockout rats. (C) CD206, (D) Arg1, (E) CD16, (F) iNOS. (G,H) Representative double immunofluorescence staining for CD206 (green) or iNOS (green), and Iba-1 (red) markers. (G) CD206, (H) iNOS. *p < 0.05. Arg1, arginase 1; iNOS, inducible nitric oxide synthase.
FIGURE 5
MiR-29a knockout promoted astrocyte proliferation and increased the release of the neurotoxic substance glutamate in basal ganglia of rats after MCAO. (A) Detection of protein expression of GFAP in the brains of wild-type rats and miR-29a knockout rats by western blot. The next band corresponds to GFAP. (B) Bar graphs of protein expression of GFAP in the brains of wild-type and miR-29a knockout rats. (C) Bar graphs of Glu in the brains of wild-type rats and miR-29a knockout rats. Data represent mean ± SEM. n = 6 per group. *p < 0.05. GFAP, glial fibrillary acidic protein; Glu, glutamic acid.
Finally, there was an error in authorship. Xiaolong Qi was not included as an author in the published article. Authorlist has been corrected and his contribution has been added to the “Author Contributions.” The corrected statement appears below.
“FZ wrote the manuscript. HZ, JF, RW, ZH, ZT, YZ, FY, YH, LY, XZ, and LZ took part in the experiment and modified it. YL and YM designed and critically revised the manuscript. XQ did the construction work of miR-29a genetic modified rats All authors contributed to the article and approved the submitted version.”
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.
Statements
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.
Summary
Keywords
ischemic stroke, miR-29a, microglia, astrocyte, glutamate
Citation
Zhao F, Zhao H, Fan J, Wang R, Han Z, Tao Z, Zheng Y, Yan F, Huang Y, Yu L, Zhang X, Qi X, Zhang L, Luo Y and Ma Y (2021) Corrigendum: MiR-29a Knockout Aggravates Neurological Damage by Pre-polarizing M1 Microglia in Experimental Rat Models of Acute Stroke. Front. Genet. 12:738582. doi: 10.3389/fgene.2021.738582
Received
09 July 2021
Accepted
05 October 2021
Published
26 October 2021
Volume
12 - 2021
Edited and reviewed by
Yaohui Tang, Shanghai Jiao Tong University, China
Updates
Copyright
© 2021 Zhao, Zhao, Fan, Wang, Han, Tao, Zheng, Yan, Huang, Yu, Zhang, Qi, Zhang, Luo and Ma.
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: Yumin Luo, yumin111@ccmu.edu.c; Yuanwu Ma, mayuanwu@cnilas.org
†These authors share first authorship
This article was submitted to Neurogenomics, a section of the journal Frontiers in Genetics
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.