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CORRECTION article

Front. Immunol., 21 September 2021
Sec. Inflammation

Corrigendum: The GABAA Receptor Influences Pressure Overload-Induced Heart Failure by Modulating Macrophages in Mice

Jin Bu&#x;Jin Bu1†Shiyuan Huang&#x;Shiyuan Huang2†Jue WangJue Wang3Tong XiaTong Xia2Hui LiuHui Liu2Ya YouYa You2Zhaohui Wang*Zhaohui Wang2*Kun Liu*Kun Liu4*
  • 1Department of Pediatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 2Department of Geriatrics, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 3Department of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China
  • 4Institution of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China

A Corrigendum on
The GABAA Receptor Influences Pressure Overload-Induced Heart Failure by Modulating Macrophages in Mice

by Bu J, Huang S, Wang J, Xia T, Liu H, You Y, Wang Z and Liu K (2021). Front. Immunol. 12:670153. doi: 10.3389/fimmu.2021.670153

In the original article, there was a mistake in Figure 3A and Supplement 3 as published. In the Figure 3A, the bicuculine group at day 28 post-TAC was inadvertently saved in the improper folders and attached to Sham group at days 14 and 28 post-TAC, so the representative images of Sham group at days 14 and 28 post-TAC were wrong and duplicated. In the Supplement 3, the representative image of Sham group at day 21 post-TAC was chosen by mistake. The corrected Figure 3A and Supplement 3 appear below.

FIGURE 3
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Figure 3 Activation or blockade of the GABAA receptor selectively increases or reduces the number of Ly6Clow macrophages in the hearts of pressure-overload hypertrophy mice. Macrophage (CD45+F4/80+CD11b+) subpopulations were respectively defined as Ly6Chigh or Ly6Clow macrophages according to Ly-6C expression levels. (A) Representative images of Ly6Chigh and Ly6Clow macrophages at days 7, 14, and 28 post-TAC. The representative images of 1, 3, and 21 days after TAC were shown in supplementary materials. (B) The number of Ly6Clow macrophages or Ly6Chigh macrophages (per mg heart tissue) among the total number of live cells isolated from hearts at the indicated time points after TAC. (C) The number of CD45+CD11b+F4/80+EdU+cell (per mg heart tissue) among the total number of live cells isolated from hearts at the indicated time points after TAC. (D) Representative images of Ki-67+ expression in Ly6Clow macrophages at day 7 post-TAC. (E) The percentage of Ki-67+ expression in Ly6Clow macrophages. Data show the mean ± SEM, by one-way ANOVA with Bonferroni’s multiple comparison test. For topiramate treatment, *P < 0.05 vs. vehicle. For bicuculline treatment, #P < 0.05 vs. vehicle. (n = 3 mice for sham group, n = 6–8 mice for all other groups).

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.

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.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fimmu.2021.753404/full#supplementary-material

Supplement 3 | Living cells (upper panel) were gated to determine the presence of CD45+Ly6G-CD11b+Ly6Chigh and CD45+Ly6G-CD11b+Ly6Clow monocytes at day 21 post-TAC in the peripheral blood.

Keywords: GABAA receptor, amphiregulin, macrophage, monocyte, pressure-overload hypertrophy

Citation: Bu J, Huang S, Wang J, Xia T, Liu H, You Y, Wang Z and Liu K (2021) Corrigendum: The GABAA Receptor Influences Pressure Overload-Induced Heart Failure by Modulating Macrophages in Mice. Front. Immunol. 12:753404. doi: 10.3389/fimmu.2021.753404

Received: 04 August 2021; Accepted: 24 August 2021;
Published: 21 September 2021.

Edited and reviewed by:

Guochang Hu, University of Illinois at Chicago, United States

Copyright © 2021 Bu, Huang, Wang, Xia, Liu, You, Wang and Liu. 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: Zhaohui Wang, zhaohuiwang@hust.edu.cn; Kun Liu, liukun@hust.edu.cn

†These authors share first authorship

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.