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. 2025 Mar 14;11:24. doi: 10.1038/s41421-025-00782-4

Author Correction: Postsynaptic lncRNA Sera/Pkm2 pathway orchestrates the transition from social competition to rank by remodeling the neural ensemble in mPFC

Ling-Shuang Zhu 1,#, Chuan Lai 1,#, Chao-Wen Zhou 1,#, Hui-Yang Chen 1, Zhi-Qiang Liu 1, Ziyuan Guo 2, Hengye Man 3, Hui-Yun Du 1, Youming Lu 1, Feng Hu 4, Zhiye Chen 4, Kai Shu 4,, Ling-Qiang Zhu 1,, Dan Liu 1,
PMCID: PMC11909124  PMID: 40087265

Correction to: Cell Discovery (2024) 10(1):87 10.1038/s41421-024-00706-8, published online 20 August 2024

In the original publication of this article, we inadvertently replaced the Pkm2/AK018848/DAPI staining images for the IL region of the C4 mouse group in Supplementary Fig. S12d with incorrect images. These incorrect images were taken from the same brain slide as the Pkm1/AK018848/DAPI staining images for the PL region of the C1 mouse group in Supplementary Fig. S12c.

Additionally, while we typically apply the same parameters for imaging the same brain region and staining across different experimental groups (e.g., C1 and C4), the images in Supplementary Figs. S12c and S12d were processed with different parameters, resulting in noticeable discrepancies in fluorescence intensity and image scaling.

The correct Supplementary Fig. S12d is displayed as below. This correction does not affect the results or the conclusion of this work. We are sorry for any inconvenience that might cause.graphic file with name 41421_2025_782_Figa_HTML.jpg

Supplementary Fig. S12. AK018848 mediates alternative splicing of Pkm.

a LncRNA expression in mPFC of C1 and C4 mice detected by qPCR. n = 6.

b Representative double-immunofluorescence images with antibodies against CaMKII (turquoise) and FISH for AK016725, AK132182 or AK018848 (red) in PL. Bar = 30 μm.

c, d Representative double-immunofluorescence images with antibodies against Pkm1 or Pkm2 (turquoise) and FISH for AK018848 (red) in mPFC. Bar = 30 μm.

e Lack of difference in proportion of AK018848+ Cells. n = 6.

f Quantification for relative fluorescence intensity of AK018848 in PL. n = 6.

g Correlation of fluorescence intensity between AK018848 and Pkm1 or Pkm2.

h, i Relative mRNA levels of Pkm1 and Pkm2 via qPCR after AAV-CMV-AK018848-mCherry or AAV-CMV-si-AK018848-mCherry application on mouse hippocampal primary neurons. n = 6.

j, k Representative blots (up) and quantification (down) of Pkm1 and Pkm2 protein after AAV-CMV-AK018848-mCherry or AAV-CMV-si-AK018848-mCherry was applied on mouse hippocampal primary neurons. n = 6.

All data are shown as means ± SEM. For a, e and f, paired t-test was used. For hk, unpaired t-test was used. For g, simple linear regression was used. *P < 0.05, **P < 0.01, ***P < 0.001.

Contributor Information

Kai Shu, Email: kshu@tjh.tjmu.edu.cn.

Ling-Qiang Zhu, Email: zhulq@mail.hust.edu.cn.

Dan Liu, Email: liudan_echo@mail.hust.edu.cn.


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