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Cellular & Molecular Biology Letters logoLink to Cellular & Molecular Biology Letters
. 2024 Oct 28;29:133. doi: 10.1186/s11658-024-00648-9

Correction: Extracellular vesicles derived from CD4 + T cells carry DGKK to promote sepsis-induced lung injury by regulating oxidative stress and inflammation

Guo-wei Tu 1,#, Yi Zhang 2,#, Jie-fei Ma 3,#, Jun-yi Hou 1, Guang-wei Hao 1, Ying Su 1, Jing-chao Luo 1, Lulu Sheng 4,, Luo Z 1,3,5,6,
PMCID: PMC11520461  PMID: 39468453

Correction : Cellular & Molecular Biology Letters (2023) 28:24 10.1186/s11658-023-00435-y

Following publication of the original article [1], the authors identified a similarity between the image labeled “CLP + shNC” in Fig. 6C of their article and an image in another publication from their hospital (PubMed: 34616481, Figure 5a). Upon careful investigation, the authors discovered that the image in question had been incorrectly labeled. The error occurred unintentionally due to the fact that two research teams from hospital, both studying acute lung injury, were working in the same laboratory. This resulted in an accidental mislabeling of the H&E histopathology slides because of an incorrect slide number in the shared platform.

Fig. 6.

Fig. 6

DGKK knockdown attenuated tissue damage, oxidative stress, and inflammation in mice with CLP-induced lung injury. Mice with CLP were injected with virus carrying plasmid expressing shRNA control (shNC) and shRNA targeting DGKK (shDgkk). The elevation of Dgkk abundance at the A mRNA and B protein levels in CLP model mice was restored by DGKK RNAi. C H and E staining indicated that the severe lung injury in CLP model mice was restored by Dgkk RNAi (scale bar, 100 μm). D The severity of histological injury and plasma levels of E ALT, F AST, and G LDH in CLP model mice was restored by DGKK RNAi. The elevation of H ROS levels and I MDA content in CLP model mice was restored by DGKK RNAi. The reduction of J SOD and K GPX activities in CLP model mice was restored by Dgkk RNAi. The elevation of L DAG content and M PKC activity in CLP model mice was restored by Dgkk RNAi. N The elevation of BALF content of TNF-α, IL-1β, and IL-6 in CLP model mice was restored by Dgkk RNAi. O The shortened survival in CLP model mice was restored by Dgkk RNAi. Data are presented as mean ± SD. ***P < 0.001 versus control. ##P < 0.01, ###P < 0.001 versus CLP + shNC

The correct Fig. 6 is given below:

The authors re-examined the original samples and thoroughly reviewed the data, and they are confident that this mistake does not alter the overall conclusions of the article.

Footnotes

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Guo-wei Tu, Yi Zhang and Jie-fei Ma contributed equally to this article and are co-first authors.

Contributor Information

Lulu Sheng, Email: yl20111211856@sjtu.edu.cn.

Luo Z, Email: luo.zhe@zs-hospital.sh.cn.

Reference

  • 1.Tu GW, Zhang Y, Ma J, Hou J, Hao G, Su Y, Luo J, Sheng L, Luo Z. Extracellular vesicles derived from CD4+ T cells carry DGKK to promote sepsis-induced lung injury by regulating oxidative stress and inflammation. Cell Mol Biol Lett. 2023;28:24. 10.1186/s11658-023-00435-y. [DOI] [PMC free article] [PubMed] [Google Scholar]

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