Skip to main content

Correction: Endomucin selectively regulates vascular endothelial growth factor receptor-2 endocytosis through its interaction with AP2

The Original Article was published on 11 April 2024

Correction: Cell Commun Signal 22, 225 (2024)

https://doi.org/10.1186/s12964-024-01606-w

Following publication of the original article [1], the authors reported an error in the additional file. The incorrect additional file was published. The correct file is published in this correction article and the original article [1] has been corrected.

Reference

  1. Cano I, Wild M, Gupta U, et al. Endomucin selectively regulates vascular endothelial growth factor receptor-2 endocytosis through its interaction with AP2. Cell Commun Signal. 2024;22:225. https://doi.org/10.1186/s12964-024-01606-w.

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Zhengping Hu.

Additional information

Publisher’s Note

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

The online version of the original article can be found at https://doi.org/10.1186/s12964-024-01606-w.

Electronic supplementary material

Below is the link to the electronic supplementary material.

12964_2024_1696_MOESM1_ESM.pdf

Additional file 1: Supplemental Fig. 1. Markov Clustering of EMCN-binding proteins identified by mass spectrometry. (A) EMCN-binding proteins identified through mass spectrometry were analyzed and visualized using the STRING database (https://string-db.org/). The network type was set to physical subnetwork, and the significance of network edges was based on confidence, with a minimum required interaction score of high confidence (0.700). Further functional clustering of EMCN-binding proteins was performed using Markov clustering. Proteins within the same cluster were connected by solid lines and marked with the same color, while dashed lines indicated boundaries between clusters. (B) The table lists the top five protein clusters with the highest number of proteins. Supplemental Fig. 2. Confirmation of EMCN knockdown. (A) Representative image of the western blot assay showing significant reduction of EMCN at protein level in HRECs transfected with siEMCN compared to siNT control. (B) Quantification of EMCN protein by western blot analysis demonstrates a significant decrease of EMCN at 72 h after transfection. Student-t test was used. ****P < 0.0001, n = 3. (C) Quantification of EMCN mRNA indicates a significant decrease of EMCN (1.024 ± 0.126 vs. 0.0128 ± 0.0003) at 48 h after transfection. Student-t test was used. ****P < 0.0001, n = 3.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Cano, I., Wild, M., Gupta, U. et al. Correction: Endomucin selectively regulates vascular endothelial growth factor receptor-2 endocytosis through its interaction with AP2. Cell Commun Signal 22, 311 (2024). https://doi.org/10.1186/s12964-024-01696-6

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/s12964-024-01696-6