Correction: Cell Commun Signal 22, 225 (2024)
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.
Electronic supplementary material
Below is the link to the electronic supplementary material.
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.
Footnotes
The online version of the original article can be found at 10.1186/s12964-024-01606-w.
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Patricia A. D’Amore and Zhengping Hu are co-senior authors.
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. 10.1186/s12964-024-01606-w. [DOI] [PMC free article] [PubMed]
Associated Data
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Supplementary Materials
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.