Correction: Inflammation and neutrophil extracellular traps in cerebral cavernous malformation

Correction to: Cellular and Molecular Life Sciences (2022) 79:206 10.1007/s00018-022-04224-2

In the published article Fig. 1 contain error. The correction Fig. 1 is as follow.

Fig. 1.

RNA-Seq analysis showed increased expression of inflammation-related genes in brain microvascular endothelial cells from Ccm3^iECKO mice (CCM3) in acute and chronic CCM. A Schematic diagram of the experimental design of the transcriptomic study in acute and chronic CCM, comparing CCM3 mice and wild-type (WT) mice (n = 3 per group in acute CCM, n = 5 in chronic CCM). B RNA-Seq gene expression analysis of up-regulated genes showing the top 20 most enriched gene ontology (GO) terms in acute (left panel) and chronic (right panel) CCM. Immune-related GO terms are given in bold. *Regulation of extrinsic apoptotic signaling pathway via death domain receptors, **adaptive immune responses based on somatic recombination of immune receptors built from immunoglobulin superfamily domains, # protein-DNA complex subunit organisation. C Bar plots for the numbers of CCM-associated immune genes that were up-regulated or down-regulated (DEGs) in acute (left) and chronic (right) CCM. For definition of immune genes, see Methods. D Heatmap showing the expression levels (Z-score of regularized log (rlog)-transformed counts) of significantly up-regulated DEGs (p_adj < 0.05 & |log₂foldchange|> 0.5; blue: low; red: high) in both acute (upper panel) and chronic (lower panel) models. The first annotation column to the right indicates differential expression in log₂ fold changes (red: high; white: low). The second to seventh annotation columns indicates the DEGs associated with enriched immune-like GO terms (stated at the top of the figure) from over-representation analysis. Some of the genes labelled after annotation columns were discussed in the text

The original article has been updated.