Institute of Cardiovascular Regeneration, Centre of Molecular Medicine, Goethe University, Frankfurt, Germany.
Faculty of Biological Sciences, Goethe University, Frankfurt, Germany.
EMBO Rep. 2022 Jun 7;23(6):e54157. doi: 10.15252/embr.202154157. Epub 2022 May 8.
Vascular integrity is essential for organ homeostasis to prevent edema formation and infiltration of inflammatory cells. Long non-coding RNAs (lncRNAs) are important regulators of gene expression and often expressed in a cell type-specific manner. By screening for endothelial-enriched lncRNAs, we identified the undescribed lncRNA NTRAS to control endothelial cell functions. Silencing of NTRAS induces endothelial cell dysfunction in vitro and increases vascular permeability and lethality in mice. Biochemical analysis revealed that NTRAS, through its CA-dinucleotide repeat motif, sequesters the splicing regulator hnRNPL to control alternative splicing of tight junction protein 1 (TJP1; also named zona occludens 1, ZO-1) pre-mRNA. Deletion of the hnRNPL binding motif in mice (Ntras ) significantly repressed TJP1 exon 20 usage, favoring expression of the TJP1α- isoform, which augments permeability of the endothelial monolayer. Ntras mice further showed reduced retinal vessel growth and increased vascular permeability and myocarditis. In summary, this study demonstrates that NTRAS is an essential gatekeeper of vascular integrity.
血管完整性对于器官稳态至关重要,可防止水肿形成和炎症细胞浸润。长链非编码 RNA(lncRNA)是基因表达的重要调节剂,通常以细胞类型特异性方式表达。通过筛选富含内皮细胞的 lncRNA,我们鉴定了未描述的 lncRNA NTRAS 来控制内皮细胞功能。沉默 NTRAS 可诱导体外内皮细胞功能障碍,并增加小鼠的血管通透性和致死率。生化分析表明,NTRAS 通过其 CA 二核苷酸重复基序,隔离剪接调节剂 hnRNPL,以控制紧密连接蛋白 1(TJP1;也称为封闭蛋白 1,ZO-1)前体 mRNA 的可变剪接。在小鼠中删除 hnRNPL 结合基序(Ntras)可显著抑制 TJP1 外显子 20 的使用,有利于 TJP1α-异构体的表达,从而增加内皮单层的通透性。Ntras 小鼠进一步显示视网膜血管生长减少,血管通透性增加和心肌炎。总之,这项研究表明 NTRAS 是血管完整性的重要守门员。