meningeal tissues; meninges; periventricular brain tissue
CTX TNA2; CTX cells; 293 T
other disease animal model
TGF-beta/SMAD (promotes); fibrosis (promotes); ceRNA regulation (other); other pathway/process (promotes)
RT-qPCR; FISH / smFISH; Luciferase Reporter Assay; RNA Pull-Down; Bioinformatics Analysis; Transfection; IF (Immunofluorescence); Western Blot; In Vivo Animal Model; H&E Staining
circHIPK3 could be a key therapeutic target against post-IVH communicating hydrocephalus.
In rat IVH and thrombin-stimulated astrocyte models, circHIPK3 is up-regulated and promotes post-IVH communicating hydrocephalus by driving meningeal/periventricular fibrosis. Mechanistically, circHIPK3 sponges miR-30a-3p, increases ACT1(TRAF3IP2), activates TGF-beta1/Smad3 signaling, and promotes fibrotic proteins such as Col1 and alpha-SMA. Knockdown of circHIPK3 alleviates fibrosis, ventricular enlargement, and neurological dysfunction, supporting its potential as a therapeutic target.
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CircHIPK3 regulates TGF-beta1/smad3 signaling in communicating hydrocephalus after intraventricular hemorrhage by sponging miR-30a-3p via ACT1.
biological research