Abstract
Disruption to barriers of the central nervous system (CNS) has been shown in both prime and drive pathologies observed across numerous neurological and ophthalmological conditions. These barriers are composed of well evolved endothelial tight junctions, and the key junctional component, claudin-5 (CLDN-5), is responsible for maintaining homeostasis of brain and retinal tissues. Indeed, decreased CLDN-5 expression has now been observed across many neurological and retinal diseases. Additionally, methods aimed at stabilising and upregulating CLDN-5 expression may have profound efficacy in treating a vast array of these conditions. However, very few targeted and specific methods can enhance CLDN-5 expression levels, and none of these have detailed its localisation and stability on the cell surface. In an effort to discover unknown and specific regulators of CLDN-5 expression, we performed a genome-wide cell-sorting-based phenotypic screen using CRISPR/Cas9. Sorting cells based on the phenotype of 'barrier tightness' revealed two candidate genes, EH domain-containing protein 4 (EHD4) and Arf-GAP with SH3 domain, ANK repeat, and PH domain-containing protein 2 (ASAP2), which, when suppressed, led to significant upregulation of CLDN-5 protein on the cell surface. EHD4 appeared to regulate the transcriptional activity of CLDN5, whereas ASAP2 controlled junctional localisation of CLDN-5. Identification of these candidate genes suggests that pharmacological inhibitors of EHD4 or ASAP2 may represent profound approaches to regulating CLDN-5 in neural endothelial cells.