Abstract

Objective- Pathological neovascularization is crucial for progression and morbidity of serious diseases such as cancer, diabetic retinopathy, and age-related macular degeneration. While mechanisms of ongoing pathological neovascularization have been extensively studied, the initiating pathological vascular remodeling (PVR) events, which precede neovascularization remains poorly understood. Here, we identify novel molecular and cellular mechanisms of preneovascular PVR, by using the adult choriocapillaris as a model. Approach and Results- Using hypoxia or forced overexpression of VEGF (vascular endothelial growth factor) in the subretinal space to induce PVR in zebrafish and rats respectively, and by analyzing choriocapillaris membranes adjacent to choroidal neovascular lesions from age-related macular degeneration patients, we show that the choriocapillaris undergo robust induction of vascular intussusception and permeability at preneovascular stages of PVR. This PVR response included endothelial cell proliferation, formation of endothelial luminal processes, extensive vesiculation and thickening of the endothelium, degradation of collagen fibers, and splitting of existing extravascular columns. RNA-sequencing established a role for endothelial tight junction disruption, cytoskeletal remodeling, vesicle- and cilium biogenesis in this process. Mechanistically, using genetic gain- and loss-of-function zebrafish models and analysis of primary human choriocapillaris endothelial cells, we determined that HIF (hypoxia-induced factor)-1α-VEGF-A-VEGFR2 signaling was important for hypoxia-induced PVR. Conclusions- Our findings reveal that PVR involving intussusception and splitting of extravascular columns, endothelial proliferation, vesiculation, fenestration, and thickening is induced before neovascularization, suggesting that identifying and targeting these processes may prevent development of advanced neovascular disease in the future. Visual Overview- An online visual overview is available for this article.

Highlights

  • Our findings reveal that pathological vascular remodeling (PVR) involving intussusception and splitting of extravascular columns, endothelial proliferation, vesiculation, fenestration, and thickening is induced before neovascularization, suggesting that identifying and targeting these processes may prevent development of advanced neovascular disease in the future

  • See cover image to clinically detectable masses,[2] growth and destabilization of atherosclerotic plaques before rupture,[3] synovitis and joint hypertrophy in rheumatoid arthritis,[4] macular edema, retinal detachment and vision loss in diabetic retinopathy (DR),[5] and Arterioscler Thromb Vasc Biol is available at https://www.ahajournals.org/journal/atvb

  • Α-smooth muscle actin age-related macular degeneration choroidal neovascularization diabetic retinopathy endothelial cell extracellular matrix endothelial luminal process fluorescence-activated cell sorting hypoxia-induced factor human TATA box-binding protein intussusceptive pillar prolyl hydroxylase domain pathological vascular remodeling retinal pigment epithelium smooth muscle cell transmission electron microscopy transgellin[1] vascular endothelial growth factor zonula occludens age-related macular degeneration (AMD)[6] all depend on pathological neovascularization

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Summary

Methods

The data that support the findings of this study are available from the corresponding author on reasonable request.Zebrafish Strains and Their MaintenanceTg(fli1a:EGFP)y1, Tg(kdrl:EGFP)s843, Tg(kdrl:DsRed2)pd[27], Tg(acta2:EGFP)ca[7], Tg(tagln:EGFP)p151, and Tg(gata1a:DsRed2) sd[2] transgenic strains[46,47,48,49,50,51] were obtained from ZIRC, Oregon. The data that support the findings of this study are available from the corresponding author on reasonable request. Tg(fli1a:EGFP)y1, Tg(kdrl:EGFP)s843, Tg(kdrl:DsRed2)pd[27], Tg(acta2:EGFP)ca[7], Tg(tagln:EGFP)p151, and Tg(gata1a:DsRed2) sd[2] transgenic strains[46,47,48,49,50,51] were obtained from ZIRC, Oregon. Ubs1855 transgenic strains were from the Affolter laboratory and the Tg(pdgfrb:mcitrine;kdrl:DsRed2),[56] Hif1aa−/−;Hif1ab−/−57 and Hsp70:VEGFAA-DN58 zebrafish lines were from the Stainier laboratory. All strains and double or triple transgenic crosses between these stains were maintained at the Zebrafish facility at Linköping University, Linköping, Sweden following standard protocols.[39,59] All the experimental procedures have been previously approved by the Linköping animal ethics committee.

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