Multiscale imaging of corneal endothelium damage and effects of Rho Kinase inhibitor application in mouse models of acute ocular hypertension.
Zhen CaiYang ZhangRaymond S FangBenjamin BrennerJunghun KweonCheng SunJeffery GoldbergHao F ZhangPublished in: bioRxiv : the preprint server for biology (2023)
We developed a multiscale optical imaging workflow, integrating and correlating visible-light optical coherence tomography, confocal laser scanning microscopy, and single-molecule localization microscopy to investigate the mouse cornea damages from the in-vivo tissue level to the nanoscopic single-molecule level. We used electron microscopy to validate the imaged nanoscopic structures. We imaged wild-type mice and mice with acute ocular hypertension and examined the effects of Rho Kinase inhibitor application. We defined four types of intercellular tight junction structures as healthy, compact, partially-distorted, and fully-distorted types by labeling the Zonula occludens-1 protein in the corneal endothelial cell layer. We correlated the statistics of the four types of tight junction structures with cornea thickness and intraocular pressure. We found that the population of fully-distorted tight junctions correlated well with the level of cornea edema, and applying Rho Kinase inhibitor reduced the population of fully-distorted tight junctions under acute ocular hypertension.
Keyphrases
- single molecule
- high resolution
- optical coherence tomography
- liver failure
- wild type
- blood brain barrier
- blood pressure
- electron microscopy
- respiratory failure
- atomic force microscopy
- living cells
- optic nerve
- aortic dissection
- drug induced
- visible light
- protein kinase
- high speed
- endothelial cells
- smooth muscle
- high fat diet induced
- intensive care unit
- diabetic retinopathy
- photodynamic therapy
- hepatitis b virus
- metabolic syndrome
- binding protein
- mass spectrometry
- arterial hypertension
- type diabetes
- high throughput