Three-dimensional Imaging Coupled with Topological Quantification Uncovers Retinal Vascular Plexuses Undergoing Obliteration

Autor: Tzung K. Hsiai, Pierre J. Guihard, Kristina I. Boström, Lynn K. Gordon, Song Li, Alison Chu, Parinaz Abiri, Varun Gudapati, Jie Zheng, Kyung In Baek, Michel M. Sun, Xili Ding, Yichen Ding, Chih-Chiang Chang, Scott Meyer
Jazyk: angličtina
Rok vydání: 2021
Předmět:
0301 basic medicine
Primary and secondary plexus
Oncology and Carcinogenesis
Medicine (miscellaneous)
Hyperoxia
Retinal Neovascularization
Topology
01 natural sciences
Retina
Oxygen induced retinopathy
010309 optics
03 medical and health sciences
chemistry.chemical_compound
Mice
Imaging
Three-Dimensional

Pregnancy
0103 physical sciences
medicine
Animals
Oxygen-induced retinopathy
Pharmacology
Toxicology and Pharmaceutics (miscellaneous)

Plexus
Vascular connectivity
Retinal Vessels
Retinal
medicine.disease
Vertical sprouts
Mice
Inbred C57BL

Oxygen
Disease Models
Animal

030104 developmental biology
Microvascular Network
Three dimensional imaging
chemistry
Animals
Newborn

Light sheet fluorescence microscopy
Retinal vasculature
cardiovascular system
Female
Light-sheet fluorescence microscopy
Retinopathy
Research Paper
Zdroj: Theranostics, vol 11, iss 3
Theranostics
Popis: Introduction: Murine models provide microvascular insights into the 3-D network disarray seen in retinopathy and cardiovascular diseases. Light-sheet fluorescence microscopy (LSFM) has emerged to capture retinal vasculature in 3-D, allowing for assessment of the progression of retinopathy and the potential to screen new therapeutic targets in mice. We hereby coupled LSFM, also known as selective plane illumination microscopy, with topological quantification, to characterize the retinal vascular plexuses undergoing preferential obliteration. Method and Result: In postnatal mice, we revealed the 3-D retinal microvascular network in which the vertical sprouts bridge the primary (inner) and secondary (outer) plexuses, whereas, in an oxygen-induced retinopathy (OIR) mouse model, we demonstrated preferential obliteration of the secondary plexus and bridging vessels with a relatively unscathed primary plexus. Using clustering coefficients and Euler numbers, we computed the local versus global vascular connectivity. While local connectivity was preserved (p > 0.05, n = 5 vs. normoxia), the global vascular connectivity in hyperoxia-exposed retinas was significantly reduced (p < 0.05, n = 5 vs. normoxia). Applying principal component analysis (PCA) for auto-segmentation of the vertical sprouts, we corroborated the obliteration of the vertical sprouts bridging the secondary plexuses, as evidenced by impaired vascular branching and connectivity, and reduction in vessel volumes and lengths (p < 0.05, n = 5 vs. normoxia). Conclusion: Coupling 3-D LSFM with topological quantification uncovered the retinal vasculature undergoing hyperoxia-induced obliteration from the secondary (outer) plexus to the vertical sprouts. The use of clustering coefficients, Euler's number, and PCA provided new network insights into OIR-associated vascular obliteration, with translational significance for investigating therapeutic interventions to prevent visual impairment.
Databáze: OpenAIRE