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Author Spotlight: Ex Vivo OCT-Based Multimodal Imaging of Human Donor Eyes for Research into Age-Related Macular Degeneration
Published on: May 26, 2023
Comparison of histologic findings in age-related macular degeneration with RPE flatmount images
Qing Zhang1, Micah A Chrenek1, Shagun Bhatia1
1Department of Ophthalmology, Emory University School of Medicine, Atlanta, GA.
Purpose:
To visualize and analyze ex vivo flatmounted human RPE morphology from patients with age-related macular degeneration (AMD), and to compare the morphology with histologic findings. To establish whether the sub-RPE structures identified en face in RPE flatmount preparations are drusen with histopathological registration in serial sections. To detect characteristic patterns found en face in RPE with the same structures in histological cross sections from eyes from cadavers of patients with AMD.
Methods:
Twenty-eight postmortem eyes from 14 patients (16 eyes with AMD and 12 age-matched control eyes) were oriented and microdissected yielding a RPE-choroid preparation. The tissues were flatmounted, stained with Alexa Fluor 635 Phalloidin (AF635-phalloidin) for f-actin and propidium iodide for DNA, and imaged using confocal microscopy. Portions of tissue from macular regions were processed for electron microscopic examination. After confocal imaging, the samples were remounted for histologic processing, embedded in paraffin, and serially sectioned perpendicular to the plane of the RPE-choroid sheet. Scaled two-dimensional (2D) maps of drusen locations found with the histological cross sections were constructed and correlated with the en face confocal microscopic images.
Results:
Twenty-eight postmortem eyes with a mean time of death to tissue preservation of 23.7 h (range 8.0–51 h) from 14 donors (seven women and seven men) with an average age of 78 years (range 60–93 years) were evaluated. Eight donors had AMD, and six served as controls. Scattered small, hard drusen were present in the periphery of the eyes with AMD and the healthy eyes. The macular region of the eyes with AMD contained small (<63 µm), medium (63.0–124 µm), and large (125 µm) drusen. The RPE was arranged in rosette-like structures overlying small drusen, attenuated overlying medium-sized drusen, and consisted of large multinucleated cells overlying large drusen. The RPE in the area of geographic atrophy was attenuated and depigmented.
Conclusions:
Confocal images of flatmounts from eyes with AMD showed RPE patterns overlying various types of drusen and geographic atrophy that correlated with histologic characteristics. We propose RPE repair mechanisms that may result in the patterns that we observed.
Insights
This study visualizes retinal pigment epithelium (RPE) morphology in age-related macular degeneration (AMD) using flatmounts and histology, revealing distinct RPE patterns over drusen. These findings help understand AMD progression and RPE repair mechanisms.
Area of Science:
- Ophthalmology
- Histopathology
- Cell Biology
Background:
- Age-related macular degeneration (AMD) is a leading cause of vision loss.
- Understanding the morphology of the retinal pigment epithelium (RPE) in AMD is crucial for developing effective treatments.
- Current methods for analyzing RPE in AMD have limitations in visualizing complex structures.
Purpose of the Study:
- To visualize and analyze ex vivo human RPE morphology in AMD patients using flatmount preparations.
- To correlate en face RPE flatmount findings with histopathological features of drusen.
- To identify characteristic RPE patterns associated with AMD pathology.
Main Methods:
- Postmortem human eyes (16 with AMD, 12 controls) were used.
- Retinal pigment epithelium (RPE)-choroid preparations were flatmounted, stained, and imaged via confocal microscopy.
- Samples underwent serial sectioning for histopathological correlation with en face images.
Main Results:
- Distinct RPE patterns were observed overlying various drusen sizes in AMD eyes.
- RPE cells formed rosette-like structures over small drusen and multinucleated cells over large drusen.
- RPE in areas of geographic atrophy was attenuated and depigmented.
Conclusions:
- En face RPE flatmount imaging provides a detailed view of RPE morphology in AMD.
- Observed RPE patterns suggest active repair mechanisms in response to drusen and atrophy.
- This technique aids in understanding AMD pathogenesis and potential therapeutic targets.
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