Individual astrocyte morphology in the collagenous lamina cribrosa revealed by multicolor DiOlistic labeling

• Published in: Experimental eye research 2023-05, Vol.230, p.109458-109458, Article 109458
• Main Authors: Waxman, Susannah, Quinn, Marissa, Donahue, Cara, Falo, Louis D., Sun, Daniel, Jakobs, Tatjana C., Sigal, Ian A.
• Format: Article
• Language: English
• Subjects: Animals; Astrocyte; Astrocytes - metabolism; Glaucoma - metabolism; Humans; Lamina cribrosa; Microscopy; Morphology; Optic Disk; Optic nerve head; Retinal Ganglion Cells - metabolism; Sheep; Swine
• ISSN: 0014-4835; 1096-0007
• DOI: 10.1016/j.exer.2023.109458

Astrocytes in the lamina region of the optic nerve head play vital roles in supporting retinal ganglion cell axon health. In glaucoma, these astrocytes are implicated as early responders to stressors, undergoing characteristic changes in cell function as well as cell morphology. Much of what is currently known about individual lamina astrocyte morphology has been learned from rodent models which lack a defining feature of the human optic nerve head, the collagenous lamina cribrosa (LC). Current methods available for evaluation of collagenous LC astrocyte morphology have significant shortcomings. We aimed to evaluate Multicolor DiOlistic labeling (MuDi) as an approach to reveal individual astrocyte morphologies across the collagenous LC. Gold microcarriers were coated with all combinations of three fluorescent cell membrane dyes, DiI, DiD, and DiO, for a total of seven dye combinations. Microcarriers were delivered to 150 μm-thick coronal vibratome slices through the LC of pig, sheep, goat, and monkey eyes via MuDi. Labeled tissues were imaged with confocal and second harmonic generation microscopy to visualize dyed cells and LC collagenous beams, respectively. GFAP labeling of DiOlistically-labeled cells with astrocyte morphologies was used to investigate cell identity. 3D models of astrocytes were created from confocal image stacks for quantification of morphological features. DiOlistic labeling revealed fine details of LC astrocyte morphologies including somas, primary branches, higher-order branches, and end-feet. Labeled cells with astrocyte morphologies were GFAP+. Astrocytes were visible across seven distinct color channels, allowing high labeling density while still distinguishing individual cells from their neighbors. MuDi was capable of revealing tens to hundreds of collagenous LC astrocytes, in situ, with a single application. 3D astrocyte models allowed automated quantification of morphological features including branch number, length, thickness, hierarchy, and straightness as well as Sholl analysis. MuDi labeling provides an opportunity to investigate morphologies of collagenous LC astrocytes, providing both qualitative and quantitative detail, in healthy tissues. This approach may open doors for research of glaucoma, where astrocyte morphological alterations are thought to coincide with key functional changes related to disease progression. [Display omitted] •We demonstrate Multicolor DiOlistics (MuDi) for labeling individual astrocytes of col