Revisiting the role of Dcc in visual system development with a novel eye clearing method.

Abstract

The Deleted in Colorectal Carcinoma (Dcc) receptor plays a critical role in optic nerve development. Whilst Dcc is expressed postnatally in the eye, its function remains unknown as Dcc knockouts die at birth. To circumvent this drawback, we generated an eye-specific Dcc mutant. To study the organization of the retina and visual projections in these mice, we also established EyeDISCO, a novel tissue clearing protocol that removes melanin allowing 3D imaging of whole eyes and visual pathways. We show that in the absence of Dcc, some ganglion cell axons stalled at the optic disc, whereas others perforated the retina, separating photoreceptors from the retinal pigment epithelium. A subset of visual axons entered the CNS, but these projections are perturbed. Moreover, Dcc-deficient retinas displayed a massive postnatal loss of retinal ganglion cells and a large fraction of photoreceptors. Thus, Dcc is essential for the development and maintenance of the retina.

• Authors: Robin J Vigouroux, Quénol Cesar, Alain Chédotal, Kim Tuyen Nguyen-Ba-Charvet
• Journal: eLife (Elife) Vol. 9 (02 25 2020) ISSN: 2050-084X [Electronic] England
• PMID: 32096760 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2020, Vigouroux et al.

Chemical References

• DCC Receptor
• Dcc protein, mouse
• Melanins

Topics

• Animals
• DCC Receptor (genetics, physiology)
• Melanins (isolation & purification)
• Mice
• Mutation
• Retina (embryology, metabolism)
• Visual Pathways (physiology)