Related Experiment Videos
Morphology of the murine optic nerve
Chr Albrecht May1, Elke Lütjen-Drecoll
1Department of Anatomy II, Friedrich Alexander University, Universitätstrasse 19, D-91054 Erlangen, Germany. atmay@anatomie.uni-erlangen.de
Investigative Ophthalmology & Visual Science
|July 2, 2002
Summary
The murine optic nerve (ON) lacks a lamina cribrosa and choroidal vascular supply, differing significantly from other species. These unique morphological features may influence optic nerve damage in glaucoma studies.
Area of Science:
- Ophthalmology
- Neuroscience
- Comparative Anatomy
Background:
- The optic nerve (ON) transmits visual information from the retina to the brain.
- Understanding the structural and vascular anatomy of the ON is crucial for studying optic neuropathies like glaucoma.
Purpose of the Study:
- To investigate the detailed morphology of the murine optic nerve.
- To characterize the vascular supply and glial composition of the mouse ON.
Main Methods:
- Light and electron microscopy were used to examine C57/Bl6 and BalbC mouse eyes.
- Microvascular casting and scanning electron microscopy visualized the ON vasculature.
- Immunohistochemistry identified glial fibrillary acidic protein (GFAP), connexin 43, carbonic anhydrase II, and collagen types I and III.
Main Results:
- The transition from nonmyelinated to myelinated ON occurred 0.6 mm behind the globe.
- A lamina cribrosa was absent; axons passed through a scleral hole with collagenous support.
- Elongated astrocytes, positive for GFAP, formed layers within the ON, replacing connective tissue beams.
- The nonmyelinated ON received arterial supply from the central retinal artery, with no contribution from choroidal vessels.
Conclusions:
- The mouse ON head exhibits unique features, notably the absence of a lamina cribrosa and choroidal vascular supply.
- These distinct anatomical characteristics in mice may impact the relevance of glaucoma models.
- Further research in glaucomatous mice is needed to ascertain the roles of the lamina cribrosa and choroidal vasculature in optic nerve damage.