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Manipulating the Murine Lacrimal Gland
Published on: November 18, 2014
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Manipulating the murine lacrimal gland
Jennifer K Finley1, D'Juan Farmer1, Elaine Emmerson1
1Craniofacial and Mesenchymal Biology, Cell and Tissue Biology, University of California San Francisco.
Journal of Visualized Experiments : Jove
|December 10, 2014
Summary
This study details methods for dissecting and culturing the lacrimal gland (LG), crucial for tear production and eye health. These techniques aim to facilitate research into LG development and function.
Area of Science:
- Ophthalmology
- Developmental Biology
- Anatomy
Background:
- The lacrimal gland (LG) produces aqueous tears vital for corneal health and vision.
- LG development involves epithelial branching morphogenesis, a process less understood in LG compared to other glands.
- Difficulties in LG dissection and culture hinder research.
Purpose of the Study:
- To describe standardized dissection techniques for embryonic and post-natal lacrimal glands (LG).
- To present methods for ex vivo culture of lacrimal gland tissue.
- To facilitate further research into lacrimal gland morphogenesis and function.
Main Methods:
- Detailed dissection protocols for harvesting mouse lacrimal glands (LG) at embryonic and post-natal stages.
- Established ex vivo culture methods for maintaining lacrimal gland tissue viability and structure.
- Photographic documentation of dissection procedures.
Main Results:
- Successfully demonstrated reproducible techniques for isolating intact lacrimal glands (LG).
- Established protocols for successful ex vivo culture of lacrimal gland explants.
- Provided a foundational resource for studying lacrimal gland development.
Conclusions:
- The described methods overcome previous technical barriers in lacrimal gland (LG) research.
- These techniques will enable detailed investigation into the mechanisms of lacrimal gland morphogenesis.
- This work supports the lacrimal gland as a viable model for studying epithelial development.

