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Defining epithelial cell dynamics and lineage relationships in the developing lacrimal gland.

Citation
Farmer, D. 'J. T., et al. “Defining Epithelial Cell Dynamics And Lineage Relationships In The Developing Lacrimal Gland.”. Development (Cambridge, England), pp. 2517-2528.
Author D'Juan T Farmer, Sara Nathan, Jennifer K Finley, Kevin Shengyang Yu, Elaine Emmerson, Lauren E Byrnes, Julie B Sneddon, Michael T McManus, Aaron D Tward, Sarah M Knox
Keywords development, Epithelia, Lacrimal gland, Single cell sequencing, Tubulogenesis
Abstract

The tear-producing lacrimal gland is a tubular organ that protects and lubricates the ocular surface. The lacrimal gland possesses many features that make it an excellent model in which to investigate tubulogenesis, but the cell types and lineage relationships that drive lacrimal gland formation are unclear. Using single-cell sequencing and other molecular tools, we reveal novel cell identities and epithelial lineage dynamics that underlie lacrimal gland development. We show that the lacrimal gland from its earliest developmental stages is composed of multiple subpopulations of immune, epithelial and mesenchymal cell lineages. The epithelial lineage exhibits the most substantial cellular changes, transitioning through a series of unique transcriptional states to become terminally differentiated acinar, ductal and myoepithelial cells. Furthermore, lineage tracing in postnatal and adult glands provides the first direct evidence of unipotent KRT5 epithelial cells in the lacrimal gland. Finally, we show conservation of developmental markers between the developing mouse and human lacrimal gland, supporting the use of mice to understand human development. Together, our data reveal crucial features of lacrimal gland development that have broad implications for understanding epithelial organogenesis.

Year of Publication
2017
Journal
Development (Cambridge, England)
Volume
144
Issue
13
Number of Pages
2517-2528
Date Published
12/2017
ISSN Number
1477-9129
DOI
10.1242/dev.150789
Alternate Journal
Development
PMID
28576768
PMCID
PMC5536870
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