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Neonatal Wnt-dependent Lgr5 positive stem cells are essential for uterine gland development.
- Source :
-
Nature communications [Nat Commun] 2019 Nov 26; Vol. 10 (1), pp. 5378. Date of Electronic Publication: 2019 Nov 26. - Publication Year :
- 2019
-
Abstract
- Wnt signaling is critical for directing epithelial gland development within the uterine lining to ensure successful gestation in adults. Wnt-dependent, Lgr5-expressing stem/progenitor cells are essential for the development of glandular epithelia in the intestine and stomach, but their existence in the developing reproductive tract has not been investigated. Here, we employ Lgr5-2A-EGFP/CreERT2/DTR mouse models to identify Lgr5-expressing cells in the developing uterus and to evaluate their stem cell identity and function. Lgr5 is broadly expressed in the uterine epithelium during embryogenesis, but becomes largely restricted to the tips of developing glands after birth. In-vivo lineage tracing/ablation/organoid culture assays identify these gland-resident Lgr5 <superscript>high</superscript> cells as Wnt-dependent stem cells responsible for uterine gland development. Adjacent Lgr5 <superscript>neg</superscript> epithelial cells within the neonatal glands function as essential niche components to support the function of Lgr5 <superscript>high</superscript> stem cells ex-vivo. These findings constitute a major advance in our understanding of uterine development and lay the foundations for investigating potential contributions of Lgr5 <superscript>+</superscript> stem/progenitor cells to uterine disorders.
- Subjects :
- Animals
Cell Lineage
Endometrium growth & development
Female
Gene Expression Regulation, Developmental
Mice, Transgenic
Mullerian Ducts cytology
Organoids
Pregnancy
Receptors, G-Protein-Coupled genetics
Wnt Proteins genetics
Receptors, G-Protein-Coupled metabolism
Stem Cells cytology
Stem Cells physiology
Uterus growth & development
Wnt Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 10
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 31772170
- Full Text :
- https://doi.org/10.1038/s41467-019-13363-3