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Tracing the glycogen cells with protocadherin 12 during mouse placenta development
S Bouillot1, C Rampon, E Tillet
1CEA-Grenoble, DRDC-DVE, Laboratoire de Développement et Vieillissement de l'Endothélium Inserm EMI-0219, Université J. Fourier EMI 02-19, 17 rue des Martyrs, 38054 Grenoble, Cedex 9, France.
Placenta
|November 5, 2005
Summary
Mouse placental glycogen cells (GC) originate from the ectoplacental cone and invade the decidua. These cells accumulate glycogen and provide energy, with their unique P-cadherin expression influencing migration.
Area of Science:
- Developmental Biology
- Reproductive Biology
- Cell Biology
Background:
- Glycogen cells (GC) are a trophoblast subtype in the mouse placenta that invade the decidua.
- Previous work identified protocadherin 12 (PCDH12) as a specific marker for GC.
Purpose of the Study:
- To investigate the origin of PCDH12-positive cells (GC).
- To characterize the fate of GC within maternal tissues.
- To understand the migratory properties and lineage of GC.
Main Methods:
- Embryonic staging from embryonic day (E) 7.5 to E17.5.
- Analysis of PCDH12 expression.
- Observation of glycogen accumulation and cell migration.
- Assessment of P-cadherin expression.
- Localization of GC within the decidua and maternal vasculature.
Main Results:
- PCDH12-positive GC originate from the central ectoplacental cone at E7.5.
- Glycogen accumulation begins at E10.5, with migration observed from the same stage.
- GC lack P-cadherin expression, potentially facilitating migration.
- GC reside near maternal vascular sinuses but do not integrate into the endothelium.
- By E17.5, decidual GC undergo lysis, forming glycogen-rich lacunae.
Conclusions:
- GC and spongiotrophoblasts represent distinct lineages.
- GC migration is influenced by the absence of P-cadherin.
- Decidual GC-derived lacunae may serve as an energy source late in gestation or during delivery.

