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Characterization of a developmentally regulated mouse embryonic antigen
1Department of Biological Sciences, State University of New York, Albany 12222.
Summary
Embryonic cell surface glycoprotein (ESGp) expression changes during mouse development, with different molecular weights indicating specific cell types. ESGp may play a role in cell adhesion during early embryonic development.
Area of Science:
- Developmental Biology
- Cell Biology
- Glycoprotein Characterization
Background:
- Mammalian embryonic cell surface glycoprotein (ESGp) expression is developmentally regulated.
- ESGp's biochemical structure varies with embryonic stage and cell type.
- Previous studies suggest ESGp's involvement in cell-cell interactions.
Purpose of the Study:
- To isolate and characterize the developmentally regulated embryonic cell surface glycoprotein (ESGp).
- To investigate the molecular weight variations of ESGp during mouse embryogenesis.
- To determine the cell-type specific expression of ESGp in blastocysts and related cell lines.
Main Methods:
- Electrophoretic analyses to determine molecular weights of ESGp.
- Studies using embryonal carcinoma (EC) cells to differentiate molecular forms.
- Survey of various mouse tissues and cell lines for ESGp expression.
Main Results:
- ESGp presents as a 90 kDa molecule in early cleavage stages (2-8 cell) and morula embryos.
- At the blastocyst stage, ESGp appears as a heterogeneous band (90-110 kDa), composed of three distinct molecules (90, 95, 105-110 kDa).
- Specific molecular weights correlate with distinct cell types: 90 kDa (embryonic ectoderm), 95 kDa (visceral endoderm), and 110 kDa (parietal endoderm/differentiated cells).
Conclusions:
- ESGp exhibits distinct molecular forms associated with specific cell types during mouse embryonic development.
- ESGp expression is polarized to cell-cell contact areas in cultured EC cells, suggesting a role in adhesion.
- ESGp likely mediates intercellular adhesion in both embryonal carcinoma cells and compacting embryos.