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Tissue-specific, temporal changes in cell adhesion to echinonectin in the sea urchin embryo
C A Burdsal1, M C Alliegro, D R McClay
1Department of Zoology, Duke University, Durham, North Carolina 27706.
Developmental Biology
|April 1, 1991
Summary
Echinonectin and hyalin are key adhesion proteins in sea urchin development. Primary mesenchyme cells lose adhesion to echinonectin during ingression, while ectodermal cells increase their affinity for it.
Area of Science:
- Developmental Biology
- Cell Adhesion
- Marine Biology
Background:
- Echinonectin, a dimeric glycoprotein, is present in the hyaline layer of developing sea urchin embryos.
- Both echinonectin and the protein hyalin support embryonic cell adhesion in vitro.
- Previous research indicated hyalin supports cell adhesion, prompting investigation into echinonectin's specific role.
Purpose of the Study:
- To investigate the specificity of cell-echinonectin interactions during sea urchin development.
- To determine if primary mesenchyme cells (PMCs) coordinate a loss of adhesion to echinonectin during ingression, similar to their interaction with hyalin.
- To analyze changes in cell adhesion to echinonectin in different embryonic cell types over time.
Main Methods:
- Utilized a centrifugal force-based adhesion assay to quantify cell-echinonectin interactions.
- Compared adhesion of micromeres, PMCs, presumptive ectoderm, and endoderm to echinonectin at different developmental stages.
- Employed monoclonal antibodies specific to echinonectin to assess its role in combined substrata adhesion.
Main Results:
- Micromeres demonstrated strong adhesion to echinonectin.
- PMCs showed reduced adhesion to echinonectin at the time of ingression, mirroring their decreased adhesion to hyalin.
- Presumptive ectoderm and endoderm exhibited no change in echinonectin adhesion during this period, though initial adhesion was lower compared to hyalin.
Conclusions:
- Echinonectin and hyalin function independently as adhesive substrates for sea urchin embryonic cells.
- PMCs decrease their affinity for echinonectin during ingression.
- Ectodermal cells later increase their affinity for echinonectin, suggesting dynamic changes in cell-substrate interactions during development.