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Tenascin Mr 220,000 isoform expression correlates with corneal cell migration
A Kaplony1, D R Zimmermann, R W Fischer
1Laboratorium für Biochemie I, ETH-Zentrum, Zürich, Switzerland.
Summary
Chicken tenascin isoforms are differentially expressed during embryonic development. The ten220 isoform is closely linked to cell migration in the embryonic cornea, suggesting a role in facilitating this process.
Area of Science:
- Developmental Biology
- Extracellular Matrix Biology
- Molecular Biology
Background:
- Tenascin is an extracellular matrix glycoprotein involved in cell adhesion and migration.
- Chicken tenascin exists in three isoforms (ten220, ten200, ten190) generated by alternative splicing.
- Understanding tenascin isoform expression is crucial for comprehending developmental processes.
Purpose of the Study:
- To investigate the differential expression of chicken tenascin isoforms during embryonic development.
- To correlate tenascin isoform expression with specific developmental events, particularly cell migration.
- To characterize the molecular properties of cell migration-associated tenascin isoforms.
Main Methods:
- Development of specific monoclonal antibodies (mAb T17 for ten220, mAb T16 for all isoforms).
- Immunohistochemical analysis of tenascin isoform distribution in embryonic chicken tissues.
- Biochemical analysis of tenascin isoforms from tissue extracts.
Main Results:
- Ten220 expression strongly correlates with cell migration in the embryonic cornea, appearing before and disappearing after neural crest cell and fibroblast invasion.
- Ten190/200 isoforms are present in the corneal epithelium, lens, sclera, and remain near the endothelium and Bowman's membrane.
- A potential new tenascin isoform (Mr 210,000) was detected in brain extracts.
Conclusions:
- Tenascin isoform synthesis is tightly regulated during development.
- The ten220 isoform likely plays a functional role in facilitating cell migration.
- Alternative splicing of tenascin contributes to diverse functions during embryonic development.