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Preimplantation mouse embryos express a cell surface receptor for tissue-plasminogen activator
P M Carroll1, W G Richards, A L Darrow
1Department of Pharmacology, State University of New York at Stony Brook 11794-8651.
Summary
Tissue-plasminogen activator (t-PA) in mouse embryos is not produced by the embryo itself but binds to the embryo
Area of Science:
- Reproductive biology
- Developmental biology
- Biochemistry
Background:
- Tissue-plasminogen activator (t-PA) is a serine protease.
- t-PA has been observed intracellularly in oocytes and extracellularly in fertilized eggs.
Purpose of the Study:
- To investigate the source and nature of extracellular t-PA activity in preimplantation mouse embryos.
- To determine if embryos synthesize t-PA or bind it from the environment.
Main Methods:
- Analysis of t-PA activity in preimplantation embryos at different stages (2-cell, 4-cell, morula).
- Culturing morulae and assessing their ability to bind exogenous mouse t-PA.
- Northern blot analysis to detect t-PA mRNA in embryos.
- Testing binding specificity with urokinase-type plasminogen activator (u-PA) and human t-PA.
Main Results:
- Extracellular t-PA activity is bound to the surface of fertilized eggs.
- t-PA activity levels change during preimplantation development, peaking at the morula stage.
- Cultured morulae lack endogenous t-PA activity but can bind exogenous mouse t-PA.
- Preimplantation embryos do not express detectable t-PA mRNA.
- Binding is specific to mouse t-PA, dose-dependent, saturable, and does not require the active site.
Conclusions:
- The t-PA activity associated with preimplantation mouse embryos originates from the oviductal fluid, not embryonic synthesis.
- A specific t-PA-binding activity exists on the surface of preimplantation mouse embryos.
- This binding may localize and concentrate t-PA activity, influencing early embryonic development.