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Microfluidic Flow Chambers Using Reconstituted Blood to Model Hemostasis and Platelet Transfusion In Vitro
Published on: March 19, 2016
In vitro interaction between cultured cells and human blood platelets
Thrombosis and Haemostasis
|August 31, 1978
Summary
Human cultured cells, including tumor and Chang liver cells, can trigger platelet aggregation. This process is primarily mediated by adenosine diphosphate (ADP), with potential involvement of coagulation factors.
Area of Science:
- Hematology
- Cell Biology
- Biochemistry
Background:
- Investigating the interaction between cultured human cells and blood platelets is crucial for understanding hemostasis and thrombosis.
- Previous studies suggest cell-derived factors can influence platelet function.
Purpose of the Study:
- To determine the effects of washed human cultured cells (tumor cells and Chang liver cells) on human blood platelets.
- To elucidate the mechanisms underlying cell-induced platelet aggregation.
Main Methods:
- Studied platelet aggregation in heparinized plasma induced by suspensions of cultured tumor cells and Chang liver cells.
- Performed ultrastructural examination of platelet aggregates.
- Analyzed washing fluids for the presence of adenosine diphosphate (ADP) and assessed the role of ADP using apyrase.
Main Results:
- Tumor cell suspensions induced significant platelet aggregation, characterized by tightly packed central aggregates with intact alpha-granules and peripheral aggregates showing organelle loss and fibrin strands.
- Washing fluids from tumor cells also induced aggregation, which was reversible by apyrase, indicating ADP mediation.
- Two of three Chang liver cell lines induced aggregation, correlating with detectable ADP in their washing fluids.
Conclusions:
- Cell-induced platelet aggregation is primarily mediated by adenosine diphosphate (ADP).
- A potential additional role for coagulation activity in platelet aggregation induced by certain cultured cells cannot be excluded.
- Variability exists among different cell lines (e.g., Chang liver cells) in their capacity to induce platelet aggregation.

