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Updated: Jan 27, 2026

Flow Cytometry Analysis of Tissue Factor Expression in Human Platelets
Published on: November 22, 2024
[PLATELETS FUNCTION IN A DROP OF BLOOD: FLOW CYTOMETRY ANALYSIS COMPARED TO PLATELET AGGREGATION].
Hagit Hauschner1,2, Tamar Katz1, Roy Beigel3
1Hemophilia National Center and the Institute of Thrombosis and Hemostasis, Sheba Medical Center, Tel Hashomer, Israel.
Flow cytometry (FC) offers a valuable alternative to light transmission aggregometry (LTA) for assessing platelet function, requiring less blood and not depending on platelet count. This method aids in diagnosing platelet disorders and evaluating anti-platelet drug responses.
Area of Science:
- Hematology
- Clinical Diagnostics
- Pharmacology
Background:
- Light transmission aggregometry (LTA) is the standard for diagnosing platelet function disorders but has limitations.
- LTA requires substantial blood volumes and a normal platelet count, restricting its use in certain patient populations.
Purpose of the Study:
- To compare flow cytometric (FC) platelet function testing with LTA.
- To evaluate FC in diverse groups: general population, patients on anti-platelet drugs, and neonates (term and preterm).
Main Methods:
- Platelet function assessed using LTA and FC with PAC1 binding and p-selectin expression as activation markers.
- Comparison in a patient receiving Clopidogrel (before and after loading).
- Analysis of platelet activation markers in term and preterm neonatal cord blood.
Main Results:
- ADP-induced platelet aggregation correlated with FC-assayed p-selectin expression (r=0.79-0.86).
- Both LTA and FC demonstrated Clopidogrel response at 72 hours, but not 24 hours post-loading.
- Preterm neonates showed reduced ADP-induced platelet activation (p-selectin reached significance).
Conclusions:
- FC analysis of platelet function is valuable for diagnosing impaired function and anti-platelet drug response.
- FC allows testing with minimal blood volume and independent of platelet count.
- Identifying specific activation markers for each agonist is crucial for FC analysis.
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