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Updated: Jul 2, 2026

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Real-Time In Vitro Migration Assay for Primary Murine CD8+ T Cells
Published on: May 24, 2024
Assays of transendothelial migration in vitro
William A Muller1, F William Luscinskas
1Department of Pathology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Methods in Enzymology
|September 6, 2008
Summary
This study details reliable in vitro assays for observing leukocyte transendothelial migration, crucial for understanding inflammation and wound healing. These methods accurately predict in vivo inflammatory responses.
Area of Science:
- Immunology
- Cell Biology
- Physiology
Background:
- The inflammatory response is vital for healing and fighting pathogens, but uncontrolled inflammation underlies many diseases.
- Leukocyte recruitment and their migration across endothelium are key events in inflammation, often considered irreversible.
- Understanding leukocyte transendothelial migration is crucial for studying inflammatory processes.
Purpose of the Study:
- To describe established in vitro assays for studying leukocyte transendothelial migration.
- To provide reliable and reproducible methods for observing this critical cellular process.
- To validate these assays for predicting in vivo inflammatory responses.
Main Methods:
- Detailed description of in vitro transendothelial migration assays.
- Utilizing controlled laboratory conditions for observing leukocyte-endothelial cell interactions.
- Comparison of in vitro assay results with in vivo inflammation models.
Main Results:
- The described in vitro assays have been used successfully for decades.
- These methods demonstrate reproducibility, reliability, and predictive value.
- The assays accurately reflect leukocyte and endothelial cell behavior in inflammatory conditions in vivo.
Conclusions:
- In vitro transendothelial migration assays are powerful tools for dissecting inflammatory mechanisms.
- These assays offer a controlled environment to study leukocyte trafficking.
- The described methods are validated for their predictive relevance to in vivo inflammation.

