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RESEARCH PRODUCT
Microangiectasias: Structural regulators of lymphocyte transmigration
Moritz A. KonerdingSteven J. MentzerMei SuTimothy W. SecombCharles A. WestAlan J. Youngsubject
LymphocyteCellInflammationIn Vitro TechniquesBiologyMicrocirculationCell MovementCell AdhesionmedicineShear stressAnimalsLymphocytesCell adhesionMicrovesselInflammationMicroscopy VideoSheepMultidisciplinaryMicrocirculationHemodynamicsAdhesionBiological SciencesBiomechanical PhenomenaCell biologymedicine.anatomical_structureImmunologyMicroscopy Electron ScanningEndothelium Vascularmedicine.symptomdescription
The migration of lymphocytes into inflammatory tissue requires the migrating cell to overcome mechanical forces produced by blood flow. A generally accepted hypothesis is that these forces are overcome by a multistep sequence of adhesive interactions between lymphocytes and endothelial cells. This hypothesis has been recently challenged by results demonstrating wall shear stress on the order of 20 dyn/cm 2 in vivo and infrequent lymphocyte–endothelial adhesion at wall shear stress >1–2 dyn/cm 2 in vitro . Here, we show that lymphocyte slowing and transmigration in the skin is associated with microangiectasias, i.e., focal structural dilatations of microvessel segments. Microangiectasias are inducible within 4 days of the onset of inflammation and lead to a greater than 10-fold local reduction in wall shear stress. These findings support the hypothesis that a preparatory step to lymphocyte transmigration involves structural adaptations in the inflammatory microcirculation.
year | journal | country | edition | language |
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2003-06-02 | Proceedings of the National Academy of Sciences |