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α4-integrin-VCAM-1 binding mediates G protein–independent capture of encephalitogenic T cell blasts to CNS white matter microvessels
Peter Vajkoczy, … , Melanie Laschinger, Britta Engelhardt
Peter Vajkoczy, … , Melanie Laschinger, Britta Engelhardt
Published August 15, 2001
Citation Information: J Clin Invest. 2001;108(4):557-565. https://doi.org/10.1172/JCI12440.
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Article

α4-integrin-VCAM-1 binding mediates G protein–independent capture of encephalitogenic T cell blasts to CNS white matter microvessels

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Abstract

Direct in vivo evidence is still lacking for α4-integrin–mediated T cell interaction with VCAM-1 on blood-brain barrier–endothelium in experimental autoimmune encephalomyelitis (EAE). To investigate a possible α4-integrin–mediated interaction of encephalitogenic T cell blasts with VCAM-1 on the blood-brain barrier white matter endothelium in vivo, we have developed a novel spinal cord window preparation that enabled us to directly visualize CNS white matter microcirculation by intravital fluorescence videomicroscopy. Our study provides the first in vivo evidence that encephalitogenic T cell blasts interact with the spinal cord white matter microvasculature without rolling and that α4-integrin mediates the G protein–independent capture and subsequently the G protein–dependent adhesion strengthening of T cell blasts to microvascular VCAM-1.

Authors

Peter Vajkoczy, Melanie Laschinger, Britta Engelhardt

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Figure 6

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Localization of T lymphoblasts within the spinal cord parenchyma in cont...
Localization of T lymphoblasts within the spinal cord parenchyma in control animals. Six hours after infusion of T lymphoblasts, the Cell Tracker Orange–labeled T cell blasts (red fluorescence) could be localized outside the spinal cord microvasculature (green fluorescence) within the spinal cord parenchyma of control animals. Superimposed fluorescence is shown, which demonstrates one T cell blast attached within the venule (yellow fluorescence) and one T cell blast within the spinal cord parenchyma (red fluorescence). Bar, 10 μm.

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ISSN: 0021-9738 (print), 1558-8238 (online)

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