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Requirements for leukocyte transmigration via the transmembrane chemokine CX3CL1
Authors:Nicole Schwarz  Jessica Pruessmeyer  Franz M Hess  Daniela Dreymueller  Elena Pantaler  Anne Koelsch  Reinhard Windoffer  Matthias Voss  Alisina Sarabi  Christian Weber  Antonio S Sechi  Stefan Uhlig  Andreas Ludwig
Institution:1. Institute of Pharmacology and Toxicology, RWTH Aachen University, Pauwelsstr. 30, 52074, Aachen, Germany
2. Interdisciplinary Center for Clinical Research, RWTH Aachen University, 52074, Aachen, Germany
3. Institute of Physiology, RWTH Aachen University, 52074, Aachen, Germany
4. Institute for Molecular and Cellular Anatomy, RWTH Aachen University, 52074, Aachen, Germany
5. Institute for Immunology, Christian-Albrechts University, 24118, Kiel, Germany
6. Institute for Molecular Cardiovascular Research, RWTH Aachen University, Aachen, Germany
7. Institute for Biomedical Engineering–Cell Biology, RWTH Aachen University, 52074, Aachen, Germany
Abstract:The surface-expressed transmembrane CX3C chemokine ligand 1 (CX3CL1/fractalkine) induces firm adhesion of leukocytes expressing its receptor CX3CR1. After shedding by the disintegrins and metalloproteinases (ADAM) 10 and 17, CX3CL1 also acts as soluble leukocyte chemoattractant. Here, we demonstrate that transmembrane CX3CL1 expressed on both endothelial and epithelial cells induces leukocyte transmigration. To investigate the underlying mechanism, we generated CX3CR1 variants lacking the intracellular aspartate-arginine-tyrosine (DRY) motif or the intracellular C-terminus which led to a defect in intracellular calcium response and impaired ligand uptake, respectively. While both variants effectively mediated firm cell adhesion, they failed to induce transmigration and rather mediated retention of leukocytes on the CX3CL1-expressing cell layer. Targeting of ADAM10 led to increased adhesion but reduced transmigration in response to transmembrane CX3CL1, while transmigration towards soluble CX3CL1 was not affected. Thus, transmembrane CX3CL1 mediates leukocyte transmigration via the DRY motif and C-terminus of CX3CR1 and the activity of ADAM10.
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