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Verfasst von:Beck, Grietje [VerfasserIn]   i
 Ludwig, F. [VerfasserIn]   i
 Schulte, Jutta [VerfasserIn]   i
 Ackern, Klaus van [VerfasserIn]   i
 Woude, Fokko J. van der [VerfasserIn]   i
 Yard, Benito A. [VerfasserIn]   i
Titel:Fractalkine is not a major chemoattractant for the migration of neutrophils across microvascular endothelium
Verf.angabe:G. Ch Beck, F. Ludwig, J. Schulte, K. van Ackern, F.J. van der Woude & B.A. Yard
Jahr:2003
Umfang:8 S.
Fussnoten:First published: 21 July 2003 ; Gesehen am 24.06.2022
Titel Quelle:Enthalten in: Scandinavian journal of immunology
Ort Quelle:Oxford [u.a.] : Wiley-Blackwell, 1972
Jahr Quelle:2003
Band/Heft Quelle:58(2003), 2, Seite 180-187
ISSN Quelle:1365-3083
Abstract:Inflammatory responses during sepsis are determined by leucocyte recruitment into inflamed tissues. Both chemokines and adhesion molecules are believed to be involved in this process. As fractalkine exists as transmembrane protein with cell adhesion properties and as soluble chemotactic factor, the present study was conducted to study the role of fractalkine, produced by microvascular and macrovascular endothelial cells, in neutrophil recruitment. Lung microvascular endothelial cells (LMVECs) stimulated with lipopolysaccharide, tumour necrosis factor-alpha or interleukin-1 (IL-1) produced much more fractalkine compared with the macrovascular human umbilical vein endothelial cells (HUVECs). No differences were found between microvascular endothelial cells of different organs. Chemotactic activity in supernatants was significantly stronger in stimulated LMVEC when compared with HUVEC. Although recombinant fractalkine induced migration of neutrophils, IL-8 and monocyte chemoattractant protein-1 were found to be more strictly required. In vivo fractalkine was strongly upregulated in septic lung and kidney. Our data suggest that fractalkine production per se does not explain the preference for inflammation in the lung of septic patients.
DOI:doi:10.1046/j.1365-3083.2003.01298.x
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext: https://doi.org/10.1046/j.1365-3083.2003.01298.x
 Volltext: https://onlinelibrary.wiley.com/doi/full/10.1046/j.1365-3083.2003.01298.x
 DOI: https://doi.org/10.1046/j.1365-3083.2003.01298.x
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Chemokine CX3CL1
 Chemokines, CX3C
 Chemotaxis, Leukocyte
 Endothelium, Vascular
 Flow Cytometry
 Humans
 Immunohistochemistry
 Membrane Proteins
 Nephritis
 Neutrophils
 Pneumonia
 Reverse Transcriptase Polymerase Chain Reaction
 RNA
 Sepsis
 Up-Regulation
K10plus-PPN:1807797872
Verknüpfungen:→ Zeitschrift

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