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CXCL1/CXCL8 (GROα/IL-8) in human diabetic ketoacidosis plasma facilitates leukocyte recruitment to cerebrovascular endothelium in vitro

Omatsu, Tatsushi; Cepinskas, Gediminas; Clarson, Cheril; Patterson, Eric K.; Alharfi, Ibrahim M.; Summers, Kelly; Couraud, Pierre-Olivier; Romero, Ignacio A.; Weksler, Babette and Fraser, Douglas D. (2014). CXCL1/CXCL8 (GROα/IL-8) in human diabetic ketoacidosis plasma facilitates leukocyte recruitment to cerebrovascular endothelium in vitro. American Journal of Physiology. Endocrinology and Metabolism, 306(9) E1077-E1084.

DOI (Digital Object Identifier) Link: https://doi.org/10.1152/ajpendo.00659.2013
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Abstract

Diabetic ketoacidosis (DKA) in children is associated with intracranial vascular complications, possibly due to leukocyte-endothelial interactions. Our aim was to determine whether DKA-induced inflammation promoted leukocyte adhesion to activated human cerebrovascular endothelium. Plasma was obtained from children with type 1 diabetes either in acute DKA or in an insulin-controlled state (CON). Plasma concentrations of 21 inflammatory analytes were compared between groups. DKA was associated with altered circulating levels of ↑CXCL1 (GROα), ↑CXCL8 (IL-8), ↑IL-6, ↑IFNα2, and ↓CXCL10 (IP-10) compared with CON. These plasma analyte measurements were then used to create physiologically relevant cytokine mixtures (CM). Human cerebral microvascular endothelial cells (hCMEC/D3) were stimulated with either plasma (DKA-P or CON-P) or CM (DKA-CM or CON-CM) and assessed for polymorphonuclear leukocyte (PMN) adhesion. Stimulation of hCMEC/D3 with DKA-P or DKA-CM increased PMN adhesion to hCMEC/D3 under "flow" conditions. PMN adhesion to hCMEC/D3 was suppressed with neutralizing antibodies to CXCL1/CXCL8 or their hCMEC/D3 receptors CXCR1/CXCR2. DKA-P, but not DKA-CM, initiated oxidative stress in hCMEC/D3. Expression of ICAM-1, VCAM-1, and E-selectin were unaltered on hCMEC/D3 by either DKA-P or DKA-CM. In summary, DKA elicits inflammation in children associated with changes in circulating cytokines/chemokines. Increased CXCL1/CXCL8 instigated PMN adhesion to hCMEC/D3, possibly contributing to DKA-associated intracranial vascular complications.

Item Type: Journal Item
Copyright Holders: 2014 the American Physiological Society
ISSN: 1522-1555
Keywords: CXC chemokine ligand; growth-regulated oncogene-α; pediatric; diabetes; ketoacidosis; cell trafficking; neutrophils; chemokines
Academic Unit/School: Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
Item ID: 42436
Depositing User: Ignacio A Romero
Date Deposited: 14 Apr 2015 08:40
Last Modified: 07 Dec 2018 10:29
URI: http://oro.open.ac.uk/id/eprint/42436
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