Time course of angiopoietin-2 release during experimental human endotoxemia and sepsis 英文参考文献.docVIP
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Time course of angiopoietin-2 release during experimental human endotoxemia and sepsis 英文参考文献
Available online /content/13/3/R64
Research
Open Access
Vol 13 No 3
Time course of angiopoietin-2 release during experimental human
endotoxemia and sepsis
Philipp Kümpers1*, Matijs van Meurs2,3*, Sascha David1, Grietje Molema3, Johan Bijzet3,
Alexander Lukasz1, Frank Biertz4, Hermann Haller1 and Jan G Zijlstra2
1Department of Nephrology Hypertension, Hannover Medical School, Carl-Neuberg-Stra?e 1, 30625 Hannover, Germany
2Department of Critical Care, University Medical Center Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands
3Department of Pathology and Medical Biology, University Medical Center Groningen, Hanzeplein 19713 GZ Groningen, The Netherlands
4Department of Biometrics, Hannover Medical School, Carl-Neuberg-Stra?e 1, 30625 Hannover, Germany
* Contributed equally
Corresponding author: Philipp Kümpers, kuempers.philipp@mh-hannover.de
Received: 12 Feb 2009 Revisions requested: 3 Apr 2009 Revisions received: 21 Apr 2009 Accepted: 5 May 2009 Published: 5 May 2009
Critical Care 2009, 13:R64 (doi:10.1186/cc7866)
This article is online at: /content/13/3/R64
? 2009 Kümpers et al.; licensee BioMed Central Ltd.
This is an open access article distributed under the terms of the Creative Commons Attribution License (/licenses/by/2.0),
which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract
Introduction Endothelial activation leading to vascular barrier
breakdown denotes a devastating event in sepsis. Angiopoietin
(Ang)-2, a circulating antagonistic ligand of the endothelial
specific Tie2 receptor, is rapidly released from Weibel-Palade
and has been identified as a non-redundant gatekeeper of
endothelial activation. We aimed to study: the time course of
Ang-2 release during human experimental endotoxemia; the
association of Ang-2 with soluble adhesion molecules and
inflammatory cytokines; and the early time course of Ang-2
releas
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