نتایج جستجو برای: complement c1 inhibitor proteins

تعداد نتایج: 779838  

Journal: :Circulation 2008
Erdenechimeg Shagdarsuren Kiril Bidzhekov Yassin Djalali-Talab Elisa A Liehn Mihail Hristov Robert A Matthijsen Wim A Buurman Alma Zernecke Christian Weber

BACKGROUND Although activation of the complement system has been implicated in the progression of human atherosclerosis, its function during arterial remodeling after injury has not been investigated. Here, we examined the contribution of the complement cascade to neointima formation in apolipoprotein E-deficient mice using a C1-esterase inhibitor (C1-inhibitor). METHODS AND RESULTS Apolipopr...

Journal: :Blood 1993
B J de Smet J P de Boer J Agterberg G Rigter W K Bleeker C E Hack

C1-inhibitor is the only known inhibitor of the classical pathway of complement and the major inhibitor of the contact pathway of coagulation. Like other serine proteinase inhibitors, C1-inhibitor can exist in three conformations, ie, the native, the proteinase-complexed, and the proteolytically inactivated form. Here we studied the plasma elimination kinetics of these three forms of human C1-i...

Journal: :European surgical research. Europaische chirurgische Forschung. Recherches chirurgicales europeennes 2004
D Inderbitzin G Beldi I Avital G Vinci D Candinas

Activation of the classical complement pathway is crucially involved in complement-mediated endothelial cell damage in ischemia-reperfusion injury. C1 inhibitor is the only known physiological inhibitor of classical complement pathway activation. Transgenic mice overexpressing human C1 inhibitor were used in a surgical lower torso and a liver ischemia-reperfusion model. Organ-specific endotheli...

Journal: :The Biochemical journal 1979
R B Sim G J Arlaud M G Colomb

The interaction of C1 inhibitor with complement component C1 bound to immune complexes was examined by using 125I-labelled C1 subcomponents. The inhibitor binds rapidly to subcomponent C1s, and more slowly to subcomponent C1r. Formation of the C1r-C1 inhibitor complex causes rapid dissociation of subcomponents C1r and C1s from the antibody-antigen-component C1 aggregate. The rate and extent of ...

Journal: :The Journal of clinical investigation 1976
M M Hurst J E Volanakis R M Stroud J C Bennett

The purpose of this study was to examine the molecular parameters necessary for initiation of complement fixation by IgM proteins. To determine why some IgM molecules are capable of complement fixation while others are not, several different Waldenström IgM proteins were examined for their ability to fix total hemolytic complement in the CH(50) assay. Subsequently, the C1 fixing ability of a 56...

Journal: :Annals of the rheumatic diseases 1991
S Nakamura M Yoshinari Y Saku K Hirakawa C Miishima K Murai K Tokiyama M Fujishima

A 22 year old woman with systemic lupus erythematosus affecting the central nervous system had acquired C1 inhibitor deficiency. She was admitted for treatment of psychotic behaviour, but showed no signs of angioedema. The serum complement profile of the patient showed normal C3 concentration and a depletion of C4, C2, C1 inhibitor, and C1q. Her parents had normal complement profiles. An extrem...

Journal: :Clinical and experimental immunology 2013
A Landsem E W Nielsen H Fure D Christiansen J K Ludviksen J D Lambris B Østerud T E Mollnes O-L Brekke

Both the complement system and tissue factor (TF), a key initiating component of coagulation, are activated in sepsis, and cross-talk occurs between the complement and coagulation systems. C1-inhibitor (C1-INH) can act as a regulator in both systems. Our aim in this study was to examine this cross-talk by investigating the effects of C1-INH on Escherichia coli-induced haemostasis and inflammati...

2014
Jonathan Levy Georges-Etienne Rivard Eric Wagner Don Beezhold Noam Berlin Li Fan Zhao Zhang Gordon L Sussman

BACKGROUND Angioedema (AE) is idiopathic in the majority of cases. We studied patients with AE for genetic variants of proteins involved with bradykinin generation and biodisposition. METHODS One hundred sixty one patients with AE were recruited at a university hospital clinic. Patients were categorized according to the proposed pathogenesis of AE: low C1 inhibitor (C1-INH) and C4 levels, aut...

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