1995
DOI: 10.1111/j.1365-2249.1995.tb03601.x
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The kinetics and distribution of C9 and SC5b-9 in vivo: effects of complement activation

Abstract: SUMMARYMany diseases associated wilh complement activation are characterized by tissue deposition of components of the terminal complement complex (TCC). The ninth component of complement (C9) plays an important role in the cytolytic effects, and may contribute to the non-lethal cellregulating functions ofthe TCC [1]. In this study we examined the behaviour of radiolabelled human C9 and its soluble complexed form SC5b-9 in vivo in order to determine the effects of complement activation on its turnover, distrib… Show more

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Cited by 13 publications
(8 citation statements)
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“…It is unclear whether the lower SC5b-9 levels measured in this study represent reduced complement activation, and hence reduced SC5b-9 generation, or enhanced activation with consumption of the terminal complement components leading to reduced SC5b-9 formation. Intra-dialytic blood-membrane interactions are a major stimulus for complement activation in HD patients and the SC5b-9 molecule has a short half-life of approximately 40 min [22]. The pre-dialysis SC5b-9 levels measured in this study, therefore, are likely to represent the nadir and be more reflective of inter-dialytic SC5b-9 clearance and/or redistribution rather than dialysis associated complement activation per se.…”
Section: Discussionmentioning
confidence: 99%
“…It is unclear whether the lower SC5b-9 levels measured in this study represent reduced complement activation, and hence reduced SC5b-9 generation, or enhanced activation with consumption of the terminal complement components leading to reduced SC5b-9 formation. Intra-dialytic blood-membrane interactions are a major stimulus for complement activation in HD patients and the SC5b-9 molecule has a short half-life of approximately 40 min [22]. The pre-dialysis SC5b-9 levels measured in this study, therefore, are likely to represent the nadir and be more reflective of inter-dialytic SC5b-9 clearance and/or redistribution rather than dialysis associated complement activation per se.…”
Section: Discussionmentioning
confidence: 99%
“…A previous report demonstrating that mesothelial cells produce C3 and C4 in vitro (Tang et al, 2004) supports our observation that C3 and C4 present in the peritoneum might be mainly delivered from mesothelial cells. The large molecular size (>1000 kDa) of sC5b-9 also indicates that it is unlikely to be delivered from the host circulation (Greenstein et al, 1995;Mizutani et al, 2010;Young et al, 1993). These findings suggest that sC5b-9 detected in PDF is produced in the peritoneal cavity and is retained there.…”
Section: Discussionmentioning
confidence: 99%
“…Although anaphylatoxins bind to cells and are also rapidly inactivated in vivo, the terminal SC5b-9 complex is stable. The half-life in plasma is ∼1 h [40,41], but it is probably considerably longer in closed compartments. SC5b-9 enhances endothelial permeability in vitro and in vivo at a concentration of just a few micrograms per milliliter [27].…”
Section: Discussionmentioning
confidence: 99%