Aurin tricarboxylic acid self-protects by inhibiting aberrant complement activation at the C3 convertase and C9 binding stages

Lee, M; Guo, JP; Mcgeer, EG; Mcgeer, PL

HERO ID

2902681

Reference Type

Journal Article

Year

2013

Language

English

PMID

23177218

HERO ID 2902681
In Press No
Year 2013
Title Aurin tricarboxylic acid self-protects by inhibiting aberrant complement activation at the C3 convertase and C9 binding stages
Authors Lee, M; Guo, JP; Mcgeer, EG; Mcgeer, PL
Journal Neurobiology of Aging
Volume 34
Issue 5
Page Numbers 1451-1461
Abstract Aberrant complement activation is known to exacerbate the pathology in a spectrum of degenerative diseases of aging. We previously reported that aurin tricarboxylic acid (ATA) is an orally effective agent which prevents formation of the membrane attack complex of complement. It inhibits C9 attachment to tissue bound C5b678 and thus prevents bystander lysis of host cells. In this study, we investigated the effects of ATA on the alternative complement pathway. We found that ATA prevented cleavage of the tissue bound properdin-C3b-Factor B complex into the active C3 convertase enzyme properdin-C3b-Factor Bb. This inhibition was reversed by adding Factor D to the serum. Using enzyme-linked immunosorbent type assays, we established that ATA binds directly to Factor D and C9 but not to properdin or other complement proteins. We conclude that ATA, by inhibiting at two stages of the alternative pathway, might be a particularly effective therapeutic agent in conditions such as macular degeneration, paroxysmal nocturnal hemoglobinemia, and rheumatoid arthritis, in which activation of the alternative complement pathway initiates self damage.
Doi 10.1016/j.neurobiolaging.2012.10.023
Pmid 23177218
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English