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Cited by 313Systemic Lupus Erythematosus ResearchRenal Diseases and GlomerulopathiesVasculitis and related conditions

The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.

In vitro demonstration of a particular affinity of glomerular basement membrane and collagen for DNA. A possible basis for a local formation of DNA-anti-DNA complexes in systemic lupus erythematosus.

Open access
Izui, S, Lambert, P H, Miescher, P A·1976·The Journal of experimental medicine
DOI 10.1084/jem.144.2.428PMC PMC2190380
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Abstract

In vitro, collagen and collagen-like material in GBM, were demonstrated to have a particular high affinity for any DNA tested (mammalian, bacterial, viral, and plant). GBM fixed DNA 40-80 times more than HGG and BSA and 10-40 times more than bacterial LPS. GBM has a higher affinity for SSDNA than for DSDNA. This binding was inhibited at low pH, low ionic strength, and in the presence of anionic detergents, indicating that the highly negatively charged DNA may interact with the basic site on collagen or GBM by electrostatic forces. This interaction was competitively interfered with by DNA-binding proteins such as Clq. Complexes formed of DNA and anti-DNA antibodies did not exhibit the same binding property as free DNA. However, DNA which was already bound to GBM or to collagen could very efficiently bind anti-DNA antibodies and form immune complexes which would remain on these structures. The biological significance of the binding of DNA to GBM or to collagen should be particularly considered in relation to the pathogenesis of SLE. It is possible that DNA released from disrupted or degenerating cells would bind to surrounding collagen fibers or to basement membranes and then act as an immunoabsorbant for circulating anti-DNA antibodies. Some evidence for an in vivo binding of SSDNA to renal structures was obtained in mice treated with bacterial LPS 2 days before the injection of SSDNA.

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Metadata

Authors
Izui, S., Lambert, P. H., & Miescher, P. A.
Affiliations
World Health Organization (CH)
Venue
The Journal of experimental medicine
Publisher
Rockefeller University Press
Published
1976-08-01
Volume
144
Issue
2
Pages
428-443
ISSN
  • 0022-1007 (ISSN-L)
  • 1540-9538
DOI
10.1084/jem.144.2.428
PMC
PMC2190380
OpenAlex
W2085459553
Cited by
313
References
43
Citations by year
2026: 1 · 2025: 3 · 2024: 3 · 2021: 1 · 2020: 2 · 2019: 2 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 2
FWCI
19.18
Type
journal article
Language
en
Open access
Locations
  • The Journal of Experimental Medicine (publishedVersion)
  • PubMed Central (publishedVersion, cc-by-nc-sa)
  • PubMed (publishedVersion)
  • The Mouseion at the JAXlibrary (Jackson Laboratory) (submittedVersion)
  • Archive ouverte UNIGE (University of Geneva) (submittedVersion, cc-by)
  • Archive ouverte UNIGE (University of Geneva) (submittedVersion)
Funders
  • World Health Organization
  • National Research Foundation
Topics
  • Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
  • Health Sciences › Medicine › Nephrology › Renal Diseases and Glomerulopathies
  • Health Sciences › Medicine › Rheumatology › Vasculitis and related conditions
Keywords
glomerular basement membrane, collagen, DNA binding, anti-DNA antibodies, immune complexes, systemic lupus erythematosus, single-stranded DNA, electrostatic binding, C1q, lipopolysaccharide, lupus pathogenesis
MeSH terms
Animals, Antigen-Antibody Complex, Basement Membrane, Binding Sites, Collagen, Complement C1, DNA, DNA, Single-Stranded, Humans, Hydrogen-Ion Concentration, Kidney Glomerulus, Lupus Erythematosus, Systemic, Osmolar Concentration, Protein Binding, Solubility, Temperature, Mice

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