Glomerular basement membrane heparan sulfate in health and disease: A regulator of local complement activation.

Borza DB
Matrix Biol. 2017 57-58: 299-310

PMID: 27609404 · PMCID: PMC5026315 · DOI:10.1016/j.matbio.2016.09.002

The glomerular basement membrane (GBM) is an essential component of the glomerular filtration barrier. Heparan sulfate proteoglycans such as agrin are major components of the GBM, along with α345(IV) collagen, laminin-521 and nidogen. A loss of GBM heparan sulfate chains is associated with proteinuria in several glomerular diseases and may contribute to the underlying pathology. As the major determinants of the anionic charge of the GBM, heparan sulfate chains have been thought to impart charge selectivity to the glomerular filtration, a view challenged by the negligible albuminuria in mice that lack heparan sulfate in the GBM. Recent studies provide increasing evidence that heparan sulfate chains modulate local complement activation by recruiting complement regulatory protein factor H, the major inhibitor of the alternative pathway in plasma. Factor H selectively inactivates C3b bound to surfaces bearing host-specific polyanions such as heparan sulfate, thus limiting complement activation on self surfaces such as the GBM, which are not protected by cell-bound complement regulators. We discuss mechanisms whereby the acquired loss of GBM heparan sulfate can impair the local regulation of the alternative pathway, exacerbating complement activation and glomerular injury in immune-mediated kidney diseases such as membranous nephropathy and lupus nephritis.

Copyright © 2016 Elsevier B.V. All rights reserved.

MeSH Terms (16)

Agrin Animals Collagen Type IV Complement Activation Complement C3b Complement Factor H Gene Expression Regulation Glomerular Basement Membrane Glomerulonephritis, Membranous Heparitin Sulfate Humans Laminin Lupus Nephritis Membrane Glycoproteins Signal Transduction Static Electricity

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