학술논문

Modulation of heparan sulfate in the glomerular endothelial glycocalyx decreases leukocyte influx during experimental glomerulonephritis.
Document Type
article
Source
Kidney international. 86(5)
Subject
Kidney Glomerulus
Leukocytes
Cell Line
Glycocalyx
Endothelial Cells
Animals
Mice
Inbred C57BL
Mice
Knockout
Anti-Glomerular Basement Membrane Disease
Disease Models
Animal
Sulfotransferases
Heparitin Sulfate
L-Selectin
Chemokines
Autoantibodies
Coculture Techniques
Transfection
Cell Adhesion
Signal Transduction
Chemotaxis
Leukocyte
Down-Regulation
RNA Interference
Time Factors
Female
Male
acute kidney injury
anti-GBM disease
endothelium
glomerular endothelial cells
glomerular filtration barrier
glomerulonephritis
glycocalyx
heparan sulfate
Mice
Inbred C57BL
Knockout
Disease Models
Animal
Chemotaxis
Leukocyte
Clinical Sciences
Urology & Nephrology
Language
Abstract
The glomerular endothelial glycocalyx is postulated to be an important modulator of permeability and inflammation. The glycocalyx consists of complex polysaccharides, the main functional constituent of which, heparan sulfate (HS), is synthesized and modified by multiple enzymes. The N-deacetylase-N-sulfotransferase (Ndst) enzymes initiate and dictate the modification process. Here we evaluated the effects of modulation of HS in the endothelial glycocalyx on albuminuria and glomerular leukocyte influx using mice deficient in endothelial and leukocyte Ndst1 (TEKCre+/Ndst1flox/flox). In these mice, glomerular expression of a specific HS domain was significantly decreased, whereas the expression of other HS domains was normal. In the endothelial glycocalyx, this specific HS structure was not associated with albuminuria or with changes in renal function. However, glomerular leukocyte influx was significantly reduced during antiglomerular basement membrane nephritis, which was associated with less glomerular injury and better renal function. In vitro decreased adhesion of wild-type and Ndst1-deficient granulocytes to Ndst1-silenced glomerular endothelial cells was found, accompanied by a decreased binding of chemokines and L-selectin. Thus, modulation of HS in the glomerular endothelial glycocalyx significantly reduced the inflammatory response in antiglomerular basement membrane nephritis.