Endothelial glycocalyx restoration by growth factors in diabetic nephropathy

被引:13
作者
Desideri, Sara [1 ]
Onions, Karen L. [1 ]
Baker, Sian L. [1 ]
Gamez, Monica [1 ]
Hussien, Hesham El Hegni E. [1 ]
Russell, Amy [1 ]
Satchell, Simon C. [1 ]
Foster, Rebecca R. [1 ]
机构
[1] Univ Bristol, Bristol Med Sch, Translat Hlth Sci, Bristol Renal,Bristol Heart Inst, Bristol, Avon, England
关键词
Endothelial glycocalyx; diabetes; diabetic nephropathy; VEGF; VEGFC; VEGFA; VEGF(165)b; angiopoietin-1; vascular permeability; glomerulus; glomerular permeability; GLOMERULAR-BASEMENT-MEMBRANE; HEPARAN-SULFATE; IN-VIVO; CELL GLYCOCALYX; VEGF-A; CARDIOVASCULAR-DISEASE; INCREASED EXPRESSION; CHONDROITIN SULFATE; SPLICE VARIANT; RISK-FACTORS;
D O I
10.3233/BIR-180199
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The endothelial glycocalyx (eGlx) constitutes the first barrier to protein in all blood vessels. This is particularly noteworthy in the renal glomerulus, an ultrafiltration barrier. Leakage of protein, such as albumin, across glomerular capillaries results in albumin in the urine (albuminuria). This is a hall mark of kidney disease and can reflect loss of blood vessel integrity in microvascular beds elsewhere. We discuss evidence demonstrating that targeted damage to the glomerular eGlx results in increased glomerular albumin permeability. EGlx is lost in diabetes and experimental models demonstrate loss from glomerular endothelial cells. Vascular endothelial growth factor (VEGF)A is upregulated in early diabetes, which is associated with albuminuria. Treatment with paracrine growth factors such as VEGFC, VEGF 165 b and angiopoietin-1 can modify VEGFA signalling, rescue albumin permeability and restore glomerular eGlx in models of diabetes. Manipulation of VEGF receptor 2 signalling, or a common eGlx biosynthesis pathway by these growth factors, may protect and restore the eGlx layer. This would help to direct future therapeutics in diabetic nephropathy.
引用
收藏
页码:163 / 179
页数:17
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