Department of Nephrology (480), Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA, Nijmegen, The Netherlands.
Adv Exp Med Biol. 2020;1221:647-667. doi: 10.1007/978-3-030-34521-1_26.
The primary filtration of blood occurs in the glomerulus in the kidney. Destruction of any of the layers of the glomerular filtration barrier might result in proteinuric disease. The glomerular endothelial cells and especially its covering layer, the glycocalyx, play a pivotal role in development of albuminuria. One of the main sulfated glycosaminoglycans in the glomerular endothelial glycocalyx is heparan sulfate. The endoglycosidase heparanase degrades heparan sulfate, thereby affecting glomerular barrier function, immune reactivity and inflammation. Increased expression of glomerular heparanase correlates with loss of glomerular heparan sulfate in many glomerular diseases. Most importantly, heparanase knockout in mice prevented the development of albuminuria after induction of experimental diabetic nephropathy and experimental glomerulonephritis. Therefore, heparanase could serve as a pharmacological target for glomerular diseases. Several factors that regulate heparanase expression and activity have been identified and compounds aiming to inhibit heparanase activity are currently explored.
血液的主要过滤发生在肾脏的肾小球中。肾小球滤过屏障的任何一层被破坏都可能导致蛋白尿疾病。肾小球内皮细胞及其覆盖层——糖萼,在白蛋白尿的发生发展中起着关键作用。糖萼中主要的硫酸化糖胺聚糖之一是肝素硫酸盐。内切糖苷酶肝素酶可降解肝素硫酸盐,从而影响肾小球屏障功能、免疫反应和炎症。在许多肾小球疾病中,肾小球肝素酶的表达增加与肾小球肝素硫酸盐的丢失相关。最重要的是,在诱导实验性糖尿病肾病和实验性肾小球肾炎后,敲除小鼠的肾小球肝素酶可防止白蛋白尿的发生。因此,肝素酶可以作为肾小球疾病的药理学靶点。已经确定了几种调节肝素酶表达和活性的因素,目前正在探索旨在抑制肝素酶活性的化合物。