Rops Angelique L, van den Hoven Mabel J, Bakker Marinka A, Lensen Joost F, Wijnhoven Tessa J, van den Heuvel Lambert P, van Kuppevelt Toin H, van der Vlag Johan, Berden Jo H
Nephrology Research Laboratory, Division of Nephrology, Department of Matrix Biochemistry, Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen Medical Centre, Geert Grooteplein 26-28, 6525 GA Nijmegen, The Netherlands.
Nephrol Dial Transplant. 2007 Jul;22(7):1891-902. doi: 10.1093/ndt/gfm194. Epub 2007 Jun 5.
Recently, we identified specific N- and 6-O-sulphated heparan sulphate (HS) domains on activated glomerular endothelial cells. In this study, we evaluated in lupus nephritis the expression of different HS domains on glomerular endothelium and in the glomerular basement membrane (GBM).
The expression of specific glomerular HS domains and the presence of immunoglobulins (Ig) were determined by immunofluorescence staining of kidney sections of patients with nephritis due to systemic lupus erythematosus (SLE) and MRL/lpr lupus mice. The expression/presence of glomerular HS domains and Ig was also evaluated after eluting Ig from renal sections of lupus mice using two elution methods, and in renal sections of lupus mice treated with heparinoids.
Both MRL/lpr mice and patients with lupus nephritis showed a decreased expression of HS in the GBM. The expression of N- and 6-O-sulphated HS domains on glomerular endothelium was decreased in MRL/lpr mice, but increased in SLE patients. MRL/lpr mice had more extensive glomerular Ig deposits than SLE patients. After elution of Ig, the glomerular endothelial expression of N- and 6-O-sulphated HS domains in MRL/lpr mice was recovered and even increased above normal levels, while the expression of HS in the GBM was restored to normal levels. Treatment with heparinoids prevented Ig deposition and preserved the expression of glomerular HS domains at normal levels in lupus mice.
The expression of specific HS domains on glomerular endothelium and in the GBM is changed during lupus nephritis due to masking by Ig deposits and induction of inflammatory N- and 6-O-sulphated HS domains.
最近,我们在活化的肾小球内皮细胞上鉴定出了特定的N - 和6 - O - 硫酸化硫酸乙酰肝素(HS)结构域。在本研究中,我们评估了狼疮性肾炎中肾小球内皮和肾小球基底膜(GBM)上不同HS结构域的表达情况。
通过对系统性红斑狼疮(SLE)肾炎患者及MRL/lpr狼疮小鼠肾脏切片进行免疫荧光染色,来确定特定肾小球HS结构域的表达以及免疫球蛋白(Ig)的存在情况。还使用两种洗脱方法从狼疮小鼠的肾脏切片中洗脱Ig后,以及在使用类肝素处理的狼疮小鼠肾脏切片中,评估肾小球HS结构域和Ig的表达/存在情况。
MRL/lpr小鼠和狼疮性肾炎患者的GBM中HS表达均降低。MRL/lpr小鼠肾小球内皮上N - 和6 - O - 硫酸化HS结构域的表达降低,但SLE患者中该表达增加。MRL/lpr小鼠的肾小球Ig沉积比SLE患者更广泛。洗脱Ig后,MRL/lpr小鼠肾小球内皮上N - 和6 - O - 硫酸化HS结构域的表达得以恢复,甚至高于正常水平,而GBM中HS的表达恢复到正常水平。用类肝素治疗可防止Ig沉积,并使狼疮小鼠肾小球HS结构域的表达维持在正常水平。
在狼疮性肾炎期间,由于Ig沉积的掩盖以及炎症性N - 和6 - O - 硫酸化HS结构域的诱导,肾小球内皮和GBM上特定HS结构域的表达发生了变化。