Nakayama Kenji, Natori Yumiko, Sato Toshinobu, Kimura Tomoyoshi, Sugiura Akira, Sato Hiroshi, Saito Takao, Ito Sadayoshi, Natori Yasuhiro
Research Institute, International Medical Center of Japan, Tokyo, Japan.
J Lab Clin Med. 2004 Feb;143(2):106-14. doi: 10.1016/j.lab.2003.10.012.
Sulfated portions of glycosaminoglycan (GAG) side chains in heparan sulfate proteoglycan (HSPG) are thought to play an important role in charge-dependent selectivity of glomerular filtration against plasma proteins. Heparan sulfate N-acetylglucosamine N-deacetylase/adenosine 3'-phosphate 5'-phosphosulfate: unsubstituted glucosamine N-sulfotransferase (NDST) is the key enzyme regulating sulfation of GAG chains. In this study we investigated transcriptional expression of NDST-1, 1 of 4 isozymes of NDST, in glomeruli of rats with puromycin aminonucleoside (PAN) nephrosis. Nephrosis was induced in rats with a single intraperitoneal injection of 150 mg/kg PAN. On days 10 and 35, expression of NDST-1 messenger RNA (mRNA) in glomeruli was analyzed with the use of Northern-blot analysis. Immunohistochemical studies were also performed with the use of monoclonal antibodies that react specifically with the N-sulfated portion of the GAG chain of HSPG and agrin, a major core protein of HSPG in glomerular basement membrane (GBM). In addition, we studied the expression of NDST-1 mRNA in cultured glomerular epithelial cells (GECs) and glomerular mesangial cells in the presence of PAN. On day 10, when significant proteinuria developed, the ratios of glomerular expression of NDST-1 mRNA against glyceraldehyde-phosphate dehydrogenase mRNA in PAN-treated rats were decreased to 48% +/- 6% of those in controls (P<.05). Immunohistochemical studies revealed that staining for N-sulfated GAG chains of HSPG on GBM was markedly reduced on day 10 in PAN-treated rats but that staining for agrin was unchanged. In contrast, on day 35, when PAN-treated rats recovered from proteinuria, we noted no differences in glomerular expression of NDST-1 mRNA and staining intensity for N-sulfated GAG chains on GBM between PAN-treated rats and controls. Incubation of GECs for 24 hours in the presence of 50 ng/mL PAN resulted in the reduction of the expression of NDST-1 mRNA (67% +/- 12% of those in controls, P<.05). In summary, we found alteration of the expression of NDST-1 mRNA, accompanying a loss of N-sulfated GAG chains of HSPG on GBM without changes in the core protein agrin, in the course of PAN nephrosis. These data suggest an important role for this enzyme in heparan sulfate assembly in GBM and GEC and in the pathogenesis of proteinuria in PAN nephrosis.
硫酸乙酰肝素蛋白聚糖(HSPG)中糖胺聚糖(GAG)侧链的硫酸化部分被认为在肾小球滤过对血浆蛋白的电荷依赖性选择性中起重要作用。硫酸乙酰肝素N - 乙酰葡糖胺N - 脱乙酰酶/腺苷3'-磷酸5'-磷酸硫酸酯:未取代葡糖胺N - 磺基转移酶(NDST)是调节GAG链硫酸化的关键酶。在本研究中,我们调查了嘌呤霉素氨基核苷(PAN)肾病大鼠肾小球中NDST - 1(NDST的4种同工酶之一)的转录表达。通过单次腹腔注射150 mg/kg PAN诱导大鼠肾病。在第10天和第35天,使用Northern印迹分析来分析肾小球中NDST - 1信使核糖核酸(mRNA)的表达。还使用与HSPG的GAG链的N - 硫酸化部分和集聚蛋白(肾小球基底膜(GBM)中HSPG的主要核心蛋白)特异性反应的单克隆抗体进行免疫组织化学研究。此外,我们研究了在PAN存在下培养的肾小球上皮细胞(GECs)和肾小球系膜细胞中NDST - 1 mRNA的表达。在第10天,当出现明显蛋白尿时,PAN处理大鼠中NDST - 1 mRNA相对于甘油醛 - 3 - 磷酸脱氢酶mRNA的肾小球表达比率降至对照组的48%±6%(P<0.05)。免疫组织化学研究显示,在PAN处理的大鼠中,第10天时GBM上HSPG N - 硫酸化GAG链的染色明显减少,但集聚蛋白的染色未改变。相反,在第35天,当PAN处理的大鼠从蛋白尿中恢复时,我们注意到PAN处理大鼠与对照组之间肾小球中NDST - 1 mRNA的表达以及GBM上N - 硫酸化GAG链的染色强度没有差异。在50 ng/mL PAN存在下将GECs孵育24小时导致NDST - 1 mRNA的表达降低(为对照组的67%±12%,P<0.05)。总之,我们发现在PAN肾病过程中,NDST - 1 mRNA的表达发生改变,同时GBM上HSPG的N - 硫酸化GAG链丢失,而核心蛋白集聚蛋白没有变化。这些数据表明该酶在GBM和GEC中的硫酸乙酰肝素组装以及PAN肾病蛋白尿的发病机制中起重要作用。