Nakagawa Y, Abram V, Parks J H, Lau H S, Kawooya J K, Coe F L
J Clin Invest. 1985 Oct;76(4):1455-62. doi: 10.1172/JCI112124.
One reason that some people are prone to calcium oxalate nephrolithiasis is that they produce urine that is subnormal in its ability to inhibit the growth of calcium oxalate crystals. We have identified in human urine a glycoprotein (GCI) that inhibits calcium oxalate crystal growth strongly, and at low concentrations (10(-7) M); in this study, we have isolated GCI molecules from the urine of normal people and patients with calcium oxalate stones. GCI from stone formers is abnormal in three ways: it contains no detectable gamma-carboxyglutamic acid (Gla), whereas normal GCI contains 2-3 residues of Gla per mole; about half of the GCI in urine of patients inhibits crystal growth 4-20 times less than normal GCI as judged by its performance in a kinetic growth assay, in vitro; at the air-water interface, patient GCI has a film collapse pressure approximately half of normal. GCI molecules from the urine of patients with calcium oxalate nephrolithiasis are intrinsically abnormal, and these abnormalities could play a role in the genesis of stones.
一些人易患草酸钙肾结石的一个原因是他们产生的尿液抑制草酸钙晶体生长的能力低于正常水平。我们在人尿中鉴定出一种糖蛋白(GCI),它能在低浓度(10^(-7) M)时强烈抑制草酸钙晶体生长;在本研究中,我们从正常人及草酸钙结石患者的尿液中分离出了GCI分子。结石患者的GCI在三个方面存在异常:它不含可检测到的γ-羧基谷氨酸(Gla),而正常GCI每摩尔含有2 - 3个Gla残基;通过体外动力学生长试验判断,患者尿液中约一半的GCI抑制晶体生长的能力比正常GCI低4 - 20倍;在气-水界面,患者的GCI具有的膜塌陷压力约为正常的一半。草酸钙肾结石患者尿液中的GCI分子本质上是异常的,这些异常可能在结石的形成过程中起作用。