Li Y F, Kawashima H, Watanabe N, Miyasaka M
Department of Bioregulation, Biomedical Research Center, Osaka University Medical School, Suita, Japan.
FEBS Lett. 1999 Feb 12;444(2-3):201-5. doi: 10.1016/s0014-5793(99)00046-0.
Ligands for the leukocyte adhesion molecule L-selectin are expressed not only in lymph node high endothelial venules (HEV) but also in the renal distal tubuli. Here we report that L-selectin-reactive molecules in the kidney are chondroitin sulfate and heparan sulfate proteoglycans of 500-1000 kDa, unlike those in HEV bearing sialyl Lewis X-like carbohydrates. Binding of L-selectin to these molecules was mediated by the lectin domain of L-selectin and required divalent cations. Binding was inhibited by chondroitinase and/or heparitinase but not sialidase. Thus, L-selectin can recognize chondroitin sulfate and heparan sulfate glycosaminoglycans structurally distinct from sialyl Lewis X-like carbohydrates.
白细胞黏附分子L-选择素的配体不仅在淋巴结高内皮微静脉(HEV)中表达,也在肾远曲小管中表达。在此我们报告,肾脏中与L-选择素反应的分子是500 - 1000 kDa的硫酸软骨素和硫酸乙酰肝素蛋白聚糖,这与带有唾液酸化路易斯X样碳水化合物的HEV中的分子不同。L-选择素与这些分子的结合由L-选择素的凝集素结构域介导,并且需要二价阳离子。结合被硫酸软骨素酶和/或肝素酶抑制,但不被唾液酸酶抑制。因此,L-选择素能够识别结构上不同于唾液酸化路易斯X样碳水化合物的硫酸软骨素和硫酸乙酰肝素糖胺聚糖。