Parzy D, Fusai T, Pouvelle B, Torrentino M, Eustacchio F, Lépolard C, Scherf A, Gysin J
Unité de parasitologie IMTSSA, Jardin du Pharo, Boulevard Charles Livon, Marseille, France.
Microbes Infect. 2000 Jun;2(7):779-88. doi: 10.1016/s1286-4579(00)90357-5.
The proteoglycan thrombomodulin has been shown to be involved, via its chondroitin-sulfate moiety, in the cytoadhesion of chondroitin-4-sulfate-binding-Plasmodium falciparum-infected erythrocytes to endothelial cells and syncytiotrophoblasts. We cloned and expressed in CHO and COS-7 cells a gene encoding soluble human recombinant thrombomodulin, with a chondroitin-4-sulfate moiety. This system is complementary to the in vitro cell models currently used to study the chondroitin-4-sulfate-binding phenotype. It also provides a means of overcoming the lack of specificity observed in interactions of infected erythrocytes with modified chondroitin-4-sulfate. This thrombomodulin displayed normal activity in coagulation, indicating that it was in a functional conformation. The recombinant protein, whether produced in CHO or COS-7 cells, inhibited cytoadhesion to Saimiri brain microvascular endothelial cells 1D infected with Palo-Alto(FUP)1 parasites selected for chondroitin-4-sulfate receptor preference. Thus, the recombinant protein was produced with a chondroitin-sulfate moiety, identified as a chondroitin-4-sulfate, in both cell types. In both cases, the recombinant protein bound to the chondroitin-4-sulfate phenotype, but not to CD36- and ICAM-1-binding parasites. The chondroitin-4-sulfate was 36 kDa in size for CHO and 17.5 kDa for COS-7 cells. There was, however, no difference in the capacities of the recombinant proteins produced by the two cell types to inhibit the cytoadhesion of infected erythrocytes. Thrombomodulin immobilized on plastic or coupled to Dynabeads was used to purify specifically the infected erythrocytes that bind to chondroitin-4-sulfate. These infected erythrocytes were cultured to establish parasite lines of this phenotype. We then showed that the thrombomodulin, labeled with FITC, could be used to detect this phenotype in blood samples. Finally, the direct binding of infected erythrocytes to immobilized thrombomodulin was used to screen for anti-chondroitin-4-sulfate-binding antibodies.
蛋白聚糖血栓调节蛋白已被证明通过其硫酸软骨素部分参与硫酸软骨素-4结合的恶性疟原虫感染红细胞与内皮细胞及合体滋养层细胞的细胞黏附。我们在CHO和COS-7细胞中克隆并表达了一个编码具有硫酸软骨素-4部分的可溶性人重组血栓调节蛋白的基因。该系统是对目前用于研究硫酸软骨素-4结合表型的体外细胞模型的补充。它还提供了一种方法来克服在感染红细胞与修饰的硫酸软骨素-4相互作用中观察到的特异性缺乏。这种血栓调节蛋白在凝血中表现出正常活性,表明它处于功能构象。无论在CHO细胞还是COS-7细胞中产生,重组蛋白都能抑制与因硫酸软骨素-4受体偏好而选择的帕洛阿尔托(FUP)1寄生虫感染的松鼠猴脑微血管内皮细胞1D的细胞黏附。因此,在两种细胞类型中产生的重组蛋白都带有被鉴定为硫酸软骨素-4的硫酸软骨素部分。在这两种情况下,重组蛋白都与硫酸软骨素-4表型结合,但不与CD36和ICAM-1结合的寄生虫结合。对于CHO细胞,硫酸软骨素-4的大小为36 kDa,对于COS-7细胞为17.5 kDa。然而,两种细胞类型产生的重组蛋白抑制感染红细胞细胞黏附的能力没有差异。固定在塑料上或偶联到磁珠上的血栓调节蛋白用于特异性纯化与硫酸软骨素-4结合的感染红细胞。培养这些感染红细胞以建立这种表型的寄生虫株系。然后我们表明,用异硫氰酸荧光素标记的血栓调节蛋白可用于检测血样中的这种表型。最后,利用感染红细胞与固定化血栓调节蛋白的直接结合来筛选抗硫酸软骨素-4结合抗体。