Servettaz Amélie, Guilpain Philippe, Camoin Luc, Mayeux Patrick, Broussard Cédric, Tamby Mathieu C, Tamas Nicolas, Kaveri Srini V, Guillevin Loïc, Mouthon Luc
Faculté de Médecine, UPRES-EA 4058, Université Paris Descartes, Paris, France.
Proteomics. 2008 Mar;8(5):1000-8. doi: 10.1002/pmic.200700794.
In order to identify target antigens of anti-endothelial cell (anti-EC) antibodies (AECA) in healthy individuals, we have used a proteomic approach combining 2-DE and immunoblotting. Whole cell protein extracts obtained from human umbilical vein EC (HUVEC) cultures were used as a source of antigens. Serum IgG from 12 healthy blood donors were tested at a concentration of 200 microg/mL. Targeted spots were identified by MS. The HUVEC proteome was composed of 884 protein spots. Among these, 61 +/- 25.8 (mean +/- SD) spots were recognized by serum IgG from healthy individuals, with marked differences from one individual to another. Among these spots, 11 were recognized by serum IgG from all healthy individuals tested. These spots corresponded to six different proteins with several spots corresponding to different isoforms of the same protein. Target antigens were: cytoskeletal proteins (beta-actin, alpha-tubulin, and vimentin); glycolytic enzymes (glucose-3-phosphate-deshydrogenase and alpha-enolase); and prolyl-4-hydroxylase beta subunit, a member of the disulfide isomerase family. This study shows that the repertoire of IgG AECA is heterogeneous among healthy individuals. IgG from all of the healthy individuals tested recognized a restricted set of highly conserved ubiquitous proteins playing key roles in cell biology and maintenance of homeostasis.
为了鉴定健康个体中抗内皮细胞(anti-EC)抗体(AECA)的靶抗原,我们采用了一种结合二维电泳(2-DE)和免疫印迹的蛋白质组学方法。从人脐静脉内皮细胞(HUVEC)培养物中获得的全细胞蛋白提取物用作抗原来源。对12名健康献血者的血清IgG以200μg/mL的浓度进行检测。通过质谱(MS)鉴定靶向斑点。HUVEC蛋白质组由884个蛋白斑点组成。其中,61±25.8(平均值±标准差)个斑点被健康个体的血清IgG识别,个体之间存在显著差异。在这些斑点中,11个被所有检测的健康个体的血清IgG识别。这些斑点对应于六种不同的蛋白质,有几个斑点对应于同一种蛋白质的不同异构体。靶抗原为:细胞骨架蛋白(β-肌动蛋白、α-微管蛋白和波形蛋白);糖酵解酶(葡萄糖-3-磷酸脱氢酶和α-烯醇化酶);以及脯氨酰-4-羟化酶β亚基,它是二硫键异构酶家族的成员。这项研究表明,健康个体中IgG AECA的组成是异质性的。所有检测的健康个体的IgG都识别一组有限的高度保守的普遍存在的蛋白质,这些蛋白质在细胞生物学和内环境稳态维持中起关键作用。