Bardin N, George F, Mutin M, Brisson C, Horschowski N, Francés V, Lesaule G, Sampol J
Laboratoire d'Hématologie, Faculté de Pharmacie, Marseille, France.
Tissue Antigens. 1996 Nov;48(5):531-9. doi: 10.1111/j.1399-0039.1996.tb02666.x.
A murine monoclonal antibody (mAb) S-Endo 1 has been produced to detect circulating endothelial cells detached from blood vessels in pathological conditions. We have demonstrated that the associated-antigen (S-Endo 1 Ag) was highly expressed on human vascular structure irrespective of tissue origin or vessel caliber. Its expression was not restricted to endothelium, since it was also detected at low level on smooth muscle cells, stroma cells and follicular dendritic cells. But its absence on hematopoietic cells made S-Endo 1 a helpful reagent to specifically discriminate endothelium from hematopoietic tissues. Biochemical characterization showed that S-Endo 1 recognizes a monomeric structure of approximately 118 kDa on cultured endothelial cells. S-Endo 1 was submitted to the 5th International Workshop (Boston, 1993) and did not cluster in any of the old or new endothelial clusters discussed at the conference, indicating its unique reactivity. Together with the data presented in this paper, this suggested that S-Endo 1 defines a previously undescribed endothelial molecule.
已制备出一种鼠单克隆抗体(mAb)S-Endo 1,用于检测在病理状态下从血管脱离的循环内皮细胞。我们已证明,相关抗原(S-Endo 1 Ag)在人类血管结构上高度表达,与组织来源或血管口径无关。其表达不限于内皮细胞,因为在平滑肌细胞、基质细胞和滤泡树突状细胞上也能检测到低水平表达。但造血细胞上不存在该抗原,这使得S-Endo 1成为一种有助于从造血组织中特异性区分内皮细胞的有用试剂。生化特性表明,S-Endo 1识别培养内皮细胞上约118 kDa的单体结构。S-Endo 1被提交至第五届国际研讨会(1993年,波士顿),在会议讨论的任何旧的或新的内皮细胞簇中均未聚类,表明其具有独特的反应性。结合本文给出的数据,这表明S-Endo 1定义了一种先前未描述的内皮分子。