Park S H, Bae Y M, Kwon H J, Kim T J, Kim J, Lee S J, Lee S K
Department of Pathology, Seoul National University College of Medicine, Korea.
J Exp Med. 1993 Oct 1;178(4):1447-51. doi: 10.1084/jem.178.4.1447.
Expression of a novel thymocyte differentiation antigen, JL1, defined by a monoclonal antibody (mAb) developed against human thymocytes showed a specificity for stage II double positive (CD4+CD8+) human cortical thymocytes. This antigen was not expressed at detectable levels on medullary thymocytes, mature peripheral leukocytes, bone marrow cells or on other types of tissues elsewhere in the human body. Immunohistologic analysis revealed that JL1 had a clear pattern of distribution on cortical thymocytes. Immunoprecipitation of 125I-labeled cell lysates from human thymocytes and Molt-4 leukemic cell line with anti-JL1 mAb yielded a 120-130-kD single chain glycoprotein. When immunoprecipitation of cell lysate was done after endoglycosidase F treatment, JL1 antigen was still detected by antibody but the band showed a reduction in apparent molecular mass of approximately 5 kD. This suggests that, although JL1 molecule contains carbohydrate group, this does not form a critical part of the antigenic determinant for anti-JL1 antibody. JL1 antigen appears to be the first double positive, stage-specific differentiation antigen of human thymocyte reported so far. This antigen would be a useful marker for lymphoblastic malignancy of stage II thymocyte origin and it may be involved in the thymocyte education process.
一种新型胸腺细胞分化抗原JL1的表达,该抗原由针对人胸腺细胞产生的单克隆抗体(mAb)所定义,显示出对II期双阳性(CD4+CD8+)人皮质胸腺细胞具有特异性。在髓质胸腺细胞、成熟外周白细胞、骨髓细胞或人体其他部位的其他类型组织上,未检测到该抗原的表达。免疫组织学分析显示,JL1在皮质胸腺细胞上具有清晰的分布模式。用抗JL1 mAb对人胸腺细胞和Molt-4白血病细胞系的125I标记细胞裂解物进行免疫沉淀,产生了一条120 - 130 kD的单链糖蛋白。在内切糖苷酶F处理后对细胞裂解物进行免疫沉淀时,抗体仍能检测到JL1抗原,但条带的表观分子量降低了约5 kD。这表明,尽管JL1分子含有碳水化合物基团,但这并非抗JL1抗体抗原决定簇的关键部分。JL1抗原似乎是迄今为止报道的首个双阳性、阶段特异性的人胸腺细胞分化抗原。该抗原将是II期胸腺细胞来源的淋巴细胞恶性肿瘤的有用标志物,并且可能参与胸腺细胞的发育过程。