Link M P, Stewart S J, Warnke R A, Levy R
J Clin Invest. 1985 Jul;76(1):248-53. doi: 10.1172/JCI111954.
We have examined the expression of the Leu-4 (T3) antigen on the cell surface and in the cytoplasm of blast cells from 23 patients with T cell acute lymphoblastic leukemia and T cell lymphoblastic lymphoma. In the majority of cases (17), the Leu-4 antigen was absent from the cell surface; however, in 16 of these 17 cases, blast cells demonstrated cytoplasmic expression of Leu-4. This discordance between surface and cytoplasmic expression of Leu-4 was also found in thymocytes and appeared to be restricted to Leu-4, in that tests of other T cell antigens rarely revealed discordance between surface and cytoplasmic expression. To study further the cytoplasmic determinant identified by anti-Leu-4 in malignant T lymphoblasts, immunoprecipitation studies were performed that utilized biosynthetic labeling of established T cell lines derived from T lymphoblastic malignancies. By one-dimensional sodium dodecyl sulfate-polyacrylamide gel electrophoresis, identical Leu-4 polypeptide families were immunoprecipitated from surface Leu-4+ and surface Leu-4-/cytoplasmic Leu-4+ cell lines. Because T lymphoblastic malignancies represent proliferations of immature T cells, and because the cases studied demonstrated surface phenotypes corresponding to all of the proposed stages of T cell ontogeny, it appears that cytoplasmic expression of Leu-4 occurs early in T cell development. The reason for the failure of these immature T cells to transport the Leu-4 molecule to their surface remains to be elucidated.
我们检测了23例T细胞急性淋巴细胞白血病和T细胞淋巴母细胞淋巴瘤患者原始细胞的细胞表面及细胞质中Leu-4(T3)抗原的表达情况。在大多数病例(17例)中,细胞表面不存在Leu-4抗原;然而,在这17例中的16例中,原始细胞显示出Leu-4的细胞质表达。Leu-4在表面和细胞质表达之间的这种不一致性也在胸腺细胞中被发现,并且似乎仅限于Leu-4,因为对其他T细胞抗原的检测很少揭示表面和细胞质表达之间的不一致。为了进一步研究恶性T淋巴母细胞中抗Leu-4识别的细胞质决定簇,进行了免疫沉淀研究,该研究利用了源自T淋巴母细胞恶性肿瘤的已建立T细胞系的生物合成标记。通过一维十二烷基硫酸钠-聚丙烯酰胺凝胶电泳,从表面Leu-4+和表面Leu-4-/细胞质Leu-4+细胞系中免疫沉淀出相同的Leu-4多肽家族。由于T淋巴母细胞恶性肿瘤代表未成熟T细胞的增殖,并且由于所研究的病例显示出与T细胞个体发育的所有提议阶段相对应的表面表型,因此似乎Leu-4的细胞质表达在T细胞发育早期就出现了。这些未成熟T细胞未能将Leu-4分子转运到其表面的原因仍有待阐明。