Secretory leukemic B cells express T cell markers in vitro. A phenomenon suppressed by TPA.

A P Efremidis, H S Haubenstock, N M Papadopoulos, J F Holland, J G Bekesi
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Abstract

Immunological and biochemical markers of leukemia/lymphoma cells have provided valuable insight into hematopoietic malignancy and normal differentiation. The general assumption is that as early lymphoid cells become committed towards terminal differentiation they lose their capacity for bimodal differentiation and cells become restricted to B or T cell development and function. We have observed that phenotypically "late" leukemic B cells close to secretory stage can spontaneously express mature T cell antigens (T11, T4 and T8) after culture in vitro. In further studies of these cells, it was found that the biochemical marker lactate Dehydrogenase (LD) follows the intermediate pattern expressed by thymocytes rather than that of typical B cells. The expression of T cell antigens can be blocked by incubating these cells with the phorbol ester TPA (12-0-tetradecanoyl phorbol 13 acetate) which promotes unidirectional B cell maturation to plasmacytoid cells in a way that mimics normal B cell differentiation. These observations indicate that presecretory malignant B cells are still programmed to express T cell biochemical and antigenic markers and this expression can be influenced by environmental conditions in vitro.

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分泌性白血病B细胞在体外表达T细胞标记物。TPA抑制了这一现象。
白血病/淋巴瘤细胞的免疫学和生化标志物为造血系统的恶性和正常分化提供了有价值的见解。一般的假设是,随着早期淋巴样细胞走向终末分化,它们失去了双峰分化的能力,细胞的发育和功能受到B或T细胞的限制。我们观察到表型上接近分泌期的“晚期”白血病B细胞在体外培养后可以自发表达成熟的T细胞抗原(T11、T4和T8)。在对这些细胞的进一步研究中,发现生化标志物乳酸脱氢酶(LD)遵循胸腺细胞而不是典型B细胞表达的中间模式。T细胞抗原的表达可以通过将这些细胞与phorbol酯TPA(12-0-十四烷醇phorbol 13醋酸酯)孵育来阻断,TPA以一种模仿正常B细胞分化的方式促进B细胞单向成熟为浆细胞样细胞。这些观察结果表明,分泌前恶性B细胞仍然被编程表达T细胞生化和抗原标记物,这种表达可受体外环境条件的影响。
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