一种新的人骨髓单核细胞样细胞系P39/Tsugane,来源于骨髓增生异常综合征后的明显白血病。

Gan Pub Date : 1984-12-01
M Nagai, S Seki, T Kitahara, T Abe, K Minato, S Watanabe, M Shimoyama
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引用次数: 0

摘要

一种新的人类培养细胞系P39/Tsugane是从一名69岁男性骨髓增生异常综合征(MDS)后明显白血病的外周血白血病细胞中建立的。P39/Tsugane细胞的特征是胚状外观,存在naff敏感的α -萘基丁酸酯酶活性,Fc γ受体,c3受体,吞噬致敏红细胞的能力,以及与OKT4, My4, VIMD5, MCS-2和My7等单克隆抗体的反应性。这些数据表明P39/Tsugane细胞具有髓单核细胞样性质。P39/Tsugane具有次二倍体染色体结构,获得一致的标记6q+,存在不一致的标记9q+和rcp(14;16),随机和非随机丢失常染色体:根据已报道的MDS细胞遗传学谱,本细胞系的代表性核型为45,XY,+del(6)(q15),9q+, t(14;16)-(q24;q21),-16,-17。P39/Tsugane细胞可腹腔移植到裸鼠体内,产生腹腔肿瘤和出血性腹水。这些结果表明P39/Tsugane是MDS后从显性白血病中获得的第一个培养的髓单核细胞样细胞系。因此,P39/Tsugane细胞可用于白血病细胞分化、MDS发病机制及体内外实验化疗的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel human myelomonocytoid cell line, P39/Tsugane, derived from overt leukemia following myelodysplastic syndrome.

A novel human cultured cell line, P39/Tsugane, was established from leukemic cells in the peripheral blood of a 69-year-old male with overt leukemia following myelodysplastic syndrome (MDS). P39/Tsugane cells were characterized by blastic appearance, presence of NaF-sensitive alpha-naphthyl butylate esterase activity, Fc gamma-receptor, C3-receptor, capacity to phagocytize sensitized erythrocytes, and reactivity with monoclonal antibodies such as OKT4, My4, VIMD5, MCS-2 and My7. These data indicate that P39/Tsugane cells are of myelomonocytoid nature. P39/Tsugane had a hypodiploid chromosome constitution with a gain of a consistent marker, 6q+, the presence of less consistent markers 9q+ and rcp(14;16), and random and non-random losses of autosomes: in accordance with the reported cytogenetic profiles of MDS, a representative karyotype of the present cell line is 45,XY,+del(6)(q15),9q+, t(14;16)-(q24;q21),-16,-17. P39/Tsugane cells were transplantable intraperitoneally into nude mice, and produced abdominal tumors and hemorrhagic ascites. These results indicate that P39/Tsugane is the first cultured cell line of myelomonocytoid nature to be derived from overt leukemia following MDS. Therefore, P39/Tsugane cells should be useful for studies on the differentiation of leukemia cells, the pathogenesis of MDS and in vitro-in vivo experimental chemotherapy.

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