骨髓增生性疾病患者中涉及CFU-GEMM、BFU-E和CFU-C的克隆性疾病的细胞遗传学证据

H Sugiyama, S Ichiba, Y Okuno, T Takahashi, H Imura, K Nakamura, S Iho, T Hoshino, T Okada, H Furukawa
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引用次数: 0

摘要

我们在体外培养了4例染色体畸变的骨髓增殖性疾病(MPD)患者的多系造血菌落,并在培养第14天对单个cfu - gem、BFU-E和cfu - c衍生菌落进行了细胞遗传学分析。在急性骨髓纤维化患者1中,CFU-GEMM和BFU-E菌落只有47、XX和+C核型。真性红细胞增多症患者2中,CFU-GEMM、BFU-E和CFU-C菌落均显示相同的46、XY、-12、+der(12)t异常核型(1;12)。患者3、4为原发性骨髓纤维化,CFU-GEMM、BFU-E、CFU-C菌落核型分别为46、XY、13q-和46、XX、-6、+der(6)t(1;6)。在这4例患者中,骨髓或循环单核细胞的核型与造血集落相同。这些结果表明MPD的克隆起源在CFU-GEMM水平。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cytogenetic evidence for a clonal disorder involving CFU-GEMM, BFU-E and CFU-C in patients with myeloproliferative disorders.

We grew multilineage hemopoietic colonies in vitro from 4 patients with myeloproliferative disorders (MPD) having chromosomal aberration, and performed cytogenetic analysis of single CFU-GEMM, BFU-E and CFU-C-derived colonies on Day 14 of culture. In Patient 1 with acute myelofibrosis, CFU-GEMM and BFU-E colonies had only a 47, XX, +C karyotype. In Patient 2 with polycythemia vera, CFU-GEMM, BFU-E and CFU-C colonies all showed the same abnormal karyotype of 46, XY, -12, +der(12)t(1;12). Patients 3 and 4 had primary myelofibrosis, and their respective karyotypes were 46, XY, 13q- and 46, XX, -6, +der(6)t(1;6) in CFU-GEMM, BFU-E and CFU-C colonies. In these 4 patients, the karyotype of bone marrow or circulating mononuclear cells was identical to that of hemopoietic colonies. These results indicate a clonal origin of MPD at the level of CFU-GEMM.

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