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自我更新的造血干细胞是人类慢性淋巴细胞白血病发病机制中的主要靶点。

Self-renewing hematopoietic stem cell is the primary target in pathogenesis of human chronic lymphocytic leukemia.

机构信息

Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka 812-8582, Japan.

出版信息

Cancer Cell. 2011 Aug 16;20(2):246-59. doi: 10.1016/j.ccr.2011.06.029.

Abstract

We report here that in chronic lymphocytic leukemia (CLL), the propensity to generate clonal B cells has been acquired already at the hematopoietic stem cell (HSC) stage. HSCs purified from patients with CLL displayed lymphoid-lineage gene priming and produced a high number of polyclonal B cell progenitors. Strikingly, their maturation into B cells was restricted always to mono- or oligo-clones with CLL-like phenotype in xenogeneic recipients. These B cell clones were independent of the original CLL clones because they had their own immunoglobulin VDJ genes. Furthermore, they used preferentially VH genes frequently used in human CLL, presumably reflecting the role of B cell receptor signaling in clonal selection. These data suggest that HSCs can be involved in leukemogenesis even in mature lymphoid tumors.

摘要

我们在此报告,在慢性淋巴细胞白血病(CLL)中,产生克隆 B 细胞的倾向在造血干细胞(HSC)阶段就已经获得。从 CLL 患者中纯化的 HSCs 显示出淋巴样谱系基因的启动,并且产生了大量的多克隆 B 细胞前体。引人注目的是,在异种受体中,它们的成熟总是局限于具有 CLL 样表型的单克隆或寡克隆。这些 B 细胞克隆与原始 CLL 克隆无关,因为它们具有自己的免疫球蛋白 VDJ 基因。此外,它们优先使用在人类 CLL 中经常使用的 VH 基因,这可能反映了 B 细胞受体信号在克隆选择中的作用。这些数据表明,HSCs 甚至可以参与成熟淋巴细胞肿瘤的白血病发生。

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