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B 细胞慢性淋巴细胞白血病细胞在细胞周期的不同阶段显示出膜蛋白表达的特定变化。

B-cell chronic lymphocytic leukaemia cells show specific changes in membrane protein expression during different stages of cell cycle.

作者信息

Bennett Fiona, Rawstron Andy, Plummer Marieth, de Tute Ruth, Moreton Paul, Jack Andrew, Hillmen Peter

机构信息

Haematological Malignancy Diagnostic Service, Leeds Teaching Hospitals, Leeds, UK.

出版信息

Br J Haematol. 2007 Nov;139(4):600-4. doi: 10.1111/j.1365-2141.2007.06790.x.

Abstract

The proliferating component in chronic lymphocytic leukaemia (CLL) is usually small (<1%) and restricted to a specific micro-environmental niche. To characterize the proliferating component, CLL cells from bone marrow or lymph nodes of 23 patients were assessed for expression of up to 66 surface antigens in combination with nuclear Ki-67/MCM6. Ki-67 expression was associated with step-wise increases in CD23/CD95/CD86/CD39/CD27 and decreases in CD24/CD69/CXCR4/CXCR5. Ki-67+ cells showed increased CD38 expression, but with considerable inter-patient variability: in some cases Ki-67 expression was only detectable in CD38- CLL cells. The results suggest continuous re-entry into the cell cycle as no distinct stem cell pool was detectable.

摘要

慢性淋巴细胞白血病(CLL)中的增殖成分通常很少(<1%),且局限于特定的微环境龛。为了表征增殖成分,对23例患者骨髓或淋巴结中的CLL细胞进行评估,检测其多达66种表面抗原的表达,并结合核Ki-67/MCM6进行分析。Ki-67表达与CD23/CD95/CD86/CD39/CD27的逐步增加以及CD24/CD69/CXCR4/CXCR5的减少相关。Ki-67+细胞显示CD38表达增加,但患者间存在相当大的变异性:在某些情况下,仅在CD38-的CLL细胞中可检测到Ki-67表达。结果表明细胞持续重新进入细胞周期,因为未检测到明显的干细胞池。

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