Medical and Molecular Biosciences, University of Technology, Sydney, NSW, Australia.
Int J Lab Hematol. 2010 Dec;32(6 Pt 1):e190-6. doi: 10.1111/j.1751-553X.2010.01222.x.
The use of CD138 to isolate CD138(+) plasma cells (PCs) from plasma cell myeloma (PCM) patients' bone marrow samples has been used extensively in myeloma research. We sought to highlight the problem with this selection process, by demonstrating that a subpopulation of CD138⁻ plasma cells exists which is not included in these analyses.
Retrospective analysis of a patient database was carried out on all PCM patient bone marrow biopsies taken between 4/9/07 and 18/2/09 (n = 218). CD138(+) and CD138⁻ cell populations were separated using flow cytometry cell sorter then analyzed for percentage of cells in S phase using plasma cell labeling index as an indicator of proliferation.
Database results indicated a CD138⁻ PC population in all PCM patient samples which also had a significantly increased (r = 0.53; P < 0.0001) CD45 expression, an indicator or immaturity. Flow cytometric analysis demonstrated the presence of a more immature, higher proliferating CD138⁻ PC population through a significantly (t = 3.26; P < 0.02) higher number of CD138⁻ PCs in S phase compared with the CD138(+) cells.
We have characterised the CD138⁻ PCs as more immature and with a significantly higher proliferative potential. The current trend to ignore this more immature and proliferative subpopulation of malignant PCs may have serious implications when determining gene expression, classifications and drug sensitivity of the malignancy.
从多发性骨髓瘤(PCM)患者的骨髓样本中使用 CD138 分离 CD138(+)浆细胞(PC)已广泛应用于骨髓瘤研究。我们试图通过证明存在未包括在这些分析中的 CD138⁻浆细胞亚群来突出这个选择过程中的问题。
对 2007 年 4 月 9 日至 2009 年 2 月 18 日期间采集的所有 PCM 患者骨髓活检的患者数据库进行回顾性分析(n = 218)。使用流式细胞分选仪分离 CD138(+)和 CD138⁻细胞群,然后通过浆细胞标记指数分析 S 期细胞的百分比来分析增殖。
数据库结果表明,所有 PCM 患者样本中均存在 CD138⁻PC 群,其 CD45 表达也显著增加(r = 0.53;P < 0.0001),这是幼稚的标志。流式细胞术分析表明,存在更幼稚、增殖能力更强的 CD138⁻PC 群,与 CD138(+)细胞相比,S 期的 CD138⁻PC 数量明显更多(t = 3.26;P < 0.02)。
我们已经确定 CD138⁻PC 作为更幼稚和具有更高增殖潜力的细胞。目前忽视这种更幼稚和增殖性恶性 PC 亚群的趋势,可能在确定恶性肿瘤的基因表达、分类和药物敏感性方面产生严重影响。