Manukyan Gayane, Mikulkova Zuzana, Turcsanyi Peter, Savara Jakub, Trajerová Markéta, Kubova Zuzana, Papajik Tomas, Kriegova Eva
Department of Immunology, Faculty of Medicine and Dentistry, Palacký University and University Hospital, 77900 Olomouc, Czech Republic.
Laboratory of Molecular and Cellular Immunology, Institute of Molecular Biology NAS RA, Yerevan 0014, Armenia.
Cancers (Basel). 2021 Sep 30;13(19):4922. doi: 10.3390/cancers13194922.
Chronic lymphocytic leukaemia (CLL) is a genetically, morphologically and phenotypically heterogeneous chronic disease with clinical variability between patients. Whether the significant heterogeneity of cell size within the CLL population contributes to the heterogeneous features of this disease has not been investigated. The present study aimed to characterise the phenotypic and functional properties of two subpopulations of typical CLL cells that differ in cell size: small (s-CLL) and large (l-CLL) CLL cells delineated by forward scatter cytometry. The s-CLL cells were characterised by the CD5CXCR4 phenotype, while the l-CLL cells were characterised by the CD5CXCR4 phenotype and indicated a higher expression of CXCR3, CD20, CD38 and HLA-DR. The l-CLL cells displayed higher migration activity towards CXCL12, a tendency towards a higher proliferation rate and an increased capacity to produce IgM in the presence of CpG compared with s-CLL cells. When stimulated with CpG and CXCL12, l-CLL cells were characterised by a higher polarisation phenotype and motility than s-CLL cells. Our study revealed that the differences in CLL cell size reflected their activation status, polarisation and migratory abilities. Our data provide evidence of the importance of cell-size heterogeneity within a CLL pool and the dynamics of cell-size changes for disease pathogenesis, thus deserving further investigation.
慢性淋巴细胞白血病(CLL)是一种在遗传、形态和表型上具有异质性的慢性疾病,患者之间存在临床变异性。CLL群体中细胞大小的显著异质性是否导致了该疾病的异质性特征尚未得到研究。本研究旨在表征两种典型CLL细胞亚群的表型和功能特性,这两种亚群在细胞大小上存在差异:通过前向散射细胞术划分出的小(s-CLL)和大(l-CLL)CLL细胞。s-CLL细胞以CD5CXCR4表型为特征,而l-CLL细胞以CD5CXCR4表型为特征,并显示出CXCR3、CD20、CD38和HLA-DR的更高表达。与s-CLL细胞相比,l-CLL细胞对CXCL12表现出更高的迁移活性,具有更高增殖率的趋势,并且在存在CpG的情况下产生IgM的能力增强。当用CpG和CXCL12刺激时,l-CLL细胞比s-CLL细胞表现出更高的极化表型和运动性。我们的研究表明,CLL细胞大小的差异反映了它们的激活状态、极化和迁移能力。我们的数据证明了CLL库中细胞大小异质性以及细胞大小变化动态对疾病发病机制的重要性,因此值得进一步研究。