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Small and big Hodgkin-Reed-Sternberg cells of Hodgkin lymphoma cell lines L-428 and L-1236 lack consistent differences in gene expression profiles and are capable to reconstitute each other

机译:霍奇金淋巴瘤细胞系L-428和L-1236的大小霍奇金-里德-斯特恩贝格细胞在基因表达谱上缺乏一致的差异并且能够相互重构

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摘要

The hallmark of classical Hodgkin lymphoma (cHL) is the presence of giant, mostly multinucleated Hodgkin-Reed-Sternberg (HRS) cells. Whereas it has recently been shown that giant HRS cells evolve from small Hodgkin cells by incomplete cytokinesis and re-fusion of tethered sister cells, it remains unsolved why this phenomenon particularly takes place in this lymphoma and what the differences between these cell types of variable sizes are. The aim of the present study was to characterize microdissected small and giant HRS cells by gene expression profiling and to assess differences of clonal growth behavior as well as susceptibility toward cytotoxic intervention between these different cell types to provide more insight into their distinct cellular potential. Applying stringent filter criteria, only two differentially expressed genes between small and giant HRS cells, SHFM1 and LDHB, were identified. With looser filter criteria, 13 genes were identified to be differentially overexpressed in small compared to giant HRS cells. These were mainly related to energy metabolism and protein synthesis, further suggesting that small Hodgkin cells resemble the proliferative compartment of cHL. SHFM1, which is known to be involved in the generation of giant cells, was downregulated in giant RS cells at the RNA level. However, reduced mRNA levels of SHFM1, LDHB and HSPA8 did not translate into decreased protein levels in giant HRS cells. In cell culture experiments it was observed that the fraction of small and big HRS cells was adjusted to the basic level several days after enrichment of these populations via cell sorting, indicating that small and big HRS cells can reconstitute the full spectrum of cells usually observed in the culture. However, assessment of clonal growth of HRS cells indicated a significantly reduced potential of big HRS cells to form single cell colonies. Taken together, our findings pinpoint to strong similarities but also some differences between small and big HRS cells.
机译:经典霍奇金淋巴瘤(cHL)的标志是存在巨大的,多核的霍奇金-里德-斯特恩伯格(HRS)细胞。尽管最近发现巨人HRS细胞是通过不完全胞质分裂和拴系姐妹细胞的重新融合而从小的霍奇金细胞进化而来的,但仍未解决为什么这种现象特别发生在该淋巴瘤中以及这些可变大小的细胞类型之间的差异为何仍未解决是。本研究的目的是通过基因表达谱表征显微切割的小型和巨型HRS细胞,并评估这些不同细胞类型之间克隆生长行为的差异以及对细胞毒性干预的敏感性,以进一步了解其独特的细胞潜力。应用严格的筛选标准,在小型和巨型HRS细胞之间只有两个差异表达的基因SHFM1和LDHB被鉴定。使用较宽松的筛选标准,与巨型HRS细胞相比,在小型中鉴定出13个差异表达的基因。这些主要与能量代谢和蛋白质合成有关,进一步表明小的霍奇金细胞类似于cHL的增殖区室。已知参与巨细胞生成的SHFM1在RNA水平上在巨RS细胞中被下调。但是,SHFM1,LDHB和HSPA8的mRNA水平降低并未转化为巨型HRS细胞中的蛋白质水平降低。在细胞培养实验中,观察到在通过细胞分选富集这些种群数天后,小和大HRS细胞的比例被调整到基本水平,这表明小和大HRS细胞可以重构通常在细胞中观察到的整个细胞谱。文化。然而,对HRS细胞的克隆生长的评估表明,大HRS细胞形成单细胞集落的潜力显着降低。综上所述,我们的发现指出了HRS小细胞与大HRS细胞之间的强相似性,但也存在一些差异。

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