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首页> 外文期刊>Cartilage >The Oncogene LRF Stimulates Proliferation of Mesenchymal Stem Cells and Inhibits Their Chondrogenic Differentiation
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The Oncogene LRF Stimulates Proliferation of Mesenchymal Stem Cells and Inhibits Their Chondrogenic Differentiation

机译:癌基因LRF刺激间充质干细胞的增殖并抑制其软骨分化

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摘要

Objective. The oncogene leukemia/lymphoma-related factor (LRF) enhances chondrosarcoma proliferation and malignancy. This study aimed to investigate the roles of LRF in chondrogenic differentiation of primary human bone marrow-derived mesenchymal stem cells (BMSCs). Design. LRF was overexpressed in BMSC by lentiviral transduction. Chondrogenic differentiation of BMSC was induced by high-density pellet culture. Western blotting and real-time polymerase chain reaction were used to investigate changes in protein and mRNA levels, respectively, during chondrogenesis. Safranin-O staining, immunohistochemistry, and glycoaminoglycan contents were used to assess cartilage matrix deposition. BMSC proliferation was determined by mitochondrial dehydrogenase activity and cell counting. Cell cycle profiling was performed by flow cytometry. Results. LRF overexpression effectively inhibited protein and mRNA expression of chondrocyte markers and cartilage matrix deposition during chondrogenesis of BMSC. Endogenous LRF expression was constitutively high in undifferentiated BMSC but remained low in primary articular chondrocytes. Endogenous LRF protein was downregulated in a time-dependent manner during chondrogenesis. BMSCs overexpressing LRF had higher proliferation rates and cell population in the S phase. LRF suppressed p53 expression during chondrogenesis and this might prevent differentiating chondrocytes from entering a quiescent state. Conclusion. Our data showed that LRF is important for stimulating stem cell proliferation and cell cycle progression. It is known that LRF is highly expressed in the mouse limb buds prior to overt chondrogenesis; thus, LRF might function to prevent premature chondrogenic differentiation of stem cells.
机译:目的。癌基因白血病/淋巴瘤相关因子(LRF)可增强软骨肉瘤的增殖和恶性程度。这项研究旨在调查LRF在原代人骨髓间充质干细胞(BMSCs)软骨分化中的作用。设计。通过慢病毒转导,LRF在BMSC中过表达。高密度沉淀培养诱导骨髓间充质干细胞成软骨分化。蛋白质印迹和实时聚合酶链反应分别用于研究软骨形成过程中蛋白质和mRNA水平的变化。番红O染色,免疫组化和糖胺聚糖含量用于评估软骨基质沉积。通过线粒体脱氢酶活性和细胞计数来确定BMSC的增殖。通过流式细胞仪进行细胞周期分析。结果。 LRF的过表达有效抑制BMSC软骨形成过程中软骨细胞标志物的蛋白质和mRNA表达以及软骨基质沉积。内源性LRF表达在未分化的BMSC中组成性较高,但在原发性软骨细胞中仍然较低。软骨形成过程中内源性LRF蛋白以时间依赖性方式下调。过表达LRF的BMSC在S期具有较高的增殖速率和细胞群。 LRF抑制了软骨形成过程中p53的表达,这可能阻止分化的软骨细胞进入静止状态。结论。我们的数据表明LRF对于刺激干细胞增殖和细胞周期进程很重要。众所周知,在明显的软骨形成之前,LRF在小鼠肢芽中高表达。因此,LRF可能起到阻止干细胞过早软骨分化的作用。

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