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FisherbrandTM Sterile Cell Strainers

Company: Fisher Scientific
Catalog#: 22-363-548
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Sleeping Beauty Transposon-based System for Rapid Generation of HBV-replicating Stable Cell Lines
Author:
Date:
2018-07-05
[Abstract]  The stable HBV-transfected cell lines, which based on stable integration of replication-competent HBV genome into hepatic cells, are widely used in basic research and antiviral drug evaluation against HBV. However, previous reported strategies to generate HBV-replicating cell lines, which primarily rely on random integration of exogenous DNA by plasmid transfection, are inefficient and time-consuming. We newly developed an all-in-one Sleeping Beauty transposon system (denoted pTSMP-HBV vector) for robust generation of stable HBV-replicating cell lines of different genotype. The pTSMP-HBV vector contains HBV 1.3-copy genome and dual selection markers (mCherry and puromycin resistance gene), allowing rapid enrichment of stably-transfected cells via red fluorescence-activated cell sorting ... [摘要]  稳定的HBV转染细胞系基于将复制能力的HBV基因组稳定整合到肝细胞中,广泛用于基础研究和针对HBV的抗病毒药物评估。然而,先前报道的产生HBV复制细胞系的策略(其主要依赖于通过质粒转染的外源DNA的随机整合)是低效且耗时的。我们新开发了一体化睡眠美容转座子系统(表示为pTSMP-HBV载体),用于稳定产生不同基因型的稳定HBV复制细胞系。 pTSMP-HBV载体含有HBV1.3拷贝基因组和双重选择标记(mCherry和嘌呤霉素抗性基因),允许通过红色荧光激活细胞分选和嘌呤霉素抗生素选择快速富集稳定转染的细胞。在该方案中,我们描述了构建HBV复制稳定细胞和系统评估这些细胞的HBV复制和病毒蛋白表达谱的详细程序。

【背景】慢性乙型肝炎病毒(HBV)感染目前是一个主要的公共卫生负担,影响全球超过2.4亿人(Witt-Kehati et al。,2016)。慢性HBV患者患慢性活动性肝炎,肝硬化或原发性肝细胞癌(HCC)的风险升高(Schweitzer et al。,2015)。目前用干扰素-α或核苷类似物治疗并不能根除病毒,它们对清除乙型肝炎表面抗原(HBsAg)的作用有限(Lucifora和Protzer,2016; Soriano et al。,2017) 。因此,迫切需要开发新的抗病毒抑制剂(Nassal,2015)。

用于评估新药抗HBV活性的细胞培养模型是新药开发的重要工具。稳定的HBV复制细胞系,携带复制能力的HBV基因组稳定整合到人肝癌细胞系(Huh7和/或HepG2)的基因组中,被广泛用于评估抗病毒药物的作用(Witt-Kehati ...

Osteoblast Sorting and Intracellular Staining of CXCL12
Author:
Date:
2018-05-20
[Abstract]  Osteoblasts are bone marrow endosteum-lining niche cells playing important roles in the regulation of hematopoietic stem cells by secreting factors and cell adhesion molecules. Characterization of primary osteoblasts has been achieved through culture of outgrowth of collagenase treated bone. Immunophenotyping and flow-based analysis of long bone osteoblasts offer a simplified and rapid approach to characterize osteoblasts. We describe a modified procedure of isolating mouse bone marrow osteoblastic cells based on cell surface immunophenotyping. The chemokine CXCL12 (also known as stromal-derived factor, SDF-1) together with its receptor CXCR4 are expressed by osteoblasts and bone marrow stroma cells. The CXCL12-CXCR4 axis is important for hematopoietic stem cell retention to their niches ... [摘要]  成骨细胞是通过分泌因子和细胞粘附分子在调节造血干细胞中发挥重要作用的骨髓内皮细胞生态位细胞。 通过培养胶原酶处理的骨骼的生长已经实现了原代成骨细胞的表征。 长骨成骨细胞的免疫分型和基于流动的分析为表征成骨细胞提供了简化和快速的方法。 我们描述了基于细胞表面免疫分型的分离小鼠骨髓成骨细胞的修改过程。 趋化因子CXCL12(也称为基质衍生因子SDF-1)与其受体CXCR4一起由成骨细胞和骨髓基质细胞表达。 CXCL12-CXCR4轴对于造血干细胞滞留于其生态位(Sugiyama等,2006)和支持白血病启动细胞活性(Pitt等,2015年)。 这里我们描述CXCL12细胞内染色的过程。

【背景】骨髓龛是一种高度组织化的微环境,基质细胞参与与调节HSC静止,分化和动员的造血干细胞(HSC)的直接细胞 - 细胞相互作用(Anthony and Link,2014; Mendelson and Frenette,2014; Morrison和斯卡登,2014年)。 HSC细胞生态位中的多种细胞类型可能以不同的但可能重叠的方式贡献于小生境功能支持。这些细胞包括但不限于成骨细胞,破骨细胞,富含CXCL12的网状(CAR)细胞,Nestin +基质细胞,瘦素受体+(LepR + ...

Isolation and Separation of Epithelial CD34+ Cancer Stem Cells from Tgfbr2-deficient Squamous Cell Carcinoma
Author:
Date:
2017-09-05
[Abstract]  Most epithelial tumors have been shown to contain cancer stem cells that are potentially the driving force in tumor progression and metastasis (Kreso and Dick, 2014; Nassar and Blanpain, 2016). To study these cells in depth, cell isolation strategies relying on cell surface markers or fluorescent reporters are essential, and the isolation strategies must preserve their viability. The ability to isolate different populations of cells from the bulk of the tumor will continue to deepen our understanding of the biology of cancer stem cells. Here, we report the strategy combining mechanical tumor dissociation, enzymatic treatment and flow cytometry to isolate a pure population of epithelial cancer stem cells from their native microenvironment. This technique can be useful to further ... [摘要]  大多数上皮肿瘤已经显示含有可能是肿瘤进展和转移的驱动力的癌症干细胞(Kreso和Dick,2014; Nassar和Blanpain,2016)。 为了深入研究这些细胞,依赖于细胞表面标志物或荧光报告基因的细胞分离策略是必不可少的,分离策略必须保持其活力。 从大部分肿瘤中分离不同细胞群的能力将继续加深我们对癌症干细胞生物学的认识。 在这里,我们报告了结合机械肿瘤解离,酶处理和流式细胞术的策略,从其天然微环境中分离出纯种群的上皮癌干细胞。 该技术可用于进一步功能性地分析癌症干细胞(RNA测序和表观遗传学分析),在培养物中培养它们或在移植测定中直接使用它们。
【背景】肿瘤复发和转移是大多数与癌症有关的死亡的主要原因。恶性肿瘤可能由干细胞群体启动和维持(Nassar和Blanpain,2016; Bonnet和Dick,1997),这些细胞是预防复发的重要治疗靶点(Baumann et al。,2008)。研究表明,鳞状细胞癌由肿瘤干细胞亚群维持,其抗药性,并通过进行自我更新和分化(如正常干细胞)引发肿瘤复发,产生增殖祖细胞,其分化形成肿瘤大部分(Locke et al。,2005; Prince et al。,2007; Malanchi et al。,2008; de Sousa e Melo et ...

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