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Administrative supplement for the flow cytometry cell sorter purchase

Administrative supplement for the flow cytometry cell sorter purchase
购买流式细胞仪细胞分选机的行政补充
批准号:
10582315
负责人:
IGOR B RONINSON
金额:
$24.74万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-07-10 至 2024-04-30

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中文摘要
翻译
南卡罗来纳州大学的COBRE靶向治疗中心(CTT)支持 旨在开发针对各种疾病的新的和更有效的药物类别的研究, 这些药物作用于在疾病中起关键作用的分子和细胞靶点。FACS是一种有效的方法, 收集并分析药物治疗后的各种细胞群。重要的是,细胞可以来自 从动物模型分离的组织或血液。然后可以对分选的群体进行进一步的 分析,如基因表达或免疫细胞标记物分类。CTT中现有的细胞分选机 显微镜和流式细胞仪核心(MFCC)已经使用了19年,有几个局限性 相对于更现代的仪器。很难更改输入单元格的源而不引起 污染,并且来自解离的样品几乎总是污染仪器。去污 困难,并削弱了旧的流体系统。该提案的目的是获得资金, Sony SH 800细胞分选仪该仪器采用一次性微流控芯片,消除了交叉污染 旧仪器遇到的问题。此外,与传统的细胞分选系统相比, 到上一代。有几名调查人员已经对此表示支持 应用程序.他们的应用包括表征乳腺癌动物模型中的浸润免疫细胞 癌症;从发育中的斑马鱼中分选细胞以了解颅面发育的机制;分选 抗生素诱发小鼠早发性结直肠癌模型中结肠菌群和上皮细胞的变化 治疗;和目前的CTT目标项目,收集造血干细胞用于移植研究。 将该仪器添加到MFCC将扩展核心的能力,并帮助CTT实现 其目标是为开发靶向治疗的研究人员提供所需的资源。
英文摘要
The COBRE Center for Targeted Therapeutics (CTT) at the University of South Carolina (UofSC) supports research that seeks to develop new and more effective classes of drugs against various diseases, by aiming these drugs at molecular and cellular targets that play a key role in the disease. FACS is a powerful method to collect and analyze various populations of cells after a drug treatment. Importantly, the cells can be from dissociated tissue or blood from animal models. The sorted populations can then be subjected to further analysis, such as gene expression or immune cell marker classification. The existing cell sorter in the CTT Microscopy and Flow Cytometry Core (MFCC) has been in service for 19 years and has several limitations relative to more modern instrumentation. It is difficult to change the source of input cells without causing contamination, and samples from dissociated almost always contaminates the instrument. Decontamination is difficult and is weakening the old fluidics system. The purpose of this proposal is to acquire funds to purchase a Sony SH800 Cell Sorter. This instrument uses disposable microfluids chips to eliminate the cross-contamination problem experienced with the older instrument. Also, it is much easier to operate and sorts cells faster compared to the previous generation. There are several investigators who have already expressed their support for this application. Their applications include characterizing infiltrating immune cells in an animal model of breast cancer; sorting cells from developing zebrafish to understand mechanisms of craniofacial development; sorting the microbiota and epithelial cells of colon in a mouse model of early onset colorectal cancer caused by antibiotic treatment; and a current CTT-target project, collect hematopoietic stem cells to use in transplantation studies. The addition of this instrument to the MFCC will expand the capability of the core and help the CTT to achieve its goals to provide needed resources to investigators developing targeted therapeutics.
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