Flow Cytometry CORE
流式细胞术核心
基本信息
- 批准号:10020070
- 负责人:
- 金额:$ 32.24万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:
- 资助国家:美国
- 起止时间:至
- 项目状态:未结题
- 来源:
- 关键词:1 year oldAffectAgeApoptosisAutoimmunityBindingBloodBudgetsCNS autoimmunityCellsChoroidal NeovascularizationClinicalCollaborationsCommunitiesComplexComputer softwareDNADataData AnalysesDetectionDevelopmentDrug resistanceEducationElementsEquipmentEyeFamily suidaeFlow CytometryFoundationsGene ExpressionGenetic TranscriptionGenotypeGrantHourHumanIndividualInformation TechnologyInstitutesIntramural N.I.H. Research SupportInvestmentsJournalsLaboratoriesLeukocytesLiquid substanceMalignant NeoplasmsMeasurementMediatingMembraneMethodsMicrogliaMonitorMuscle CellsNational Eye InstituteNational Institute of Allergy and Infectious DiseaseNational Institute of Child Health and Human DevelopmentNational Institute on Deafness and Other Communication DisordersPeripheral Blood Mononuclear CellPhenotypePloidiesPopulationPostdoctoral FellowPreparationPrincipal InvestigatorProceduresProductionProteinsProtocols documentationPublicationsRegulatory T-LymphocyteReporter GenesResearchResearch PersonnelResearch Project GrantsResourcesRetinalRetinal DegenerationRodentSamplingScienceServicesSignal TransductionSorting - Cell MovementSourceSpecimenStainsStem cellsStructure of retinal pigment epitheliumStudentsSupervisionTechniquesTh1 CellsTissuesTrainingUnited States National Institutes of HealthWorkautoimmune uveitiscytokinedata acquisitionequipment acquisitionhuman tissueinhibitor/antagonistinstrumentinstrumentationinterleukin-22neuropathologyoperationpromoterprostate cancer cellrecruitresponsesquare footstemnessvolunteer
项目摘要
GENERAL OVERVIEW:
The Flow Cytometry Core at NEI provides flow cytometry analytical and sorting equipment and services to the NEI Intramural community. It utilizes and develops state-of-the-art sample preparation, data acquisition and analysis, and sorting procedures in collaborative research projects. Provides training to students, fellows, and principal investigators on sample preparation, staining, and post-sort handling. Assesses technical research needs and recommends recruitment of the appropriate staff and acquisition of the equipment needed to meet those needs. The core also supports NIH intramural research outside NEI by processing samples for laboratories without access to flow cytometry instrumentation and collaborations with the Foundation for Advanced Education in the Sciences
SERVICES PROVIDED THE CORE:
This year, 63 (sixty-three) individuals from 13 (thirteen) different laboratories used the facility. These services and collaborative services were performed for 12 Principal Investigators (PIs) from 8 NEI labs (ERPD, LI, LRCMB, MSF, N-NRL, RN, OGVFB and UNGIRD), plus 4 PIs from 4 other institutes at NIH (NCI, NIAID, NICHD and NIDCD). This year the core performed 1,250 hours of sorting and over 15,000 samples were analyzed.
Among the techniques now in use within the core are methods for phenotyping live cells, gene expression detection through fluorescent reporter genes, monitoring membrane and DNA content changes due to apoptosis or proliferation, measurement of intracellular proteins and quantification of soluble proteins.
The work involving human tissues includes the sorting of peripheral blood mononuclear cells to study their cytokine production, genotype and DNA or RNA expression. The sources are blood, buffy coat, and white cells. Some analytical work had been done with eye fluids, eye tissue specimen, protein, and tears. The National Eye Institute made a great investment in biosafety with the addition BD FACSAria Fusion flow cytometer equipped with a fully integrated biosafety cabinet. This sorter meets the recent NIH's operator and sample protection requirements as well as global standards for bioprotection for processing human samples. No human tissues were stored by the core.
The Core encourages, but does not require, users to acknowledge the Core contribution in their publications. The following are examples of the publications that used NEI Flow Cytometry Core resources:
Ma W, et al. Absence of TGF signaling in retinal microglia induces retinal degeneration and exacerbates choroidal neovascularization. eLife. 2019;8:e42049.
Sharma R, et al. Clinical-grade stem cell-derived retinal pigment epithelium patch rescues retinal degeneration in rodents and pigs. Sci Transl Med. 2019 Jan 16;11(475). pii: eaat5580. doi: 10.1126/scitranslmed.aat5580.
Uygur B et al. Interactions with Muscle Cells Boost Fusion, Stemness, and Drug Resistance of Prostate Cancer Cells. Mol Cancer Res. 2019 Mar;17(3):806-820. doi: 10.1158/1541-7786.MCR-18-0500. Epub 2018 Dec 26.
Mary J. Mattapallil, et al. Interleukin 22 ameliorates neuropathology and protects from central nervous system autoimmunity,Journal of Autoimmunity,Volume 102,
2019,Pages 65-76, ISSN 0896-8411.
So Jin Bing et al. AS101 ameliorates experimental autoimmune uveitis by regulating Th1 and Th17 responses and inducing Treg cells. Journal of Autoimmunity Volume 100, June 2019, Pages 52-61
Cancan Lyu et al. TMP778, a selective inhibitor of RORt, suppresses experimental autoimmune uveitis development, but affects both Th17 and Th1 cell populations. Eur. J. Immunol.48-11 0014-2980 doi:10.1002/eji.201747029
ChengRong Yu, et al. Production of IL35 by Bregs is mediated through binding of BATFIRF4IRF8 complex to il12a and ebi3 promoter elements. J Leukoc Biol 104 6 0741-5400 doi:10.1002/JLB.3A0218-071RRR
TRAINING:
Several formal training sessions were offered by the Core to the NEI community. These courses included: Introduction to Flow Cytometry, Advanced Techniques (Ex. Apoptosis applications), Analytical Instrument Operation and Data Analysis with FloJo Software.
The Core stuff received about 100 hrs. or training a year in flow cytometry.
The Core stuff provided about 50 hrs of training to the NEI community and 60 hrs of training through FAES to the NIH community.
总体概述:
NEI 的流式细胞术核心为 NEI 校内社区提供流式细胞术分析和分选设备及服务。它在合作研究项目中利用和开发最先进的样品制备、数据采集和分析以及分类程序。为学生、研究员和主要研究人员提供样品制备、染色和分选后处理方面的培训。评估技术研究需求并建议招聘适当的人员并采购满足这些需求所需的设备。该核心还支持 NEI 之外的 NIH 校内研究,为无法使用流式细胞术仪器的实验室处理样本,并与科学高级教育基金会合作
提供的服务核心:
今年,来自 13(十三)个不同实验室的 63(六十三)个人使用了该设施。这些服务和协作服务是为来自 8 个 NEI 实验室(ERPD、LI、LRCMB、MSF、N-NRL、RN、OGVFB 和 UNGIRD)的 12 名首席研究员 (PI) 以及来自 NIH 4 个其他研究所(NCI、 NIAID、NICHD 和 NIDCD)。今年,核心进行了 1,250 小时的分选,分析了超过 15,000 个样本。
目前核心使用的技术包括活细胞表型分析方法、通过荧光报告基因检测基因表达、监测细胞凋亡或增殖导致的膜和 DNA 含量变化、测量细胞内蛋白质以及定量可溶性蛋白质。
涉及人体组织的工作包括分选外周血单核细胞,以研究其细胞因子的产生、基因型以及 DNA 或 RNA 表达。来源是血液、血沉棕黄层和白细胞。对眼液、眼组织样本、蛋白质和眼泪进行了一些分析工作。美国国家眼科研究所在生物安全方面进行了大量投资,新增了配备完全集成生物安全柜的 BD FACSAria Fusion 流式细胞仪。该分选机满足最近 NIH 的操作员和样品保护要求以及处理人体样品的生物保护全球标准。核心中没有储存任何人体组织。
核心鼓励但不要求用户在其出版物中承认核心的贡献。以下是使用 NEI 流式细胞术核心资源的出版物示例:
马伟,等。视网膜小胶质细胞中TGF信号传导的缺失会诱导视网膜变性并加剧脉络膜新生血管形成。电子生活。 2019;8:e42049。
夏尔马 R 等人。临床级干细胞来源的视网膜色素上皮补片可挽救啮齿动物和猪的视网膜变性。科学翻译医学。 2019 年 1 月 16 日;11(475)。 PII:eaat5580。 doi:10.1126/scitranslmed.aat5580。
维吾尔 B 等。与肌肉细胞的相互作用促进前列腺癌细胞的融合、干性和耐药性。摩尔癌症研究中心。 2019 年 3 月;17(3):806-820。 DOI:10.1158/1541-7786.MCR-18-0500。电子版 2018 年 12 月 26 日。
玛丽·J·马塔帕利 (Mary J. Mattapallil) 等人。白细胞介素 22 改善神经病理学并预防中枢神经系统自身免疫,自身免疫杂志,第 102 卷,
2019 年,第 65-76 页,ISSN 0896-8411。
所以金兵等人。 AS101 通过调节 Th1 和 Th17 反应并诱导 Treg 细胞来改善实验性自身免疫性葡萄膜炎。 《自身免疫杂志》第 100 卷,2019 年 6 月,第 52-61 页
坎坎·吕等人。 TMP778 是一种 RORt 选择性抑制剂,可抑制实验性自身免疫性葡萄膜炎的发展,但会影响 Th17 和 Th1 细胞群。欧元。 J.免疫学杂志.48-11 0014-2980 doi:10.1002/eji.201747029
于成荣,等。 Bregs 产生 IL35 是通过 BATFIRF4IRF8 复合物与 il12a 和 ebi3 启动子元件的结合介导的。 J Leukoc Biol 104 6 0741-5400 doi:10.1002/JLB.3A0218-071RRR
训练:
核心向 NEI 社区提供了几次正式培训课程。这些课程包括:流式细胞术简介、先进技术(例如细胞凋亡应用)、分析仪器操作和使用 FloJo 软件进行数据分析。
核心内容花了大约 100 小时。或接受一年的流式细胞术培训。
核心人员为 NEI 社区提供了大约 50 小时的培训,并通过 FAES 为 NIH 社区提供了 60 小时的培训。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Rachel R. Caspi其他文献
Methimazole protects from experimental autoimmune uveitis (EAU) by inhibiting antigen presenting cell function and reducing antigen priming
甲硫咪唑通过抑制抗原呈递细胞功能和减少抗原启动来预防实验性自身免疫性葡萄膜炎 (EAU)
- DOI:
- 发表时间:
2003 - 期刊:
- 影响因子:5.5
- 作者:
Peng Wang;Shu‐hui Sun;P. Silver;C. Chan;R. Agarwal;B. Wiggert;L. Kohn;G. A. Jamieson;Rachel R. Caspi - 通讯作者:
Rachel R. Caspi
Rachel R. Caspi的其他文献
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{{ truncateString('Rachel R. Caspi', 18)}}的其他基金
Genetic, Cellular And Molecular Mechanisms In Autoimmune
自身免疫的遗传、细胞和分子机制
- 批准号:
6826498 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular and Molecular Mechanisms in Autoimmunity to Retina
视网膜自身免疫的遗传、细胞和分子机制
- 批准号:
8556803 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular and Molecular Mechanisms in Autoimmunity to Retina
视网膜自身免疫的遗传、细胞和分子机制
- 批准号:
10706090 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular and Molecular Mechanisms in Autoimmunity to Retina
视网膜自身免疫的遗传、细胞和分子机制
- 批准号:
7734587 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular and Molecular Mechanisms in Autoimmunity to Retina
视网膜自身免疫的遗传、细胞和分子机制
- 批准号:
10019973 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular And Molecular Mechanisms In Autoimmune
自身免疫的遗传、细胞和分子机制
- 批准号:
7321836 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
Genetic, Cellular and Molecular Mechanisms in Autoimmunity to Retina
视网膜自身免疫的遗传、细胞和分子机制
- 批准号:
8737605 - 财政年份:
- 资助金额:
$ 32.24万 - 项目类别:
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