Cellular and Molecular Physiology Core
Cellular and Molecular Physiology Core
批准号:
10048271
负责人:
Mario Strazzabosco
金额:
$31.42万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
未结题
起止时间:
1997-09-30 至 2026-02-28
关键词:
AcetaminophenAdenovirus InfectionsAdultAnimal ModelAnimalsAwardBile fluidCRISPR/Cas technologyCannulationsCell Culture TechniquesCell LineCell SeparationCell modelCellsCholestasisCirrhosisClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsCollagenCollectionComplementary DNAConsultationsContractsCore FacilityCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorDetectionDimethylnitrosamineDiseaseDisease modelDoctor of PhilosophyEndothelial CellsEndotheliumEnsureEnzyme-Linked Immunosorbent AssayEquipmentEquus caballusExperimental ModelsFibroblastsFibrosisFluorescenceGelGene ExpressionGenotypeHepG2HepaticHepatocyteHumanHuman ResourcesImageKidney DiseasesKnockout MiceKupffer CellsLibrariesLiceLigationLiverLiver diseasesLymphocyteMaintenanceMethodsModelingMolecularMusMutateObstructionOperative Surgical ProceduresOrganoidsPartial HepatectomyPatientsPhysiologyPortal vein structurePreparationPrimary Cell CulturesProceduresProductivityProteinsQuality ControlRNARattusReaderRecording of previous eventsReperfusion InjuryReproducibilityResearchResearch PersonnelResourcesReverse Transcriptase Polymerase Chain ReactionRodentSamplingServicesSmall Interfering RNAStandardizationSupervisionSystemTechnical ExpertiseThioacetamideTimeTissuesTrainingTransfectionUpdateViral VectorWorkacute liver injurybile ductcell preparationcholangiocytecostcost effectiveexperienceimaging detectionimaging systeminduced pluripotent stem cellinnovationinterestluminescencemembermonolayermouse modelnovelprimary sclerosing cholangitisprotein expressionstellate cellsynergismtoolvector
中文摘要
项目概要-细胞分子生理学核心
细胞和分子生理学核心是该中心的“工作马”,但它也继续作为
一个创新中心,为肝脏研究人员提供最新的实验模型。核心是
组织向肝脏中心研究者提供技术专业知识、设备和人员,
为他们提供最先进的细胞和分子研究资源,
成本效益的方式。核心在开发用于肝脏研究的新细胞和动物模型方面有着悠久的历史。
目前,核心分为两个部分:(1)细胞分离和细胞培养部分和(2)
分子组成部分。(a)分离的细胞制剂,包括:肝细胞,
胆管细胞、内皮细胞、星状细胞、门静脉成纤维细胞和肝淋巴细胞,主要来自小鼠
还有老鼠当可用时,也使用人肝细胞。超过3,400个分离的细胞被分离。
(B)用于短期和长期培养的细胞培养设施,
(c)使用定量RT-PCR和红外成像检测的蛋白质和基因表达;(d)改变
使用siRNA转染、腺病毒感染和
CRISPR技术;(e)提供各种肝病动物模型和(f)疾病特异性小鼠模型
和人肝类器官,来源于iPSC、胆汁和原代肝组织。通过集中这些程序
在核心设施中,成本和工作量大大减少,调查人员得到高度严谨保证,
可重复性和质量控制,并且制剂通常可以由多个人同时使用。
调查员Mario Strazzabosco,医学博士,博士,拥有超过25年的相关经验,
核心与合作的名誉董事,詹姆斯L。博耶,医学博士,谁拥有超过40年的
这些准备工作和程序的工作经验。他们由Romina Fiorotto博士协助,
蔡世英博士,确保日常监督,可用性,并为研究者提供建议,其中许多
服务
英文摘要
PROJECT SUMMARY – CELLULAR MOLECULAR PHYSIOLOGY CORE
The Cellular and Molecular Physiology Core is the “work horse” of this Center, but it also continues to serve as
an innovation hub to provide liver investigators with the most up-to-date experimental models. The core is
organized to provide technical expertise, equipment and personnel to Liver Center Investigators in order to
provide them with state of the art cell and molecular research resources in an efficient, quality-controlled and
cost-effective manner. The Core has a long history of developing new cell and animal models for liver research.
Currently, the Core is divided into two Components: (1) The Cell Isolation and Cell Culture Component and (2)
The Molecular Component. These are subdivided into: (a) Isolated cell preparations, including: hepatocytes,
cholangiocytes, endothelial cells, stellate cells, portal fibroblasts and hepatic lymphocytes, primarily from mice
and rats. Human hepatocytes are also utilized when available. Over 3,400 separate cell isolations were
performed during the current award period; (b) Cell culture facilities for short and long-term cultures and cell
lines; (c) Protein and gene expression using Quantitative RT-PCR and Infrared imaging detection; (d) Altering
gene expression in liver-related cells, cell lines and tissues using siRNA transfection, adenovirus infection, and
CRISPR technologies; (e) providing a variety of animal models of liver disease and (f) disease-specific mouse
and human liver organoids, derived from iPSC’s, bile, and primary liver tissue. By centralizing these procedures
in a Core facility, cost and effort are dramatically reduced, investigators are assured of a high degree of rigor,
reproducibility, and quality control, and preparations can often be used simultaneously by more than one
investigator. Mario Strazzabosco, MD, PhD, who has more than 25 years of relevant experience, directs this
core with the collaboration of the Emeritus Director, James L. Boyer, MD, who has more than 4 decades of
experience working with these preparations and procedures. They are assisted by Romina Fiorotto, PhD, and
Shi-Ying Cai, PhD, which assures daily supervision, availability, and advice to investigators for many of these
services.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Cross talk between epithelial, inflammatory and mesenchymal cells in the development of portal fibrosis
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批准号:10364642
-
项目类别:
-
资助金额:$50.86万
-
财政年份:2015
-
负责人:Mario Strazzabosco
-
依托单位:
Cross talk between epithelial, inflammatory and mesenchymal cells in the development of portal fibrosis
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批准号:9884664
-
项目类别:
-
资助金额:$51.0万
-
财政年份:2015
-
负责人:Mario Strazzabosco
-
依托单位:
Cross talk between epithelial, inflammatory and mesenchymal cells in the development of portal fibrosis
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批准号:10573163
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项目类别:
-
资助金额:$50.45万
-
财政年份:2015
-
负责人:Mario Strazzabosco
-
依托单位:
CFTR modulates innate immune response in biliary epithelium: Role in the pathogenesis and treatment of Cystic-Fibrosis-related liver disease.
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批准号:10454325
-
项目类别:
-
资助金额:$54.19万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
Liver disease in CF: CFTR controls innate immunity in biliary epithelium
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批准号:8504485
-
项目类别:
-
资助金额:$36.19万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
CFTR modulates innate immune response in biliary epithelium: Role in the pathogenesis and treatment of Cystic-Fibrosis-related liver disease.
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批准号:9982301
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项目类别:
-
资助金额:$56.09万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
CFTR modulates innate immune response in the biliary epithelium. Role in the path
-
批准号:8656679
-
项目类别:
-
资助金额:$36.21万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
CFTR modulates innate immune response in the biliary epithelium. Role in the path
-
批准号:8836532
-
项目类别:
-
资助金额:$36.21万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
CFTR modulates innate immune response in biliary epithelium: Role in the pathogenesis and treatment of Cystic-Fibrosis-related liver disease.
-
批准号:10223271
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项目类别:
-
资助金额:$55.12万
-
财政年份:2013
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Polycystic Diseases of the Liver
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批准号:7775140
-
项目类别:
-
资助金额:$33.02万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Biliary Pathophysiology and in Polycystic Dise
-
批准号:8882404
-
项目类别:
-
资助金额:$36.21万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Polycystic Diseases of the Liver
-
批准号:8228110
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项目类别:
-
资助金额:$32.44万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Biliary Pathophysiology and in Polycystic Dise
-
批准号:8629435
-
项目类别:
-
资助金额:$36.21万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Polycystic Diseases of the Liver
-
批准号:7591748
-
项目类别:
-
资助金额:$33.1万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Biliary Pathophysiology and in Polycystic Dise
-
批准号:8737227
-
项目类别:
-
资助金额:$36.21万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Epithelial Angiogenic Signaling in Polycystic Diseases of the Liver
-
批准号:8053839
-
项目类别:
-
资助金额:$32.44万
-
财政年份:2008
-
负责人:Mario Strazzabosco
-
依托单位:
Cellular and Molecular Physiology Core
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批准号:10584506
-
项目类别:
-
资助金额:$29.67万
-
财政年份:1997
-
负责人:Mario Strazzabosco
-
依托单位:
Cellular and Molecular Physiology Core
-
批准号:10374708
-
项目类别:
-
资助金额:$29.67万
-
财政年份:1997
-
负责人:Mario Strazzabosco
-
依托单位:
海外基金