CORE--CELLULAR NEUROSCIENCE CORE
核心--细胞神经科学核心
基本信息
- 批准号:7670394
- 负责人:
- 金额:$ 25.53万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2008
- 资助国家:美国
- 起止时间:2008-07-01 至 2010-06-30
- 项目状态:已结题
- 来源:
- 关键词:Animal ModelAnimalsArtsBiochemistryBiologyBrainCell Culture TechniquesCell physiologyCellsChildhoodChildhood Brain NeoplasmColorComplementConditionConfocal MicroscopyConsultationsCounselingCultured CellsDataDepthDevelopmentDevelopmental DisabilitiesDiseaseDoctor of MedicineDoctor of PhilosophyElectrophysiology (science)EmbryoEnsureEpilepsyEquipmentEvolutionFunctional disorderFundingGenerationsGenesGeneticGenotypeGoalsGrowthHeadHistopathologyHumanHuman ResourcesImageImageryIn Situ HybridizationInstitutionInterdisciplinary StudyInvestmentsLasersLeadershipLifeMental RetardationMental Retardation and Developmental Disabilities Research CentersMethodsMicroscopeMicroscopyMissionMitochondriaModelingMolecularMolecular GeneticsMutagenesisNatural regenerationNeuraxisNeurodegenerative DisordersNeurologistNeuronsNeurosciencesPathogenesisPathologyPediatric Brain InjuryPediatric HospitalsPeripheralPhenotypePhysiologicalPoliciesProductivityProteinsPublicationsPurposeReagentResearch InstituteResearch PersonnelServicesSpecimenSpectrum AnalysisStagingSurveysSystemTechniquesTechnologyTissuesTransgenic OrganismsWorkbaseexperiencegene discoveryinnovationinstrumentinstrumentationinterestmembermicromanipulatorneurochemistryneuropathologynew technologynoveloptical imagingpleasureresponsesatisfactionskillstissue preparationtumor
项目摘要
The initial (1999) application did not include a Cellular Neuroscience Core. Instead, it proposed separate cores
in Neuropathology and Neuroscience, with the latter offering expertise in cell culture. The Director of the
Neuroscience Core was David Pleasure, M.D., an internationally recognized neurologist with interests in glial
biology of the peripheral and central nervous system. Neuropathology initially was headed by John
Trojanowski, M.D., Ph.D. and Dr. Lucy Rorke, M.D., distinguished neuropathologists with respective eminence
in neurodegenerative diseases and pediatric brain tumors. As user needs evolved, it became apparent that these
facilities should be merged into a single Cellular Neuroscience Core. This was accomplished in 1994 with Dr.
Pleasure as the Director. He served in this capacity through the renewal of the Center (1999) until 2001, when
leadership passed to Dr. Jeffrey Golden, a pediatric neuropathologist with a primary interest in brain
development and its disorders. Dr. Golden first joined CHOP in 1997 and immediately became engaged with
the MRDDRC, both as a user and as an Associate Director of the Cellular Neuroscience Core. Dr. Pleasure has
continued to serve as the Director of the Stokes Research Institute at CHOP.
Since its inception (1994) our Core has provided users with a diverse repertoire of state-of-the-art methods for
visualization of the distributions of gene products in normal, developing neural cells and in those undergoing
various forms of degeneration and regeneration. We have continually and eagerly added new skills,
instrumentation and reagents to better serve our users's needs. In 1995, with the generous assistance of the
Children's Hospital, we purchased a Leica confocal microscope to which we added inverted microscopy, stagemounted
micromanipulators/microinjectors, and a stage-mounted environmental chamber, thus permitting
prolonged observation and manipulation of living cells under physiological conditions. In this manner we
offered 8-color capacity fluorescent imaging. Our institution paid for the apparatus and we used MRDDRC
funding to partially support a technician who worked with Dr. Peter Bannerman, the Director of Confocal
Microscopy. Dr. Bannerman became very skillful in the use of this instrument and he made this valuable
expertise available to MRDDRC researchers.
We made several other notable technological additions to the Core repertoire, including in situ hybridization in
both sections and whole embryos. Our general purpose has been not only to make available a technology, but a
consultative service that facilitates implementation of the method as well as the interpretation of data. We
adhered to this policy when we also added video-enhanced microscopy in order to better support MRDDRC
investigators in analyzing intracellular Ca2+ and Na+ as well as the estimate of mitochondrial potential.
We were especially gratified that Dr. Douglas Coulter joined the Core upon his coming to CHOP in 1999. Dr.
Coulter added to our "armamentarium" his deep experience in electrophysiology and his background in
studying the epilepsies. We also welcomed (2003) Dr. Alex Judkins, a pediatric neuropathologist with interests
in pediatric brain injury and pediatric brain tumors v atypical teratoid/rhabadoid tumors and primative
neuroectodermal tumors in particular. Supported by funds from the Department of Pathology and CHOP, Dr.
Judkins oversees the newly equipped histopathology labs tissue microarrayer and laser-capture microscopy
systems. These systems, which are now being utilized by center investigators, will also complement services
provided by the Molecular Genetics core and the Analytical Neurochemistry cores.
Advances in genetics have rapidly accelerated the discovery of genes implicated in the pathogenesis of the
developmental disabilities, including several genes that have been identified by members of our MRDDRC. To
better appreciate genotype-phenotype relationships, the Cellular Neuroscience Core plans to offer transgenic
and mutagenesis services during the next funding period. The goal is to generate animal models for the specific
intent to study disorders relevant to the MRDDRC mission. Dr. Golden has overseen the establishment of a core
at CHOP to perform these services. The MRDDRC plans to provide consultation and economical access to this
new facility. This exciting advance will help investigators to scrutinize the basis of disease in hitherto
inaccessible detail. Indeed, we note with satisfaction that MRDDRC users will explore these models not only
with the techniques that our Core offers, but with the plethora of methods that are available through the
Molecular Genetics and Analytical Neurochemistry and Spectroscopy Cores.
As a result of the continued evolution of this core and the investment by the institution in new technologies and
the constant upgrading of equipment, the Cellular Neuroscience Core has been able to provide outstanding
services to Center users. Over the past 4.5 years we have serviced 25 investigators; contributing to at least 49
publications. The growth of existing services and the addition of new methods ensures that MRDDRC members
enjoy ready access to that technological array that has become so essential to all contemporary interdisciplinary
research.
最初(1999年)的申请不包括细胞神经科学核心。相反,它提出了单独的核心
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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David E. Pleasure其他文献
Tissue culture analysis of neurogenesis: Myelination and synapse formation are retarded by serum deprivation
- DOI:
10.1016/0006-8993(78)90792-8 - 发表时间:
1978-04-21 - 期刊:
- 影响因子:
- 作者:
Seung U. Kim;David E. Pleasure - 通讯作者:
David E. Pleasure
David E. Pleasure的其他文献
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{{ truncateString('David E. Pleasure', 18)}}的其他基金
Nanoparticle-mediated delivery of a base editor for in utero treatment of Canavan Disease
纳米颗粒介导的碱基编辑器递送用于子宫内治疗卡纳万病
- 批准号:
10727872 - 财政年份:2023
- 资助金额:
$ 25.53万 - 项目类别:
Manipulating N-acetyl-L-aspartate transport to treat Canavan leukodystrophy
操纵 N-乙酰基-L-天冬氨酸转运来治疗 Canavan 脑白质营养不良
- 批准号:
10406711 - 财政年份:2022
- 资助金额:
$ 25.53万 - 项目类别:
Manipulating N-acetyl-L-aspartate transport to treat Canavan leukodystrophy
操纵 N-乙酰基-L-天冬氨酸转运来治疗 Canavan 脑白质营养不良
- 批准号:
10554428 - 财政年份:2022
- 资助金额:
$ 25.53万 - 项目类别:
Manipulating N-acetyl-L-aspartate to reverse Canavan leukodystrophy
操纵 N-乙酰基-L-天冬氨酸逆转 Canavan 脑白质营养不良
- 批准号:
10026520 - 财政年份:2020
- 资助金额:
$ 25.53万 - 项目类别:
CANAVAN DISEASE: SUPPRESSING THE PHENOTYPE BY INHIBITING NAA SYNTHESIS
CANAVAN 病:通过抑制 NAA 合成来抑制表型
- 批准号:
8965565 - 财政年份:2015
- 资助金额:
$ 25.53万 - 项目类别:
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