Histology and Tissue Characterization
组织学和组织表征
基本信息
- 批准号:7678116
- 负责人:
- 金额:$ 17.64万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-07-01 至 2014-06-30
- 项目状态:已结题
- 来源:
- 关键词:Animal ExperimentationAnimal ModelAnimalsAntibodiesArchivesArtificial skinBiologyClinicalCollaborationsCore FacilityCutaneousDataDermatologyDiseaseEmbryoEnsureEquipmentEvaluationFormalinFundingGenetically Engineered MouseHistologicHistologyHumanHuman ResourcesImmunohistochemistryIn Situ HybridizationInstructionLaboratoriesLinkMessenger RNAMethodologyMicroscopicModelingMolecularMusParaffin EmbeddingPennsylvaniaPhenotypeProcessProteinsProtocols documentationRNAResearchResearch InfrastructureResearch PersonnelResearch Project GrantsSamplingSectioning techniqueServicesSkinSkin TissueSpecimenStaining methodStainsTechniquesTimeTissuesTrainingUnited States National Institutes of HealthUniversitiesWorkXenograft procedurebasebiological researchcostcost effectivenesscost efficientexperiencehuman diseasehuman tissuekeratinocytemembermouse modelmutantnovelsound
项目摘要
The Skin Histology and Characterization Core (SHCC) will provide SDRC investigators with services to
aid them in the histopathologic and molecular characterization of skin samples derived from animal models,
primarily mutant or genetically engineered mice. In addition, this core will provide sectioning and
histopathological analysis of de-identified, formalin fixed, paraffin embedded dermatopathology archived
samples provided by Core B. The aims of the SHCC are: 1) To provide expert service in the processing,
embedding, sectioning, and staining of skin specimens from research animals, including murine embryos,
and sectioning and staining of archived, de-identified human tissue; 2) To provide expert service and
training in protein immunohistochemical staining using skin samples; to establish and provide advice in
determining effective staining protocols for novel antibodies; 3) To provide expert service and training for
RNA in situ hybridization of skin samples using radioisotopic and colorimetric methodologies; 4) To provide
expert interpretation and training in the histopathological evaluation of animal and human skin histology. We
will ensure accurate correlations between animal model phenotypes and human diseases.
The SHCC will build upon the existing laboratory infrastructure operating in the Department of Dermatology
to enhance cutaneous biology research at the University of Pennsylvania. The proposed SHCC will be a
shared facility that will help investigators conduct their independently NIH funded research projects in a more
time- and cost-efficient manner. The SHCC will consolidate manpower and promote cost-effectiveness by
providing high quality services at a lower cost than if each investigator were to attempt to establish these
analytical techniques individually. The SHCC services will help SDRC investigators characterize the
phenotype of their genetically engineered mouse models at the histologic, protein, and mRNA levels, and
then correlate this data with relevant human diseases. Such services are critical for generating sound
scientific hypotheses linking animal models with human diseases. The SHCC will interact closely with Core B
in coordinating the staining and analysis of archived dermatopathology specimens. To assure high quality
service, the SHCC will establish an oversight committee. The SHCC will also interact with Core C by
providing histologic, immunohistochemical, and mRNA in situ hybridization analysis of reconstituted skin and
keratinocyte xenografts produced by this core. These services will attract established investigators to
cutaneous biology and assist young investigators in obtaining important data for their research projects.
RELEVANCE (See instructions):
The Skin Histology and Characterization Core will facilitate research on cutaneous diseases by providing
cost-effective, high quality services for skin tissue that include the following: processing, staining, protein
immunohistochemistry, mRNA in situ hybridization, and histologic evaluation. These services will allow
investigators to effectively correlate the cutaneous phenotype of an animal model with a human disease.
皮肤组织学和表征核心(SHCC)将为SDRC研究者提供以下服务:
帮助他们对来自动物模型的皮肤样本进行组织病理学和分子表征,
主要是突变或基因工程小鼠。此外,该核心将提供切片和
组织病理学分析去识别,福尔马林固定,石蜡包埋皮肤病理学存档
样品由岩心B提供。SHCC的目标是:1)在处理过程中提供专家服务,
对来自研究动物的皮肤标本进行包埋、切片和染色,包括鼠胚胎,
以及对存档的、去识别的人体组织进行切片和染色; 2)提供专家服务,
使用皮肤样本进行蛋白质免疫组织化学染色的培训;建立并提供建议,
确定新型抗体的有效染色方案; 3)为以下人员提供专家服务和培训:
使用放射性同位素和比色方法对皮肤样品进行RNA原位杂交; 4)提供
在动物和人类皮肤组织学的组织病理学评价方面提供专家解释和培训。我们
将确保动物模型表型和人类疾病之间的准确相关性。
SHCC将建立在皮肤科现有的实验室基础设施上
来加强宾夕法尼亚大学的皮肤生物学研究。拟议的SHCC将是一个
共享设施,这将有助于研究人员进行他们的独立国家卫生研究院资助的研究项目,在一个更
时间和成本效益的方式。小组委员会会整合人手,提高成本效益,
以较低的成本提供高质量的服务,而不是每个研究者试图建立这些
个别分析技术。SHCC服务将帮助SDRC调查人员描述
其基因工程小鼠模型在组织学、蛋白质和mRNA水平上的表型,以及
然后将这些数据与相关的人类疾病联系起来。这些服务对于产生声音至关重要
将动物模型与人类疾病联系起来的科学假说。SHCC将与核心B密切互动
协调对存档的皮肤病理学标本的染色和分析。确保高质量
根据该计划,SHCC将成立一个监督委员会。SHCC还将通过以下方式与核心C进行互动:
提供重建皮肤的组织学、免疫组织化学和mRNA原位杂交分析,
角质细胞异种移植物产生的核心。这些服务将吸引知名调查人员,
皮肤生物学和协助年轻的研究人员获得重要的数据,为他们的研究项目。
相关性(参见说明):
皮肤组织学和表征核心将通过提供
具有成本效益的高质量皮肤组织服务,包括以下内容:处理,染色,蛋白质
免疫组织化学、mRNA原位杂交和组织学评价。这些服务将允许
研究人员将有效地将动物模型的皮肤表型与人类疾病相关联。
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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John T. Seykora其他文献
Penn Academy for Skin Health (PASH): An Experiential Pipeline Program in Skin Biology and Dermatology for High-School Students
宾夕法尼亚皮肤健康学院(PASH):面向高中生的皮肤生物学和皮肤病学体验式培养计划
- DOI:
10.1016/j.jid.2024.05.036 - 发表时间:
2025-03-01 - 期刊:
- 影响因子:5.700
- 作者:
Elizabeth A. Grice;Donna Brennan-Crispi;Natalia Rodriguez;David J. Margolis;John T. Seykora;George Cotsarelis;Susan C. Taylor;Jamie Shuda - 通讯作者:
Jamie Shuda
Laser Capture Microdissection-based RNAseq for Profiling Mouse and Human Sebaceous Gland Transcriptomes.
基于激光捕获显微切割的 RNAseq 用于分析小鼠和人类皮脂腺转录组。
- DOI:
- 发表时间:
2023 - 期刊:
- 影响因子:6.5
- 作者:
Jordan C. Harris;Stephen Prouty;Molly A Nelson;Derek C. Sung;Amanda M. Nelson;John T. Seykora;Taku Kambayashi;Elizabeth A. Grice - 通讯作者:
Elizabeth A. Grice
Acetyl-CoA synthesis in the skin is a key determinant of systemic lipid homeostasis
皮肤中乙酰辅酶 A 的合成是全身脂质稳态的关键决定因素。
- DOI:
10.1016/j.celrep.2025.115284 - 发表时间:
2025-02-25 - 期刊:
- 影响因子:6.900
- 作者:
Phuong T.T. Nguyen;Mia Shiue;Nina Kuprasertkul;Pedro Costa-Pinheiro;Luke T. Izzo;Laura V. Pinheiro;Hayley A. Affronti;Gabriel Gugiu;Shivani Ghaisas;Joyce Y. Liu;Jordan C. Harris;Charles W. Bradley;John T. Seykora;Xiaolu Yang;Taku Kambayashi;Clementina Mesaros;Brian C. Capell;Kathryn E. Wellen - 通讯作者:
Kathryn E. Wellen
Central centrifugal cicatricial alopecia in males
- DOI:
10.1016/j.jaad.2023.07.1011 - 发表时间:
2023-12-01 - 期刊:
- 影响因子:
- 作者:
Tiaranesha K. Jackson;Yacine Sow;Katherine Omueti Ayoade;John T. Seykora;Susan C. Taylor;Temitayo Ogunleye - 通讯作者:
Temitayo Ogunleye
Central centrifugal cicatricial alopecia: Histologic progression correlates with advancing age
- DOI:
10.1016/j.jaad.2021.01.028 - 发表时间:
2022-01-01 - 期刊:
- 影响因子:
- 作者:
Fritzlaine C. Roche;Andrew S. Fischer;Devin Williams;Temitayo Ogunleye;John T. Seykora;Susan C. Taylor - 通讯作者:
Susan C. Taylor
John T. Seykora的其他文献
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{{ truncateString('John T. Seykora', 18)}}的其他基金
Mechanisms regulating the early stages of UV-induced skin cancer
调节紫外线诱发皮肤癌早期阶段的机制
- 批准号:
10376752 - 财政年份:2018
- 资助金额:
$ 17.64万 - 项目类别:
Mechanisms regulating the early stages of UV-induced skin cancer
调节紫外线诱发皮肤癌早期阶段的机制
- 批准号:
9904163 - 财政年份:2018
- 资助金额:
$ 17.64万 - 项目类别:
The role of Fyn and Srcasm in UVB-induced cutaneous neoplasia
Fyn 和 Srcasm 在 UVB 诱导的皮肤肿瘤中的作用
- 批准号:
8513948 - 财政年份:2012
- 资助金额:
$ 17.64万 - 项目类别:
The role of Fyn and Srcasm in UVB-induced cutaneous neoplasia
Fyn 和 Srcasm 在 UVB 诱导的皮肤肿瘤中的作用
- 批准号:
8683129 - 财政年份:2012
- 资助金额:
$ 17.64万 - 项目类别:
The role of Fyn and Srcasm in UVB-induced cutaneous neoplasia
Fyn 和 Srcasm 在 UVB 诱导的皮肤肿瘤中的作用
- 批准号:
8392412 - 财政年份:2012
- 资助金额:
$ 17.64万 - 项目类别:
The role of Fyn and Srcasm in UVB-induced cutaneous neoplasia
Fyn 和 Srcasm 在 UVB 诱导的皮肤肿瘤中的作用
- 批准号:
8848791 - 财政年份:2012
- 资助金额:
$ 17.64万 - 项目类别:
The role of Fyn and Srcasm in UVB-induced cutaneous neoplasia
Fyn 和 Srcasm 在 UVB 诱导的皮肤肿瘤中的作用
- 批准号:
9110901 - 财政年份:2012
- 资助金额:
$ 17.64万 - 项目类别:
The role of srcasm in keratinocyte biology
srcasm 在角质形成细胞生物学中的作用
- 批准号:
7870731 - 财政年份:2009
- 资助金额:
$ 17.64万 - 项目类别:
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