Role in Myopia Development of Retinal Pigment Epithelium - A New Therapeutic Targ
视网膜色素上皮在近视发展中的作用——一种新的治疗目标
基本信息
- 批准号:8915182
- 负责人:
- 金额:$ 14.97万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2013
- 资助国家:美国
- 起止时间:2013-09-30 至 2016-08-31
- 项目状态:已结题
- 来源:
- 关键词:AcademiaAffectAnimal ModelAnimalsApicalApomorphineAwardBloodBone Morphogenetic Protein GeneBone Morphogenetic ProteinsCaliforniaCell Culture TechniquesCell Differentiation processCellsCellular biologyChoroidClinicalCloningCommunitiesDataDevelopmentDevelopmental BiologyDisciplineDiseaseDoctor of PhilosophyDopamineDopamine AgonistsElectrophysiology (science)ElectroporationElectroretinographyEmbryonic DevelopmentEnvironmentEnzyme-Linked Immunosorbent AssayExtracellular MatrixEyeEye diseasesFamilyFrequenciesFundingGene ExpressionGenesGoalsGrantGrowthGrowth FactorHarvestHealthHumanImageImmunohistochemistryIn VitroIndividualInvestigationJournalsK-Series Research Career ProgramsKnowledgeMeasurementMeasuresMediatingMedicineMentorsMentorshipModelingMolecular BiologyMorphogenesisMyopiaOphthalmologyOptic NerveOptical Coherence TomographyOpticsOutcomePaperPhysiologyPlayPopulationPositioning AttributePreparationPrevalenceProductionProductivityProtein FamilyProtein SecretionPublicationsRefractive ErrorsRegulationResearchResearch PersonnelResearch ProposalsRetinaRetinalRiskRoleSan FranciscoScanningScientistSenior ScientistSeveritiesSignal TransductionStructure of retinal pigment epitheliumTechniquesTechnologyTestingTherapeutic InterventionTherapeutic StudiesTimeTissuesTrainingTranslational ResearchUltrasonographyUnited States National Institutes of HealthUniversitiesVirusWestern Blottingage groupbonebone morphogenetic protein 2careercareer developmentdifferential expressioneconomic implicationexperiencefetalfollow-upgene therapyimmunocytochemistryin vitro Modelin vivoknock-downlensmembernew therapeutic targetnovelnovel therapeuticspreventprofessorprogramsprotein expressionreceptorresearch studyresponseskillssocial implicationsubretinal injectionvision science
项目摘要
DESCRIPTION (provided by applicant): The Mentored Clinical Scientist Research Career Development Award (K08) candidate, Yan Zhang, earned her clinical degrees in Medicine and Ophthalmology, and she is currently pursuing her Ph.D. degree in the Vision Science Program at University of California, Berkeley, which will be completed in the Spring 2013. She has already one publication in a high profile journal from the latter research, with 2 more papers soon to be submitted, demonstrating both good productivity and research drive. As the next step towards a career as an independent clinician scientist in academia, Dr. Zhang is applying for a K08 career award to obtain advanced training - to further expand her scientific knowledge and biomedical technical skills through investigations into the roles of retinal pigment epithelium (RPE) and bone morphogenetic proteins (BMPs) in eye growth regulation and myopia development, with the RPE targeted in related exploratory studies of gene therapy for myopia treatment. Over the course of her studies to-date, Dr. Zhang has received broad training in many of the disciplines required for successfully executing her proposed project. She proposed to cover remaining deficiencies with additional coursework and hands-on training during the 5-year training period of the K award for which she is applying. Thus at the end of this 5-year career development award Dr. Zhang should be well prepared for a career as an independent researcher, successfully competing for research funds. The proposed study will be conducted primarily under the mentorship of Dr. Christine Wildsoet, who is a well- known leading scientist in the field of myopia and eye growth regulation. Myopia, or nearsightedness, is one of most common refractive errors in humans and significantly contributes to the global burden of eye disease. It is the product of eyes growing excessively long. The prevalence and the severity of myopia have risen worldwide during the past several decades, stimulating increased research into the underlying mechanisms, an essential step in developing effective anti-myopia therapies. Previous studies have suggested that early eye growth regulation is largely localized to eye itself. The RPE is known to be a component of the blood-retina barrier, with critical roles in maintaining normal retinal and choroidal functions. Recent research findings, mostly from the Wildsoet lab and much of it belongs to Dr. Zhang, suggest that it also plays an essential role in the regulation of eye growth. The proposal focuses on the role of RPE in myopia development and as a potential target for myopia therapy, with 3 specific aims: (1) to investigate the role of RPE-derived bone morphogenetic proteins (BMPs) in eye growth regulation; (2) to investigate the effects of dopamine (DA) on RPE-BMP expression and secretion; (3) to investigate over-expression of BMPs in RPE as a potential gene therapy for myopia. Complementary experiments include in vivo animal studies, using the chick as an myopia model, and in vitro cell culture studies, using human fetal (hf) RPE as a model, exploiting Dr. Zhang's experience with both models. In vivo structural and functional measurements will use advanced technologies, including high frequency A-scan ultrasonography, spectral domain optical coherence tomography (SD-OCT) and electroretinography (ERG). A variety of molecular and cell biology techniques will also be used including cloning, real-time PCR, Western blot, ELISA, and immunohistochemistry. Techniques most commonly encountered in ocular gene therapy research, including electroporation and subretinal injection, will also be employed. The proposed research will be conducted under the co-mentorship of Dr. Jeanette Hyer from UC San Francisco, who is an expert in developmental biology, with a focus on chick embryogenesis. Three senior scientists have also agreed to serve as consultants on her project: Professor Lawrence Rizzolo (Yale University) and Dr. Sheldon Miller (NEI/NIH), who are experts in RPE physiology and electrophysiology, and Professor Kunxin Luo (UC Berkeley), whose research focus is the TGF-� family including BMPs and their roles in cell differentiation, tissue morphogenesis, and extracellular matrix production. UC Berkeley and UC San Francisco offer world-class research environments and support for the preparation and training of young scientists for independent research careers.
描述(由申请人提供):导师临床科学家研究职业发展奖(K08)候选人张艳获得了医学和眼科临床学位,目前正在大学视觉科学项目攻读博士学位。加利福尼亚州伯克利分校的研究将于 2013 年春季完成。她已经在一家备受瞩目的期刊上发表了一篇关于后者研究的论文,并且即将提交另外 2 篇论文,展示了良好的生产力和研究动力。作为学术界独立临床科学家职业生涯的下一步,张博士正在申请 K08 职业奖以进行高级培训 - 通过研究视网膜色素上皮 (RPE) 的作用,进一步扩展她的科学知识和生物医学技术技能)和骨形态发生蛋白(BMP)在眼睛生长调节和近视发展中的作用,其中 RPE 是近视治疗基因疗法的相关探索性研究的目标。张博士接受了成功执行其拟议项目所需的许多学科的广泛培训,她建议在她申请的 K 奖的 5 年培训期间通过额外的课程作业和实践培训来弥补剩余的缺陷。因此,在这个 5 年职业发展奖结束时,张博士应该为作为一名独立研究人员的职业生涯做好充分准备,成功竞争研究基金。拟议的研究将主要在 Christine Wildsoet 博士的指导下进行。是一位著名的领先科学家近视和眼睛生长调节领域 近视或近视是人类最常见的屈光不正之一,它是眼睛生长过长的患病率和严重程度的结果。近几十年来,近视在全球范围内有所增加,这刺激了对其潜在机制的研究,这是开发有效的抗近视疗法的重要一步,众所周知,早期眼睛生长调节主要局限于眼睛本身。是血视网膜屏障的组成部分,在维持正常视网膜和脉络膜功能方面发挥着关键作用。最近的研究结果(大部分来自 Wildsoet 实验室,其中大部分属于张博士)表明,它在维持正常视网膜和脉络膜功能方面也发挥着重要作用。该提案重点关注 RPE 在近视发展中的作用以及作为近视治疗的潜在靶点,有 3 个具体目标:(1)研究 RPE 衍生的骨形态发生蛋白(BMP)在近视发展中的作用。眼睛生长调节;(2) 研究多巴胺 (DA) 对 RPE-BMP 表达和分泌的影响;(3) 研究 RPE 中 BMP 的过度表达作为近视的潜在基因治疗。使用小鸡作为近视模型的研究,以及使用人类胎儿(HF)RPE作为模型的体外细胞培养研究,利用张博士在这两种模型方面的经验,将使用先进的体内结构和功能测量。技术,包括高频 A 扫描超声检查、频域光学相干断层扫描 (SD-OCT) 和视网膜电图检查 (ERG) 还将使用各种分子和细胞生物学技术,包括克隆、实时 PCR、蛋白质印迹、ELISA。和免疫组织化学在眼部基因治疗研究中最常见的技术,包括电穿孔和视网膜下注射,也将在该项目下进行。来自加州大学旧金山分校的 Jeanette Hyer 博士是发育生物学专家,专注于鸡胚胎发生,三位资深科学家也同意担任她的项目顾问:Lawrence Rizzolo 教授(耶鲁大学)和Sheldon Miller 博士(NEI/NIH)是 RPE 生理学和电生理学专家,Kunxin Luo 教授(加州大学伯克利分校)的研究重点是 TGF-β 家族,包括 BMP 及其在细胞分化中的作用,加州大学伯克利分校和加州大学旧金山分校为年轻科学家的独立研究生涯的准备和培训提供世界一流的研究环境和支持。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Yan Zhang其他文献
Designing a multi-species spatially explicit nature reserve network construction framework based on extinction probability: A case study of Wuyishan city
基于灭绝概率的多物种空间清晰自然保护区网络构建框架设计——以武夷山市为例
- DOI:
- 发表时间:
2014 - 期刊:
- 影响因子:0
- 作者:
Gengyuan Liu;Zhifeng Yang;Bin Chen;Shan Gao;Meirong Su;Yan Zhang - 通讯作者:
Yan Zhang
Yan Zhang的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Yan Zhang', 18)}}的其他基金
The stage-specific regulation of ameloblastin and enamelin by the distinct nuclear factors
不同核因子对成釉素和釉质的阶段特异性调节
- 批准号:
10804126 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别:
High Urinary Phosphate Induces TLR4-mediated Inflammation and Cystogenesis in Polycystic Kidney Disease
高尿磷酸盐诱导多囊肾病中 TLR4 介导的炎症和囊肿发生
- 批准号:
10730615 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别:
The stage-specific regulation of ameloblastin and enamelin by the distinct nuclear factors
不同核因子对成釉素和釉质的阶段特异性调节
- 批准号:
10645781 - 财政年份:2022
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10454868 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10227166 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10026656 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10664972 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10664972 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Generation of DNA memory by bacterial CRISPR-Cas9 systems
通过细菌 CRISPR-Cas9 系统生成 DNA 记忆
- 批准号:
10792662 - 财政年份:2020
- 资助金额:
$ 14.97万 - 项目类别:
Investigating the Role of BACE2 in Melanocyte Development and Melanoma Progression
研究 BACE2 在黑色素细胞发育和黑色素瘤进展中的作用
- 批准号:
9814738 - 财政年份:2019
- 资助金额:
$ 14.97万 - 项目类别:
相似国自然基金
肾—骨应答调控骨骼VDR/RXR对糖尿病肾病动物模型FGF23分泌的影响及中药的干预作用
- 批准号:82074395
- 批准年份:2020
- 资助金额:55 万元
- 项目类别:面上项目
基于细胞自噬调控的苦参碱对多囊肾小鼠动物模型肾囊肿形成的影响和机制研究
- 批准号:
- 批准年份:2019
- 资助金额:33 万元
- 项目类别:地区科学基金项目
靶向诱导merlin/p53协同性亚细胞穿梭对听神经瘤在体生长的影响
- 批准号:81800898
- 批准年份:2018
- 资助金额:21.0 万元
- 项目类别:青年科学基金项目
NRSF表达水平对抑郁模型小鼠行为的影响及其分子机制研究
- 批准号:81801333
- 批准年份:2018
- 资助金额:21.0 万元
- 项目类别:青年科学基金项目
伪狂犬病病毒激活三叉神经节细胞对其NF-кB和PI3K/Akt信号转导通路影响的分子机制研究
- 批准号:31860716
- 批准年份:2018
- 资助金额:39.0 万元
- 项目类别:地区科学基金项目
相似海外基金
Targeting microglial cell iron-handling in Alzheimer’s Disease
靶向阿尔茨海默病中的小胶质细胞铁处理
- 批准号:
10603992 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别:
Hyperpolarized 13C metabolic imaging in an endovascular swine model of ischemic stroke
缺血性中风血管内猪模型的超极化 13C 代谢成像
- 批准号:
10726555 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别:
The CRISPR Vision Program: Nonviral Genome Editing Platforms to Treat Inherited Retinal Channelopathies
CRISPR 视觉计划:治疗遗传性视网膜通道病的非病毒基因组编辑平台
- 批准号:
10668161 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别:
Development and Production of Standardized Reference Diets for Zebrafish Research
斑马鱼研究标准化参考饲料的开发和生产
- 批准号:
10823702 - 财政年份:2023
- 资助金额:
$ 14.97万 - 项目类别: