Imaging spatial transcriptome at single cell resolution to study eye regeneration in old age
以单细胞分辨率对空间转录组进行成像以研究老年眼再生
基本信息
- 批准号:10785595
- 负责人:
- 金额:$ 19.5万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-09-30 至 2026-05-31
- 项目状态:未结题
- 来源:
- 关键词:AgeAge related macular degenerationAgingAnimal ModelAnimalsArchitectureAtlasesBody partCell CommunicationCellsCollaborationsDataData SetDevelopmentDiseaseElderlyEyeFresh WaterGene ExpressionGenesGoalsHeadImageImpairmentKnowledgeLaboratory cultureLearningMethodsMolecularNatural regenerationOutputPathway interactionsPatientsPatternPersonsPhenotypePigmentsPlanariansPlatyhelminthsProcessProductionQuality of lifeRegenerative MedicineRegenerative capacityRegulationRejuvenationReportingResearchResolutionSignal TransductionSlideTechnologyTherapeuticTissuesWorkadult stem cellage relatedagedcell typedifferential expressionempowermentexperimental studyeye regenerationfightinghuman old age (65+)improvedmolecular dynamicsnext generationolder patientprogenitorregenerativerepairedsingle cell mRNA sequencingstem cell biologystem cell functionstem cell technologystem cellstheoriestissue regenerationtooltranscriptometranscriptomics
项目摘要
ABSTRACT
To cure age-related diseases is of critical importance for the life quality of elderly people. One promising strategy
is to slow down aging or reverse aging with regenerative medicine. However, the regenerative capacity of stem
cells and their supportive microenvironments are drastically impaired in old age. Hence, to rejuvenate functions
of aged adult stem cells and their microenvironments or to maintain the youthful functions of adult stem cells in
old age are critical research directions to empower regenerative medicine to fight age-associated diseases. Here,
we propose to use a cutting-edge spatial transcriptomics method, Seq-Scope, to comprehensively examine the
aging, regeneration and rejuvenation of eye progenitor cells and their niche cells in the sexual planarians, a
champion of tissue regeneration. We aim to determine the molecular pathways that facilitate regeneration and
rejuvenation in old age. The proposed experiments will define datasets of fundamental importance in the
identification of niche cells and changes in aging and regeneration that will fuel long-term mechanistic studies.
摘要
老年病的治疗对老年人的生活质量至关重要。一个很有前途的策略
就是用再生医学来减缓衰老或者逆转衰老。然而,茎的再生能力
细胞及其支持微环境在老年时严重受损。因此,为了恢复功能,
或维持成体干细胞的年轻功能,
老年是关键的研究方向,使再生医学能够对抗与年龄相关的疾病。在这里,
我们建议使用尖端的空间转录组学方法Seq-Scope来全面检查
性真涡虫眼祖细胞及其生态位细胞的衰老、再生和复壮,
组织再生的冠军我们的目标是确定促进再生的分子途径,
在年老时恢复活力。拟议的实验将定义数据集的根本重要性,
识别小生境细胞以及老化和再生的变化,这将推动长期的机制研究。
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 }}
Longhua Guo其他文献
Longhua Guo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 }}
相似海外基金
I(eye)-SCREEN: A real-world AI-based infrastructure for screening and prediction of progression in age-related macular degeneration (AMD) providing accessible shared care
I(eye)-SCREEN:基于人工智能的现实基础设施,用于筛查和预测年龄相关性黄斑变性 (AMD) 的进展,提供可及的共享护理
- 批准号:
10102692 - 财政年份:2024
- 资助金额:
$ 19.5万 - 项目类别:
EU-Funded
Inhibiting Neovascularization and Subretinal Fibrosis in Neovascular Age-Related Macular Degeneration
抑制新生血管性年龄相关性黄斑变性的新生血管形成和视网膜下纤维化
- 批准号:
10639785 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Inhibition of melanogenesis in retinal pigment epithelium, a contributing factor in age-related macular degeneration
抑制视网膜色素上皮中的黑色素生成,这是年龄相关性黄斑变性的一个促成因素
- 批准号:
23K09052 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Deciphering the role of osteopontin in the aging eye and age-related macular degeneration
破译骨桥蛋白在眼睛老化和年龄相关性黄斑变性中的作用
- 批准号:
10679287 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Evaluation of New Anti-inflammatory Treatments for Age-Related Macular Degeneration
年龄相关性黄斑变性的新型抗炎治疗方法的评价
- 批准号:
10642988 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Progression of Early Atrophic Lesions in Age-related Macular degeneration
年龄相关性黄斑变性早期萎缩性病变的进展
- 批准号:
10635325 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Cellular and molecular mechanisms of AIM2 and NLRP3 inflammasome activation in age-related macular degeneration
年龄相关性黄斑变性中 AIM2 和 NLRP3 炎症小体激活的细胞和分子机制
- 批准号:
10584110 - 财政年份:2023
- 资助金额:
$ 19.5万 - 项目类别:
Elucidation of roles of mast cells and macrophages in the pathogenesis of age-related macular degeneration
阐明肥大细胞和巨噬细胞在年龄相关性黄斑变性发病机制中的作用
- 批准号:
22H03243 - 财政年份:2022
- 资助金额:
$ 19.5万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
AMD Mitochondria Modulate Expression of microRNA 135b-5p and 148a-3p in RPE Cybrids: Implications for Age-related Macular Degeneration
AMD 线粒体调节 RPE Cybrids 中 microRNA 135b-5p 和 148a-3p 的表达:对年龄相关性黄斑变性的影响
- 批准号:
10433610 - 财政年份:2022
- 资助金额:
$ 19.5万 - 项目类别:
Targeting the inflammatory response in age-related macular degeneration
针对年龄相关性黄斑变性的炎症反应
- 批准号:
10504138 - 财政年份:2022
- 资助金额:
$ 19.5万 - 项目类别:














{{item.name}}会员




