Transcriptional regulation of skin stem cells and their niche
皮肤干细胞及其生态位的转录调控
基本信息
- 批准号:10261535
- 负责人:
- 金额:$ 34.14万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2017
- 资助国家:美国
- 起止时间:2017-07-28 至 2023-04-30
- 项目状态:已结题
- 来源:
- 关键词:ATAC-seqAdultAffectBiologyCell AdhesionCell CompartmentationCell MaintenanceCell divisionCellsChromatinDNA Sequence AlterationDNA biosynthesisEnhancersFOXC1 geneGene ExpressionGenerationsGenesGenomicsGoalsHairHair follicle structureHomeostasisIndividualKnock-outKnockout MiceKnowledgeLeadLifeMaintenanceMediatingModelingMolecularMusOrganismPhasePlayPropertyRegenerative MedicineRegulationResearchResearch PersonnelRoleSignal TransductionSkinSystemTimeTissuesTranscriptional Regulationadult stem cellcell motilitygenomic toolshair regenerationin vivoinnovationinsightmigrationmouse modelresponseself-renewalstem cell biologystem cell functionstem cell populationstem cell self renewalstem cellstissue regenerationtranscription factortranscriptometumorigenesiswound healing
项目摘要
Project Summary:
The overarching goal of the proposed research is to understand how skin stem cells maintain
their identity when responding to cell intrinsic and extrinsic signals for self-renewal or
differentiation. Self-renewal of stem cells is achieved by either symmetrical or asymmetrical cell
division, through which new generations of stem cells are produced to replenish the stem cell
population. However, DNA replication and cell division of adult stem cells can also lead to
generation and accumulation of DNA mutations that compromise stem cell function and, in
some cases, tumorigenesis. In the skin, hair follicle stem cells acquire quiescence to minimize
cell turnover and division. However, it remains poorly understood how these stem cells
transition between self-renewing and quiescent phases and the requirement of quiescence for
long-term maintenance of stem cells. These questions have challenged investigators, because
these self-renewing and quiescent stem cells are rare and usually heterogeneous in most adult
tissues, making their isolation and characterization difficulty. In the skin of early adult mice, hair
follicle stem cells are highly synchronized for self-renewal and quiescence. This property makes
hair follicle stem cells an ideal system to investigate this fundamental question in stem cell
biology. Recently, we have identified a transcription factor, Foxc1, induced in self-renewing but
not quiescent hair follicle stem cells and their niche to reinforce quiescence. This finding
uncovers an adaptive response of quiescent stem cells to stem cell activation during self-
renewal and illuminates a path to further investigate mechanisms that control cellular state
transitions in adult stem cells. In this proposal, we will utilize our innovative genomic tools and
mouse models to understand adaptive control of stem cell quiescence and self-renewal
mediated by transcription factors. We will first determine how multiple transcription factors
regulate stem cell quiescence by coordinating transcriptional control of common and unique
targets. We will determine the requirement of quiescence for long-term maintenance of hair
follicle stem cells (Aim 1). We will then investigate the differences in open chromatin between
self-renewing and quiescent stem cells. We will examine how the BMP signaling is controlled by
transcription factors (Aim 2). Finally, we will investigate the mechanism of club hair anchorage
mediated by transcription factors (Aim 3). The knowledge gained from these studies will
enhance our understanding of quiescence control in hair follicle stem cells.
项目概要:
这项研究的首要目标是了解皮肤干细胞是如何维持
当响应细胞内在和外在信号进行自我更新时,
分化干细胞的自我更新是通过对称或不对称的细胞
分裂,通过分裂产生新一代的干细胞以补充干细胞
人口然而,成体干细胞的DNA复制和细胞分裂也可导致
DNA突变的产生和积累损害干细胞功能,
有些情况下是肿瘤形成在皮肤中,毛囊干细胞获得静止,
细胞更新和分裂。然而,人们对这些干细胞是如何产生的仍然知之甚少。
自我更新期和静止期之间的过渡以及静止期的要求
干细胞的长期维持。这些问题对调查人员提出了挑战,因为
这些自我更新和静止的干细胞在大多数成年人中是罕见的,
组织,使其分离和表征困难。在早期成年小鼠的皮肤中,
毛囊干细胞高度同步地进行自我更新和静止。此属性使
毛囊干细胞是研究干细胞中这一基本问题的理想系统
生物学最近,我们已经确定了一个转录因子,Foxc1,诱导自我更新,但
而不是静止的毛囊干细胞和它们的小生境来加强静止。这一发现
揭示了静止干细胞在自我激活过程中对干细胞激活的适应性反应。
更新,并阐明了进一步研究控制细胞状态的机制的途径
成体干细胞的转变在这项提案中,我们将利用我们创新的基因组工具,
了解干细胞静止和自我更新的适应性控制的小鼠模型
由转录因子介导。我们将首先确定多种转录因子
调节干细胞静止通过协调转录控制的共同和独特的
目标的我们将确定长期保持头发静止的要求
卵泡干细胞(Aim 1)。然后,我们将研究开放染色质的差异,
自我更新和静止的干细胞。我们将研究BMP信号是如何被
转录因子(Aim 2)。最后,我们将探讨棒毛锚定的机制
由转录因子介导(Aim 3)。从这些研究中获得的知识将
增强我们对毛囊干细胞静止控制的理解。
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 }}
Rui Yi其他文献
Rui Yi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('Rui Yi', 18)}}的其他基金
Investigate MOF regulated epigenetic mechanisms of skin development
研究 MOF 调节皮肤发育的表观遗传机制
- 批准号:
10467552 - 财政年份:2022
- 资助金额:
$ 34.14万 - 项目类别:
Modeling p63-associated human birth defects with systems developmental biology approaches
利用系统发育生物学方法对 p63 相关人类出生缺陷进行建模
- 批准号:
10539094 - 财政年份:2022
- 资助金额:
$ 34.14万 - 项目类别:
Modeling p63-associated human birth defects with systems developmental biology approaches
利用系统发育生物学方法对 p63 相关人类出生缺陷进行建模
- 批准号:
10705852 - 财政年份:2022
- 资助金额:
$ 34.14万 - 项目类别:
Investigate MOF regulated epigenetic mechanisms of skin development
研究 MOF 调节皮肤发育的表观遗传机制
- 批准号:
10632030 - 财政年份:2022
- 资助金额:
$ 34.14万 - 项目类别:
Transcriptional regulation of skin stem cells and their niche
皮肤干细胞及其生态位的转录调控
- 批准号:
10682202 - 财政年份:2017
- 资助金额:
$ 34.14万 - 项目类别:
Transcriptional regulation of skin stem cells and their niche
皮肤干细胞及其生态位的转录调控
- 批准号:
10252398 - 财政年份:2017
- 资助金额:
$ 34.14万 - 项目类别:
Genetic Analysis of MicroRNA Functions in Skin Stem Cells in Vivo
体内皮肤干细胞 MicroRNA 功能的遗传分析
- 批准号:
9285727 - 财政年份:2014
- 资助金额:
$ 34.14万 - 项目类别:
Genetic Analysis of MicroRNA Functions in Skin Stem Cells In Vivo
体内皮肤干细胞 MicroRNA 功能的遗传分析
- 批准号:
9913969 - 财政年份:2014
- 资助金额:
$ 34.14万 - 项目类别:
Genetic Analysis of MicroRNA Functions in Skin Stem Cells in Vivo
体内皮肤干细胞 MicroRNA 功能的遗传分析
- 批准号:
8762616 - 财政年份:2014
- 资助金额:
$ 34.14万 - 项目类别:
Genetic Analysis of MicroRNA Functions in Skin Stem Cells In Vivo
体内皮肤干细胞 MicroRNA 功能的遗传分析
- 批准号:
10544018 - 财政年份:2014
- 资助金额:
$ 34.14万 - 项目类别:
相似海外基金
Co-designing a lifestyle, stop-vaping intervention for ex-smoking, adult vapers (CLOVER study)
为戒烟的成年电子烟使用者共同设计生活方式、戒烟干预措施(CLOVER 研究)
- 批准号:
MR/Z503605/1 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Research Grant
Early Life Antecedents Predicting Adult Daily Affective Reactivity to Stress
早期生活经历预测成人对压力的日常情感反应
- 批准号:
2336167 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Standard Grant
RAPID: Affective Mechanisms of Adjustment in Diverse Emerging Adult Student Communities Before, During, and Beyond the COVID-19 Pandemic
RAPID:COVID-19 大流行之前、期间和之后不同新兴成人学生社区的情感调整机制
- 批准号:
2402691 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Standard Grant
Migrant Youth and the Sociolegal Construction of Child and Adult Categories
流动青年与儿童和成人类别的社会法律建构
- 批准号:
2341428 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Standard Grant
Elucidation of Adult Newt Cells Regulating the ZRS enhancer during Limb Regeneration
阐明成体蝾螈细胞在肢体再生过程中调节 ZRS 增强子
- 批准号:
24K12150 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Understanding how platelets mediate new neuron formation in the adult brain
了解血小板如何介导成人大脑中新神经元的形成
- 批准号:
DE240100561 - 财政年份:2024
- 资助金额:
$ 34.14万 - 项目类别:
Discovery Early Career Researcher Award
Laboratory testing and development of a new adult ankle splint
新型成人踝关节夹板的实验室测试和开发
- 批准号:
10065645 - 财政年份:2023
- 资助金额:
$ 34.14万 - 项目类别:
Collaborative R&D
Usefulness of a question prompt sheet for onco-fertility in adolescent and young adult patients under 25 years old.
问题提示表对于 25 岁以下青少年和年轻成年患者的肿瘤生育力的有用性。
- 批准号:
23K09542 - 财政年份:2023
- 资助金额:
$ 34.14万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Identification of new specific molecules associated with right ventricular dysfunction in adult patients with congenital heart disease
鉴定与成年先天性心脏病患者右心室功能障碍相关的新特异性分子
- 批准号:
23K07552 - 财政年份:2023
- 资助金额:
$ 34.14万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Issue identifications and model developments in transitional care for patients with adult congenital heart disease.
成人先天性心脏病患者过渡护理的问题识别和模型开发。
- 批准号:
23K07559 - 财政年份:2023
- 资助金额:
$ 34.14万 - 项目类别:
Grant-in-Aid for Scientific Research (C)