2023 Germinal Stem Cell Biology GRC & GRS
2023 生殖干细胞生物学 GRC
基本信息
- 批准号:10609119
- 负责人:
- 金额:$ 1万
- 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:2023-02-01 至 2024-01-31
- 项目状态:已结题
- 来源:
- 关键词:AccelerationAgricultureAneuploidyAnimalsBioethicsBiologyBiotechnologyCell LineageCellsCellular biologyCollaborationsCommunicationCommunitiesDataDevelopmentDisabled PersonsDisciplineEmbryoEmbryologyEnvironmentEnvironmental ImpactEpigenetic ProcessEthicsFacultyFertilityFishesFosteringGenesGeneticGenomeGerm CellsGerm LinesGoalsGrowthHeterogeneityHourHumanIn VitroInfertilityInternationalLearningLightningLivestockMeiosisMentorsMetabolicMethodsModelingModificationMonkeysMusMutationPopulationPost-Transcriptional RegulationPostdoctoral FellowRNA metabolismRattusRecoveryRegulationReportingResearchResearch PersonnelScientistSecureSex ChromosomesSignal TransductionSomatic CellSpainSpecific qualifier valueStem Cell ResearchSystemTechniquesTimeUnderrepresented MinorityUnderrepresented PopulationsWomanX Inactivationcareercareer developmentcell typeclinically relevanteggembryo cellgraduate studentimprintinduced pluripotent stem cellinterestmeetingsmembernext generationnonhuman primateposterspreservationprofessorprogramsreproductive system disordersingle cell sequencingsperm cellstem cell biologystem cell populationstem cellssymposiumsynthetic biologytransmission processtumorverbal
项目摘要
GRC: GERMINAL STEM CELL BIOLOGY
Induction and Programming of the Germ Cell Lineage
Project Summary/Abstract
Germinal stem cells are the most potent known stem cell population, capable of giving rise to all embryonic and
extraembryonic cell types. Germ line stem cells were the first stem cell population recognized and, ever since,
have been the subject of intense research. They ultimately give rise to eggs and sperm and have the critical
responsibility of guarding the genome and transmitting it to the next generation. Researchers around the world
focus on understanding how germ line stem cells arise and how they are regulated at the genetic and epigenetic
levels to induce and maintain potency while safeguarding against the potential to differentiate as somatic cell
types or to form tumors. Lessons learned from this research have been instructive for all stem cell biology and
are crucial for understanding fertility and managing reproductive disorders. The pace of synthetic biology has
accelerated in recent years due to the advances in techniques such as single cell sequencing, epigenetic
analysis, and gene editing. New methods have allowed researchers to discover ways of efficiently inducing germ
line potency from a starting population of somatic cells and, more recently, of forming gonadal somatic lineages
from iPS cells that can potentially support germ cell development in mice, monkeys, and humans. These
discoveries advance the hope of producing gametes in vitro for applications in biomedicine such as infertility,
and applications in biotechnology such as species preservation and livestock management. This conference
will gather international scientists at the forefront of germ cell research with the goal of sharing the rapid
developments in the field among community members. This conference is focused on mammalian systems,
however vertebrate systems where recent advances have occurred are often included. We aim to make this
conference a forum for exchange among scientists interested in the basic biology of germinal stem cells and
those engaged in clinically relevant aspects of germ cell biology and fertility. Honoring the tradition of Gordon
Research Conferences, the meeting will be a venue to present unpublished data and cutting-edge advancements
in the field, followed by robust discussions. It will highlight emerging concepts and new research directions and
help establish collaborations across disciplines and across nations. Topics to be discussed include: specification
of the germ line, germ cell niches and signals, heterogeneity in the germ line, environment x epigenetic
programming in the germ line, metabolic regulation of germ cell development; in vitro development of germ cells
and fertility recovery; sex chromosomes and meiosis; mutation and aneuploidy in the germ line; RNA metabolism
and post-transcriptional control of germ cell development; and the bioethics of synthetic human embryology.
生殖干细胞生物学
生殖细胞谱系的诱导和编程
项目总结/摘要
胚胎干细胞是已知的最有效的干细胞群,能够产生所有的胚胎干细胞,
胚外细胞类型生殖系干细胞是第一个被认识到的干细胞群体,从那以后,
一直是研究的重点它们最终产生卵子和精子,
保护基因组并将其传递给下一代的责任。世界各地的研究人员
专注于了解生殖系干细胞是如何产生的,以及它们是如何在遗传和表观遗传方面受到调控的。
诱导和维持效力的水平,同时防止分化为体细胞的潜力
类型或形成肿瘤。从这项研究中吸取的教训对所有干细胞生物学和
对于了解生育能力和管理生殖疾病至关重要。合成生物学的发展速度
近年来,由于单细胞测序、表观遗传学和生物学等技术的进步,
分析和基因编辑。新方法使研究人员能够发现有效诱导细菌的方法,
从体细胞的起始群体,以及最近形成性腺体细胞谱系的细胞系潜能
从iPS细胞,可以潜在地支持小鼠,猴子和人类的生殖细胞发育。这些
这些发现推进了在体外产生配子用于生物医学如不孕症的希望,
以及生物技术的应用,如物种保护和牲畜管理。这次会议
将聚集生殖细胞研究前沿的国际科学家,
社区成员在该领域的发展。这次会议的重点是哺乳动物系统,
然而,经常包括最近取得进展的脊椎动物系统。我们的目标是让这个
会议是一个论坛,供对干细胞基础生物学感兴趣的科学家交流,
从事生殖细胞生物学和生育力临床相关方面的人员。尊重戈登的传统
研究会议,会议将是一个场地,提出未发表的数据和尖端的进步
在实地进行了讨论,随后进行了热烈的讨论。它将突出新兴概念和新的研究方向,
帮助建立跨学科和跨国家的合作。讨论的主题包括:规格
生殖细胞的生态位和信号,生殖细胞的异质性,环境x表观遗传
在生殖细胞系中编程,生殖细胞发育的代谢调节;生殖细胞的体外发育
性染色体和减数分裂;生殖系中的突变和非整倍体; RNA代谢
和生殖细胞发育的转录后控制;以及合成人类胚胎学的生物伦理学。
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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{{ truncateString('Blanche Capel', 18)}}的其他基金
DND1 Mediates Epigenetic Reprogramming During Cell Cycle Arrest In Male Germ Cells
DND1 在雄性生殖细胞细胞周期停滞期间介导表观遗传重编程
- 批准号:
10642896 - 财政年份:2021
- 资助金额:
$ 1万 - 项目类别:
DND1 Mediates Epigenetic Reprogramming During Cell Cycle Arrest In Male Germ Cells
DND1 在雄性生殖细胞细胞周期停滞期间介导表观遗传重编程
- 批准号:
10490349 - 财政年份:2021
- 资助金额:
$ 1万 - 项目类别:
DND1 Mediates Epigenetic Reprogramming During Cell Cycle Arrest In Male Germ Cells
DND1 在雄性生殖细胞细胞周期停滞期间介导表观遗传重编程
- 批准号:
10382834 - 财政年份:2021
- 资助金额:
$ 1万 - 项目类别:
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1
通过 RNA 结合蛋白 DND1 调节生殖细胞多能性
- 批准号:
8116405 - 财政年份:2010
- 资助金额:
$ 1万 - 项目类别:
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1
通过 RNA 结合蛋白 DND1 调节生殖细胞多能性
- 批准号:
8513346 - 财政年份:2010
- 资助金额:
$ 1万 - 项目类别:
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1
通过 RNA 结合蛋白 DND1 调节生殖细胞多能性
- 批准号:
8303437 - 财政年份:2010
- 资助金额:
$ 1万 - 项目类别:
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1
通过 RNA 结合蛋白 DND1 调节生殖细胞多能性
- 批准号:
7983700 - 财政年份:2010
- 资助金额:
$ 1万 - 项目类别:
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