Mesenchymal Stem Cells as Determinants of Tissue Aging
Mesenchymal Stem Cells as Determinants of Tissue Aging
批准号:
9164376
负责人:
MICHAEL WOSCZYNA
金额:
$10.08万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-09-30 至 2018-04-30
关键词:
AblationAdipocytesAgeAge-MonthsAgingAppearanceAreaAwardBiological AssayBiologyCell Culture SystemCellsCellular biologyCodeComputer SimulationCoupledDepositionDevelopmentDiseaseEnvironmentFatty acid glycerol estersFibrosisGenesGeneticGoalsHealthHistologyHomeostasisIn VitroInfiltrationInjuryIntramuscularKnowledgeLabelLeadLimb structureLongevityMediator of activation proteinMentorsMesenchymal Stem CellsMetabolic DiseasesMicroRNAsModelingMolecularMusMuscleMuscle functionNatural regenerationOrganismPathway interactionsPhasePrevalenceProcessRNAReporterResearchResearch PersonnelRoleSkeletal MuscleStem cellsTechnologyTestingTherapeutic InterventionTissuesTranscriptTransplantationUndifferentiatedUntranslated RNAWorkabstractingage relatedagedcell behaviordiphtheria toxin fragment Afunctional declinein vivointerstitialloss of functionmuscle regenerationnovelpreventprogenitorrecombinase-mediated cassette exchangeresearch studyskeletaltargeted treatmenttherapeutic targettissue processingtranscriptome sequencing
中文摘要
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英文摘要
Project Summary/Abstract
The appearance of fatty and fibrotic infiltration in aged skeletal muscle causes a decline in muscle function
and an increase in metabolic disorders. However, a means to mitigate this detrimental process remains
absent, as the cellular and molecular mechanisms that lead to the intramuscular accumulation of these
adverse atypical tissues are not well understood. Recently identified mesenchymal stem cells (MSCs) that
occupy the interstitial space of skeletal muscle (interstitial MSCs, iMSCs) have been postulated as the
foremost cellular mediators of adiposis and fibrosis. In young tissue iMSCs do not covert to these fates, but
instead, remain as progenitors and are assumed to support the processes of tissue homeostasis and
regeneration. We hypothesize that the fate of iMSCs determine their impact on skeletal muscle and with age,
iMSCs become the adipocytes and fibrocytes that negatively impact the organism as a whole. In the studies of
this proposal, we will define the role of iMSCs in intramuscular fatty and fibrotic infiltration by genetically
targeting the cell in vivo and examining its developmental potential in models of aged skeletal muscle (Aim 1).
We will also determine the necessity of iMSCs in skeletal muscle homeostasis and regeneration in young and
aged milieus by specifically depleting iMSCs in vivo and then examining these activities (Aim 2). Finally, we will
define the molecular pathways of iMSC fate progression by modeling this process in vitro and using advanced
RNA sequencing technologies to reveal non-coding and coding RNA species that can functionally modulate
cell fate determination (Aim 3). Our overarching goal is to elucidate the impact iMSC fate has on skeletal
muscle and to leverage these findings to develop therapeutic targets to mitigate age-related skeletal muscle
decline.
The candidate, Dr. Michael Wosczyna, has extensive expertise in experimental progenitor cell biology and
has spent more than a decade studying stem cell-related disorders. During the mentoring phase of this award,
Dr. Wosczyna aims to advance his knowledge in age-related stem cell decline and in massively parallel
technologies used for uncovering genetic pathways of fate determination. Dr. Wosczyna's mentor and co-
mentor, Dr. Thomas Rando and Dr. Judith Campisi, respectively, have comprehensive expertise in these
areas. They will provide an enriching environment for Dr. Wosczyna to develop as a prominent independent
investigator in aging research.
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Mesenchymal Stem Cells as Determinants of Tissue Aging
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批准号:10359756
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项目类别:
-
资助金额:$24.53万
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财政年份:2016
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负责人:MICHAEL WOSCZYNA
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依托单位:
Mesenchymal Stem Cells as Determinants of Tissue Aging
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批准号:10160729
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项目类别:
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资助金额:$24.72万
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财政年份:2016
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负责人:MICHAEL WOSCZYNA
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依托单位:
国内基金
海外基金
支链氨基酸代谢紊乱调控“Adipocytes - Macrophages Crosstalk”诱发2型糖尿病脂肪组织功能和结构障碍的作用及机制
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批准号:81970721
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项目类别:面上项目
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资助金额:55.0万元
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批准年份:2019
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负责人:陶凌
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依托单位: