Mathametical modeling of cell fate transitions regulated by ultra-feedbacks
Mathametical modeling of cell fate transitions regulated by ultra-feedbacks
批准号:
10457831
负责人:
Tian Hong
金额:
$20.0万
依托单位国家:
美国
项目类别:
财政年份:
2020
资助国家:
美国
项目状态:
已结题
起止时间:
2020-08-01 至 2024-07-31
关键词:
AddressAlgebraic GeometryApicalBindingBiologicalCell Fate ControlCell ProliferationCell modelCell physiologyCellsComplexDataDevelopmentDiseaseDisease ProgressionEmbryonic DevelopmentEnsureEnvironmentEpithelialEpithelial CellsFamilyFeedbackFibrosisGene Expression RegulationGene FamilyGenesGoalsInformation TheoryIntercellular JunctionsIntuitionMalignant NeoplasmsMathematicsMeasuresMesenchymalMethodsModelingNatural regenerationNatureNeoplasm MetastasisPathologicPathologic ProcessesPatternPhysiologicalPopulationProcessProliferatingPropertyRegenerative MedicineRegulationReportingResearchRoleSamplingSignal TransductionSourceStructureSystemTestingTissue EngineeringTransitional Epitheliumanalytical methodbasecancer therapycell motilitycell typecellular imagingdynamic systemepithelial to mesenchymal transitionexperimental studygene regulatory networkgenome editinginnovationinsightlive cell imagingmathematical analysismathematical methodsmathematical modelmulti-scale modelingpostnatal developmentpredictive modelingregenerative therapyresponsesimulationsuccesstheoriestooltranscription factortranscriptometranscriptomicstransdifferentiationtransmission processtumorwound healing
中文摘要
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英文摘要
Cell fate transition (conversion between cell types) is a fundamental process critical for development and
disease progression. Gene regulatory networks controlling cell fate transitions often involve positive
feedback loops. Recent data suggest that highly interconnected positive feedback loops (defined as ultra-
feedback circuit in this proposal) have additional functions, but the current understanding of these
networks is incomplete, partly due to the lack of theories and mathematical methods to analyze such
complex circuits. Epithelial-mesenchymal transition (EMT), a process in which rigid epithelial cells
convert to motile mesenchymal forms, is an example of cell fate transitions that are regulated by ultra-
feedback circuits. EMT occurs in both normal and pathological conditions such as metastasis. Recent
discoveries suggest two complex cellular properties that make EMT difficult to understand intuitively: the
formation of multiple intermediate EMT states and the partial reversibility of EMT. The functions of the
ultra-feedback circuits in regulating the two cellular properties are yet to be defined. The goal of the
proposed study is to gain deeper understanding of these properties of EMT by developing new methods,
models and theories to characterize the ultra-feedback circuits. We will combine real algebraic geometry,
stability analysis and numerical methods to identify stable steady states that arise from ultra-feedback
systems, and we will apply the method to analyze the EMT spectrum of cell types. We will quantify partially
reversible EMT with a new theoretical framework based on information theory and dynamical systems.
Theory driven simulations and experiments will be performed to examine how ultra-feedback circuits
control reversibility. We will characterize the roles of ultra-feedback circuits in cell motility and proliferation
during EMT using multiscale modeling and live-cell imaging. The proposal brings about new methods to
analyze a large, emerging family of dynamical systems containing a wide range of network structures, a
new theoretical framework for understanding information transmission and retainment, and a new
multiscale modeling framework for systems with complex state transitions and multiple sources of
stochasticity. The proposed study addresses fundamental questions about the interplay between two
important and emerging properties of EMT (its multistate nature and its restricted reversibility) with
mathematical innovations, and it will provide critical insights into gene regulations of cell fate transitions
during development and disease progression. The success of the project will lead to new quantitative
information of EMT and new concepts for better understanding EMT properties and for analyzing other cell
fate transitions involving ultra-feedback circuits.
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DOI:
10.1016/j.csbj.2020.11.017
发表时间:
2020
期刊:
Computational and structural biotechnology journal
影响因子:
6
作者:
[Liu Z, Shpak ED, Hong T]
通讯作者:
Hong T
DOI:
10.3390/cancers15051477
发表时间:
2023-02-25
期刊:
Cancers
影响因子:
5.2
作者:
[]
通讯作者:
DOI:
10.15252/msb.20209945
发表时间:
2021-04
期刊:
Molecular systems biology
影响因子:
9.9
作者:
[Li CJ, Liau ES, Lee YH, Huang YZ, Liu Z, Willems A, Garside V, McGlinn E, Chen JA, Hong T]
通讯作者:
Hong T
DOI:
10.1093/nargab/lqac072
发表时间:
2022-09
期刊:
NAR GENOMICS AND BIOINFORMATICS
影响因子:
4.6
作者:
[Panchy, Nicholas, Watanabe, Kazuhide, Takahashi, Masataka, Willems, Andrew, Hong, Tian]
通讯作者:
Hong, Tian
DOI:
10.1016/j.isci.2022.105224
发表时间:
2022-10-21
期刊:
ISCIENCE
影响因子:
5.8
作者:
[Nordick, Benjamin, Park, Mary Chae-Yeon, Quaranta, Vito, Hong, Tian]
通讯作者:
Hong, Tian
共 10 条
Modeling transcriptional and post-transcriptional systems for regulating non-genetic heterogeneity in mammalian cells
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批准号:10623648
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项目类别:
-
资助金额:$33.05万
-
财政年份:2023
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负责人:Tian Hong
-
依托单位:
Mathametical modeling of cell fate transitions regulated by ultra-feedbacks
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批准号:10221005
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项目类别:
-
资助金额:$20.0万
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财政年份:2020
-
负责人:Tian Hong
-
依托单位:
海外基金