Developmental control of cell polarity in vertebrate embryos.
Developmental control of cell polarity in vertebrate embryos.
批准号:
7876837
负责人:
John B Wallingford
金额:
$26.41万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-06-19 至 2012-05-31
关键词:
AffectApicalBindingCell PolarityCell membraneCell physiologyCellsCellular biologyCentrosomeChimeric ProteinsCiliaCilium MicrotubuleClathrin AdaptorsComplexCongenital AbnormalityCystic Kidney DiseasesCytoskeletonDNA Sequence RearrangementDefectDevelopmentDevelopmental ProcessDockingEmbryoEmbryonic DevelopmentEndosomesEpithelial CellsEventExocytosisFRZB proteinGoalsGuanosine Triphosphate PhosphohydrolasesHumanHuman PathologyImageImmigrationInfertilityKidneyLightLinkMediatingMembraneMicrotubulesMolecularMorphogenesisMovementNervous System PhysiologyNeural Tube ClosureNeuraxisObesityPathologyPathway interactionsPatternPlayPositioning AttributeProteinsRecyclingReproductive systemRoleSignal TransductionSitus InversusSorting - Cell MovementSpeedSpinal DysraphismSyndromeTestingTimeTissuesTranscription Factor AP-1VertebratesVesicleWorkXenopusbasecell behaviorcell motilitycilium biogenesisfluid flowin vivointercalationkinetosomeprotein functionresearch studytrafficking
中文摘要
我们实验室的一个长期目标是了解细胞极性的分子基础,
脊椎动物胚胎的组织形态发生。我们在这里的重点是平面细胞极性(PCP)信号级联,一种分子机制,既管理纤毛的形成和细胞运动称为收敛延伸。纤毛是基于微管的细胞突起,在广泛的人类病理学中具有重要作用。例如,由纤毛细胞产生的定向流体流动对于
神经系统、肾脏、生殖系统和呼吸道的功能。这种“纤毛病”包括囊性肾病、肥胖综合征、不育、位置异常和中枢神经系统的形态缺陷。包括人类在内的脊椎动物的神经管闭合需要会聚延伸细胞运动。这项建议将研究PCP蛋白,弗里茨,在纤毛发生和会聚延伸的作用。在纤毛发生过程中,我们将问弗里茨在微管的多聚谷氨酰化和隔蛋白细胞骨架的组织中起什么作用。在会聚延伸过程中,我们将询问Fritz如何控制细胞行为,包括膜扩散活性和中心体定位。总之,这些实验将帮助我们了解PCP信号如何影响会聚延伸和纤毛发生等不同的细胞过程。
英文摘要
A long-term goal of our lab is to understand the molecular basis of cell polarity and
tissue morphogenesis in vertebrate embryos. Our focus here is on the Planar Cell Polarity (PCP) signaling cascade, a molecular mechanism that governs both the formation of cilia and cell movements called convergent extension. Cilia are microtubule-based projections of the cell with important roles in a wide range of human pathologies. For example, the directed fluid flow generated by ciliated cells is crucial for
the function of the nervous system, the kidney, the reproductive systems, and the airway. Such “ciliopathies” include cystic kidney diseases, obesity syndromes, infertility, situs abnormalities, and morphological defects on the central nervous system. Convergent extension cell movements are required for neural tube closure in vertebrates, including humans. This proposal will examine the role of the PCP protein, Fritz, in ciliogenesis and convergent extension. During ciliogenesis, we will ask what role Fritz plays in polyglutamylation of microtubules and in the organization of the septin cytoskeleton. During convergent extension, we will ask how Fritz controls cell behaviors, including membrane protrusive activity and centrosomal positioning. Together, these experiments will help us to understand how PCP signaling influences such diverse cellular processes as convergent extension and ciliogenesis.
期刊论文(1)
专著(0)
科研奖励(0)
会议论文
PCP-dependent transcellular regulation of actomyosin oscillation facilitates convergent extension of vertebrate tissue.
肌动球蛋白振荡的 PCP 依赖性跨细胞调节有利于脊椎动物组织的收敛延伸。
DOI:
10.1016/j.ydbio.2018.12.017
发表时间:
2019
期刊:
Developmental biology
影响因子:
2.7
作者:
[Shindo,Asako, Inoue,Yasuhiro, Kinoshita,Makoto, Wallingford,JohnB]
通讯作者:
Wallingford,JohnB
Control of collective cell movement by planar cell polarity signaling
-
批准号:10225582
-
项目类别:
-
资助金额:$32.85万
-
财政年份:2020
-
负责人:John B Wallingford
-
依托单位:
Control of collective cell movement by planar cell polarity signaling
-
批准号:10704441
-
项目类别:
-
资助金额:$8.44万
-
财政年份:2020
-
负责人:John B Wallingford
-
依托单位:
Control of collective cell movement by planar cell polarity signaling
-
批准号:10042185
-
项目类别:
-
资助金额:$33.46万
-
财政年份:2020
-
负责人:John B Wallingford
-
依托单位:
Control of collective cell movement by planar cell polarity signaling
-
批准号:10622573
-
项目类别:
-
资助金额:$32.85万
-
财政年份:2020
-
负责人:John B Wallingford
-
依托单位:
Control of collective cell movement by planar cell polarity signaling
-
批准号:10403992
-
项目类别:
-
资助金额:$32.85万
-
财政年份:2020
-
负责人:John B Wallingford
-
依托单位:
Dynamics of vertebrate planar cell polarity proteins
-
批准号:8986583
-
项目类别:
-
资助金额:$18.77万
-
财政年份:2015
-
负责人:John B Wallingford
-
依托单位:
Control of collective cell movement by planar cell polarity signaling
-
批准号:9127983
-
项目类别:
-
资助金额:$31.68万
-
财政年份:2015
-
负责人:John B Wallingford
-
依托单位:
15th International Xenopus Conference
-
批准号:8785924
-
项目类别:
-
资助金额:$1.46万
-
财政年份:2014
-
负责人:John B Wallingford
-
依托单位:
Development and function in mucociliary epithelia
-
批准号:8714042
-
项目类别:
-
资助金额:$37.85万
-
财政年份:2013
-
负责人:John B Wallingford
-
依托单位:
Development and function in mucociliary epithelia
-
批准号:9099911
-
项目类别:
-
资助金额:$38.63万
-
财政年份:2013
-
负责人:John B Wallingford
-
依托单位:
Development and function in mucociliary epithelia
-
批准号:10658656
-
项目类别:
-
资助金额:$39.75万
-
财政年份:2013
-
负责人:John B Wallingford
-
依托单位:
Development and function in mucociliary epithelia
-
批准号:9891070
-
项目类别:
-
资助金额:$38.5万
-
财政年份:2013
-
负责人:John B Wallingford
-
依托单位:
Development and function in mucociliary epithelia
-
批准号:8583728
-
项目类别:
-
资助金额:$36.76万
-
财政年份:2013
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:7668797
-
项目类别:
-
资助金额:$4.39万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:8187241
-
项目类别:
-
资助金额:$29.93万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:8728890
-
项目类别:
-
资助金额:$29.94万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:7028253
-
项目类别:
-
资助金额:$26.38万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:6913787
-
项目类别:
-
资助金额:$27.01万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:8535270
-
项目类别:
-
资助金额:$28.92万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
Mechanism of vertebrate neural tube morphogenesis
-
批准号:7575233
-
项目类别:
-
资助金额:$28.1万
-
财政年份:2005
-
负责人:John B Wallingford
-
依托单位:
国内基金
海外基金
FGF8通过Ras/MEK/ERK信号通路调控apical ES结构影响精子生成的机制研究
-
批准号:81801519
-
项目类别:青年科学基金项目
-
资助金额:21.0万元
-
批准年份:2018
-
负责人:于岚
-
依托单位: