Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep21362
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dc.titleThree-Dimensional Characterization of Mechanical Interactions between Endothelial Cells and Extracellular Matrix during Angiogenic Sprouting
dc.contributor.authorDu Y.
dc.contributor.authorHerath S.C.B.
dc.contributor.authorWang Q.-G.
dc.contributor.authorWang D.-A.
dc.contributor.authorAsada H.H.
dc.contributor.authorChen P.C.Y.
dc.date.accessioned2020-09-02T06:58:07Z
dc.date.available2020-09-02T06:58:07Z
dc.date.issued2016
dc.identifier.citationDu Y., Herath S.C.B., Wang Q.-G., Wang D.-A., Asada H.H., Chen P.C.Y. (2016). Three-Dimensional Characterization of Mechanical Interactions between Endothelial Cells and Extracellular Matrix during Angiogenic Sprouting. Scientific Reports 6 : 21362. ScholarBank@NUS Repository. https://doi.org/10.1038/srep21362
dc.identifier.issn20452322
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174022
dc.description.abstractWe studied the three-dimensional cell-extracellular matrix interactions of endothelial cells that form multicellular structures called sprouts. We analyzed the data collected in-situ from angiogenic sprouting experiments and identified the differentiated interaction behavior exhibited by the tip and stalk cells. Moreover, our analysis of the tip cell lamellipodia revealed the diversity in their interaction behavior under certain conditions (e.g., when the heading of a sprout is switched approximately between the long-axis direction of two different lamellipodia). This study marks the first time that new characteristics of such interactions have been identified with shape changes in the sprouts and the associated rearrangements of collagen fibers. Clear illustrations of such changes are depicted in three-dimensional views. © 2016, Nature Publishing Group. All rights reserved.
dc.sourceUnpaywall 20200831
dc.subjectbehavior
dc.subjectcollagen fiber
dc.subjectendothelium cell
dc.subjectextracellular matrix
dc.subjectgene rearrangement
dc.subjecthuman
dc.subjecthuman cell
dc.subjectlamellipodium
dc.subjectsprout
dc.subjectsprouting
dc.subjectangiogenesis
dc.subjectbiomechanics
dc.subjectcell communication
dc.subjectcell line
dc.subjectcell motion
dc.subjectchemistry
dc.subjectendothelium cell
dc.subjectextracellular matrix
dc.subjectfluorescence imaging
dc.subjectfluorescent antibody technique
dc.subjectlab on a chip
dc.subjectmetabolism
dc.subjectphysiology
dc.subjectpseudopodium
dc.subjectthree dimensional imaging
dc.subjectultrastructure
dc.subjectbaysilon
dc.subjectcollagen
dc.subjectdimeticone
dc.subjectBiomechanical Phenomena
dc.subjectCell Communication
dc.subjectCell Line
dc.subjectCell Movement
dc.subjectCollagen
dc.subjectDimethylpolysiloxanes
dc.subjectEndothelial Cells
dc.subjectExtracellular Matrix
dc.subjectFluorescent Antibody Technique
dc.subjectHumans
dc.subjectImaging, Three-Dimensional
dc.subjectLab-On-A-Chip Devices
dc.subjectNeovascularization, Physiologic
dc.subjectOptical Imaging
dc.subjectPseudopodia
dc.typeArticle
dc.contributor.departmentMECHANICAL ENGINEERING
dc.description.doi10.1038/srep21362
dc.description.sourcetitleScientific Reports
dc.description.volume6
dc.description.page21362
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