Please use this identifier to cite or link to this item: https://doi.org/10.3389/fphys.2017.00963
DC FieldValue
dc.titleNear-wall migration dynamics of erythrocytes in vivo: Effects of cell deformability and arteriolar bifurcation
dc.contributor.authorNamgung B.
dc.contributor.authorNg Y.C.
dc.contributor.authorLeo H.L.
dc.contributor.authorRifkind J.M.
dc.contributor.authorKim S.
dc.date.accessioned2020-09-09T10:33:01Z
dc.date.available2020-09-09T10:33:01Z
dc.date.issued2017
dc.identifier.citationNamgung B., Ng Y.C., Leo H.L., Rifkind J.M., Kim S. (2017). Near-wall migration dynamics of erythrocytes in vivo: Effects of cell deformability and arteriolar bifurcation. Frontiers in Physiology 8 (NOV) : 963. ScholarBank@NUS Repository. https://doi.org/10.3389/fphys.2017.00963
dc.identifier.issn1664-042X
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/175413
dc.description.abstractRed blood cell (RBC) deformability has a significant impact on microcirculation by affecting cell dynamics. Despite previous studies that have demonstrated the margination of rigid cells and particles in vitro, little information is available on the in vivo margination of deformability-impaired RBCs under physiological flow and hematocrit conditions. Thus, in this study, we examined how the deformability-dependent, RBC migration alters the cell distribution under physiological conditions, particularly in arteriolar network flows. The hardened RBCs (hRBCs) were found to preferentially flow near the vessel walls of small arterioles (diameter = 47.1-93.3 ?m). The majority of the hRBCs (63%) were marginated within the range of 0.7R-0.9R (R: radial position normalized by vessel radius), indicating that the hRBCs preferentially accumulated near the vessel walls. The laterally marginated hRBCs maintained their lateral positions near the walls while traversing downstream with attenuated radial dispersion. In addition, the immediate displacement of RBCs while traversing a bifurcation also contributes to the near-wall accumulation of hRBCs. The notable difference in the inward migration between the marginated nRBCs and hRBCs after bifurcations further supports the potential role of bifurcations in the accumulation of hRBCs near the walls. © 2017 Namgung, Ng, Leo, Rifkind and Kim.
dc.sourceUnpaywall 20200831
dc.subjectarteriole
dc.subjectblood vessel wall
dc.subjectcell migration
dc.subjectcellular distribution
dc.subjecterythrocyte deformability
dc.subjecthemodynamics
dc.subjecthuman cell
dc.subjectin vivo study
dc.subjectmicrocirculation
dc.typeArticle
dc.contributor.departmentBIOMED INST FOR GLOBAL HEALTH RES & TECH
dc.contributor.departmentDEPARTMENT OF COMPUTER SCIENCE
dc.contributor.departmentBIOMEDICAL ENGINEERING
dc.description.doi10.3389/fphys.2017.00963
dc.description.sourcetitleFrontiers in Physiology
dc.description.volume8
dc.description.issueNOV
dc.description.page963
dc.published.statePublished
Appears in Collections:Staff Publications
Elements

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_3389_fphys_2017_00963.pdf1.65 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.