Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0189088
Title: Visualizing the spatiotemporal map of Rac activation in bovine aortic endothelial cells under laminar and disturbed flows
Authors: Shao S.
Xiang C. 
Qin K.
Aziz A.U.R.
Liao X.
Liu B.
Keywords: alcohol
benzene
cholesterol
nocodazole
Rac protein
Rac protein
animal cell
Article
BAEC cell line
bovine
cell membrane
cell membrane fluidity
cell polarity
controlled study
cytoskeleton
disturbed flow
flow rate
fluorescence microscopy
genetic transfection
laminar flow
microtubule
nonhuman
physical parameters
protein interaction
reporter gene
shear stress
animal
aorta
cytology
membrane fluidity
metabolism
vascular endothelium
Animals
Aorta
Cattle
Endothelium, Vascular
Membrane Fluidity
rac GTP-Binding Proteins
Issue Date: 2017
Citation: Shao S., Xiang C., Qin K., Aziz A.U.R., Liao X., Liu B. (2017). Visualizing the spatiotemporal map of Rac activation in bovine aortic endothelial cells under laminar and disturbed flows. PLoS ONE 12 (11) : e0189088. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0189088
Rights: Attribution 4.0 International
Abstract: Disturbed flow can eliminate the alignment of endothelial cells in the direction of laminar flow, and significantly impacts on atherosclerosis in collateral arteries near the bifurcation and high curvature regions. While shear stress induced Rac polarity has been shown to play crucial roles in cell polarity and migration, little is known about the spatiotemporal map of Rac under disturbed flow, and the mechanism of flow-induced cell polarity still needs to be elucidated. In this paper, disturbed flow or laminar flow with 15 dyn/cm 2 of average shear stress was applied on bovine aortic endothelial cells (BAECs) for 30 minutes. A genetically-encoded PAK-PBD-GFP reporter was transfected into BAECs to visualize the real-time activation of Rac in living cell under fluorescence microscope. The imaging of the fluorescence intensity was analyzed by Matlab and the normalized data was converted into 3D spatiotemporal map. Then the changes of data upon chemical interference were fitted with logistic curve to explore the rule and mechanism of Rac polarity under laminar or disturbed flow. A polarized Rac activation was observed at the downstream edge along the laminar flow, which was enhanced by benzol alcohol-enhanced membrane fluidity but inhibited by nocodazole-disrupted microtubules or cholesterol-inhibited membrane fluidity, while no obvious polarized Rac activation could be found upon disturbed flow application. It is concluded that disturbed flow inhibits the flow-induced Rac polarized activation, which is related to the interaction of cell membrane and cytoskeleton, especially the microtubules. © 2017 Shao et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161165
ISSN: 19326203
DOI: 10.1371/journal.pone.0189088
Rights: Attribution 4.0 International
Appears in Collections:Elements
Staff Publications

Show full item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1371_journal_pone_0189088.pdf8.77 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons