Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.

Lipid rafts (LRs) are dynamic, sterol- and sphingolipid-enriched nanodomains involved in the regulation of cellular functions and signal transduction, that upon stimuli, via (e.g. association of raft proteins and lipids), may cluster into domains of submicron or micron scale. Up to date, however, li...

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Main Authors: Marta Pilarczyk, Lukasz Mateuszuk, Anna Rygula, Mariusz Kepczynski, Stefan Chlopicki, Malgorzata Baranska, Agnieszka Kaczor
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4148353?pdf=render
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spelling doaj-bba95e5ae9f44a3484b1a91dfbb3a1372020-11-25T01:11:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0198e10606510.1371/journal.pone.0106065Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.Marta PilarczykLukasz MateuszukAnna RygulaMariusz KepczynskiStefan ChlopickiMalgorzata BaranskaAgnieszka KaczorLipid rafts (LRs) are dynamic, sterol- and sphingolipid-enriched nanodomains involved in the regulation of cellular functions and signal transduction, that upon stimuli, via (e.g. association of raft proteins and lipids), may cluster into domains of submicron or micron scale. Up to date, however, lipid raft clusters were observed only under artificially promoted conditions and their formation in vivo has not been confirmed. Using non-destructive approach involving Raman and Atomic Force Microscopy imaging we demonstrated the presence of clustered lipid rafts in endothelium of the aorta of the db/db mice that represent a reliable murine model of type 2 diabetes. The raft clusters in the aorta of diabetic mice were shown to occupy a considerably larger (about 10-fold) area of endothelial cells surface as compared to the control. Observation of pathology-promoted LRs confirms that the cellular increase of lipid content results in clustering of LRs. Clustering of LRs leads to the formation of assemblies with diameters up to 3 micrometers and increased lipid character. This massive clustering of lipid rafts in diabetes may trigger a signaling cascade leading to vascular inflammation.http://europepmc.org/articles/PMC4148353?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Marta Pilarczyk
Lukasz Mateuszuk
Anna Rygula
Mariusz Kepczynski
Stefan Chlopicki
Malgorzata Baranska
Agnieszka Kaczor
spellingShingle Marta Pilarczyk
Lukasz Mateuszuk
Anna Rygula
Mariusz Kepczynski
Stefan Chlopicki
Malgorzata Baranska
Agnieszka Kaczor
Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
PLoS ONE
author_facet Marta Pilarczyk
Lukasz Mateuszuk
Anna Rygula
Mariusz Kepczynski
Stefan Chlopicki
Malgorzata Baranska
Agnieszka Kaczor
author_sort Marta Pilarczyk
title Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
title_short Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
title_full Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
title_fullStr Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
title_full_unstemmed Endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
title_sort endothelium in spots--high-content imaging of lipid rafts clusters in db/db mice.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Lipid rafts (LRs) are dynamic, sterol- and sphingolipid-enriched nanodomains involved in the regulation of cellular functions and signal transduction, that upon stimuli, via (e.g. association of raft proteins and lipids), may cluster into domains of submicron or micron scale. Up to date, however, lipid raft clusters were observed only under artificially promoted conditions and their formation in vivo has not been confirmed. Using non-destructive approach involving Raman and Atomic Force Microscopy imaging we demonstrated the presence of clustered lipid rafts in endothelium of the aorta of the db/db mice that represent a reliable murine model of type 2 diabetes. The raft clusters in the aorta of diabetic mice were shown to occupy a considerably larger (about 10-fold) area of endothelial cells surface as compared to the control. Observation of pathology-promoted LRs confirms that the cellular increase of lipid content results in clustering of LRs. Clustering of LRs leads to the formation of assemblies with diameters up to 3 micrometers and increased lipid character. This massive clustering of lipid rafts in diabetes may trigger a signaling cascade leading to vascular inflammation.
url http://europepmc.org/articles/PMC4148353?pdf=render
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