Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.

A hallmark of immune cell trafficking is directional guidance via gradients of soluble or surface bound chemokines. Vascular endothelial cells produce, transport and deposit either their own chemokines or chemokines produced by the underlying stroma. Endothelial heparan sulfate (HS) was suggested to...

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Main Authors: Liat Stoler-Barak, Christine Moussion, Elias Shezen, Miki Hatzav, Michael Sixt, Ronen Alon
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3899079?pdf=render
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spelling doaj-a30dc7c8e5324b89a3b2a55bab35894a2020-11-24T21:54:20ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0191e8569910.1371/journal.pone.0085699Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.Liat Stoler-BarakChristine MoussionElias ShezenMiki HatzavMichael SixtRonen AlonA hallmark of immune cell trafficking is directional guidance via gradients of soluble or surface bound chemokines. Vascular endothelial cells produce, transport and deposit either their own chemokines or chemokines produced by the underlying stroma. Endothelial heparan sulfate (HS) was suggested to be a critical scaffold for these chemokine pools, but it is unclear how steep chemokine gradients are sustained between the lumenal and ablumenal aspects of blood vessels. Addressing this question by semi-quantitative immunostaining of HS moieties around blood vessels with a pan anti-HS IgM mAb, we found a striking HS enrichment in the basal lamina of resting and inflamed post capillary skin venules, as well as in high endothelial venules (HEVs) of lymph nodes. Staining of skin vessels with a glycocalyx probe further suggested that their lumenal glycocalyx contains much lower HS density than their basolateral extracellular matrix (ECM). This polarized HS pattern was observed also in isolated resting and inflamed microvascular dermal cells. Notably, progressive skin inflammation resulted in massive ECM deposition and in further HS enrichment around skin post capillary venules and their associated pericytes. Inflammation-dependent HS enrichment was not compromised in mice deficient in the main HS degrading enzyme, heparanase. Our results suggest that the blood vasculature patterns steep gradients of HS scaffolds between their lumenal and basolateral endothelial aspects, and that inflammatory processes can further enrich the HS content nearby inflamed vessels. We propose that chemokine gradients between the lumenal and ablumenal sides of vessels could be favored by these sharp HS scaffold gradients.http://europepmc.org/articles/PMC3899079?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Liat Stoler-Barak
Christine Moussion
Elias Shezen
Miki Hatzav
Michael Sixt
Ronen Alon
spellingShingle Liat Stoler-Barak
Christine Moussion
Elias Shezen
Miki Hatzav
Michael Sixt
Ronen Alon
Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
PLoS ONE
author_facet Liat Stoler-Barak
Christine Moussion
Elias Shezen
Miki Hatzav
Michael Sixt
Ronen Alon
author_sort Liat Stoler-Barak
title Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
title_short Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
title_full Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
title_fullStr Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
title_full_unstemmed Blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
title_sort blood vessels pattern heparan sulfate gradients between their apical and basolateral aspects.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description A hallmark of immune cell trafficking is directional guidance via gradients of soluble or surface bound chemokines. Vascular endothelial cells produce, transport and deposit either their own chemokines or chemokines produced by the underlying stroma. Endothelial heparan sulfate (HS) was suggested to be a critical scaffold for these chemokine pools, but it is unclear how steep chemokine gradients are sustained between the lumenal and ablumenal aspects of blood vessels. Addressing this question by semi-quantitative immunostaining of HS moieties around blood vessels with a pan anti-HS IgM mAb, we found a striking HS enrichment in the basal lamina of resting and inflamed post capillary skin venules, as well as in high endothelial venules (HEVs) of lymph nodes. Staining of skin vessels with a glycocalyx probe further suggested that their lumenal glycocalyx contains much lower HS density than their basolateral extracellular matrix (ECM). This polarized HS pattern was observed also in isolated resting and inflamed microvascular dermal cells. Notably, progressive skin inflammation resulted in massive ECM deposition and in further HS enrichment around skin post capillary venules and their associated pericytes. Inflammation-dependent HS enrichment was not compromised in mice deficient in the main HS degrading enzyme, heparanase. Our results suggest that the blood vasculature patterns steep gradients of HS scaffolds between their lumenal and basolateral endothelial aspects, and that inflammatory processes can further enrich the HS content nearby inflamed vessels. We propose that chemokine gradients between the lumenal and ablumenal sides of vessels could be favored by these sharp HS scaffold gradients.
url http://europepmc.org/articles/PMC3899079?pdf=render
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