Adiponectin protein exists in aortic endothelial cells.

AIMS: Inflammation is closely associated with the development of atherosclerosis and metabolic syndrome. Adiponectin, an adipose-derived secretory protein, possesses an anti-atherosclerotic property. The present study was undertaken to elucidate the presence and significance of adiponectin in vascul...

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Main Authors: Noriyuki Komura, Norikazu Maeda, Takuya Mori, Shinji Kihara, Hideaki Nakatsuji, Ayumu Hirata, Yoshihiro Tochino, Tohru Funahashi, Iichiro Shimomura
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3742782?pdf=render
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spelling doaj-ec8a8c467a8649dd8a3e20234956cd2a2020-11-24T21:12:24ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0188e7127110.1371/journal.pone.0071271Adiponectin protein exists in aortic endothelial cells.Noriyuki KomuraNorikazu MaedaTakuya MoriShinji KiharaHideaki NakatsujiAyumu HirataYoshihiro TochinoTohru FunahashiIichiro ShimomuraAIMS: Inflammation is closely associated with the development of atherosclerosis and metabolic syndrome. Adiponectin, an adipose-derived secretory protein, possesses an anti-atherosclerotic property. The present study was undertaken to elucidate the presence and significance of adiponectin in vasculature. METHODS AND RESULTS: Immunofluorescence staining was performed in aorta of wild-type (WT) mice and demonstrated that adiponectin was co-stained with CD31. Thoracic aorta was cut through and then aortic intima was carefully shaved from aorta. Western blotting showed the existence of adiponectin protein in aortic intima, while there was no adiponectin mRNA expression. Adiponectin knockout (Adipo-KO) and WT mice were administered with a low-dose and short-term lipopolysaccharide (LPS) (1 mg/kg of LPS for 4 hours). The endothelium vascular adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) were highly increased in Adipo-KO mice compared to WT mice after LPS administration. CONCLUSIONS: Adiponectin protein exists in aortic endothelium under steady state and may protect vasculature from the initiation of atherosclerosis.http://europepmc.org/articles/PMC3742782?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Noriyuki Komura
Norikazu Maeda
Takuya Mori
Shinji Kihara
Hideaki Nakatsuji
Ayumu Hirata
Yoshihiro Tochino
Tohru Funahashi
Iichiro Shimomura
spellingShingle Noriyuki Komura
Norikazu Maeda
Takuya Mori
Shinji Kihara
Hideaki Nakatsuji
Ayumu Hirata
Yoshihiro Tochino
Tohru Funahashi
Iichiro Shimomura
Adiponectin protein exists in aortic endothelial cells.
PLoS ONE
author_facet Noriyuki Komura
Norikazu Maeda
Takuya Mori
Shinji Kihara
Hideaki Nakatsuji
Ayumu Hirata
Yoshihiro Tochino
Tohru Funahashi
Iichiro Shimomura
author_sort Noriyuki Komura
title Adiponectin protein exists in aortic endothelial cells.
title_short Adiponectin protein exists in aortic endothelial cells.
title_full Adiponectin protein exists in aortic endothelial cells.
title_fullStr Adiponectin protein exists in aortic endothelial cells.
title_full_unstemmed Adiponectin protein exists in aortic endothelial cells.
title_sort adiponectin protein exists in aortic endothelial cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description AIMS: Inflammation is closely associated with the development of atherosclerosis and metabolic syndrome. Adiponectin, an adipose-derived secretory protein, possesses an anti-atherosclerotic property. The present study was undertaken to elucidate the presence and significance of adiponectin in vasculature. METHODS AND RESULTS: Immunofluorescence staining was performed in aorta of wild-type (WT) mice and demonstrated that adiponectin was co-stained with CD31. Thoracic aorta was cut through and then aortic intima was carefully shaved from aorta. Western blotting showed the existence of adiponectin protein in aortic intima, while there was no adiponectin mRNA expression. Adiponectin knockout (Adipo-KO) and WT mice were administered with a low-dose and short-term lipopolysaccharide (LPS) (1 mg/kg of LPS for 4 hours). The endothelium vascular adhesion molecule-1 (VCAM-1) and intercellular adhesion molecule-1 (ICAM-1) were highly increased in Adipo-KO mice compared to WT mice after LPS administration. CONCLUSIONS: Adiponectin protein exists in aortic endothelium under steady state and may protect vasculature from the initiation of atherosclerosis.
url http://europepmc.org/articles/PMC3742782?pdf=render
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