Overexpression of apelin receptor (APJ/AGTRL1) on hepatic stellate cells and sinusoidal angiogenesis in human cirrhotic liver View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2010-08-20

AUTHORS

Hiroaki Yokomori, Masaya Oda, Kazunori Yoshimura, Sanae Machida, Fumihiko Kaneko, Toshifumi Hibi

ABSTRACT

BackgroundThe apelin receptor (APJ) is related to angiotensin-like-receptor 1 (AGTRL1). This study was designed to elucidate the in vivo localization and changes of APJ in cirrhotic liver, and the in vitro changes of APJ expression in cultured hepatic stellate cells (HSCs) and capillarized sinusoidal endothelial cells (SECs) activated by growth factors.MethodsIn vivo studies used control liver samples, cirrhotic liver samples from patients with Child’s A cirrhosis undergoing surgical resection (Child-A-LC), and cirrhotic liver samples from autopsied cases of decompensated Child’s C cirrhosis (Child-C-LC). Immunohistochemical (IHC), Western blot, laser-capture microdissection (LCM) coupled with reverse transcription -polymerase chain reaction (RT-PCR), and immunoelectron microscopic (IEM) studies for APJ expression were conducted. In vitro examinations used commercial human HSCs and SECs. APJ expression was examined in cultured HSCs activated by growth factors and in capillarized SECs activated by angiogenic factors.ResultsThe IHC study of liver samples revealed only slight APJ expression in hepatic sinusoids in control liver tissue. In cirrhotic liver (Child-A-LC and Child-C-LC), APJ expression was evident mainly along the sinusoids and on portal fibroblasts in fibrotic septa. Western blot analysis of whole-liver homogenate and LCM–PCR of sinusoids revealed overexpression of APJ in Child-C-LC samples. The results of IEM studies showed that APJ expression was increased significantly on HSCs, but it was sparse on SECs in Child-C-LC tissue. In vitro examination revealed that APJ was overexpressed in cultured HSCs activated by platelet-derived growth factor-β.ConclusionsEnhanced expression of APJ on HSCs in cirrhosis indicates markedly increased vascular remodeling. More... »

PAGES

222-231

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00535-010-0296-3

DOI

http://dx.doi.org/10.1007/s00535-010-0296-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1019946732

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/20725750


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