Complement C1q-induced activation of β-catenin signalling causes hypertensive arterial remodelling View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2015-12

AUTHORS

Tomokazu Sumida, Atsuhiko T. Naito, Seitaro Nomura, Akito Nakagawa, Tomoaki Higo, Akihito Hashimoto, Katsuki Okada, Taku Sakai, Masamichi Ito, Toshihiro Yamaguchi, Toru Oka, Hiroshi Akazawa, Jong-Kook Lee, Tohru Minamino, Stefan Offermanns, Tetsuo Noda, Marina Botto, Yoshio Kobayashi, Hiroyuki Morita, Ichiro Manabe, Toshio Nagai, Ichiro Shiojima, Issei Komuro

ABSTRACT

Hypertension induces structural remodelling of arteries, which leads to arteriosclerosis and end-organ damage. Hyperplasia of vascular smooth muscle cells (VSMCs) and infiltration of immune cells are the hallmark of hypertensive arterial remodelling. However, the precise molecular mechanisms of arterial remodelling remain elusive. We have recently reported that complement C1q activates β-catenin signalling independent of Wnts. Here, we show a critical role of complement C1-induced activation of β-catenin signalling in hypertensive arterial remodelling. Activation of β-catenin and proliferation of VSMCs were observed after blood-pressure elevation, which were prevented by genetic and chemical inhibition of β-catenin signalling. Macrophage depletion and C1qa gene deletion attenuated the hypertension-induced β-catenin signalling, proliferation of VSMCs and pathological arterial remodelling. Our findings unveil the link between complement C1 and arterial remodelling and suggest that C1-induced activation of β-catenin signalling becomes a novel therapeutic target to prevent arteriosclerosis in patients with hypertension. More... »

PAGES

6241

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/ncomms7241

DOI

http://dx.doi.org/10.1038/ncomms7241

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1037414909

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/25716000


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