Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.

Cysteine-rich protein 61 (Cyr61) is a secreted matrix-associated protein that regulates a broad spectrum of biological and cellular activities. This study aimed to investigate the role of Cyr61 in progressive kidney fibrosis induced by unilateral ureteral obstruction (UUO) surgery in mice. The expre...

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Main Authors: Chun-Fu Lai, Yung-Ming Chen, Wen-Chih Chiang, Shuei-Liong Lin, Min-Liang Kuo, Tun-Jun Tsai
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3574066?pdf=render
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author Chun-Fu Lai
Yung-Ming Chen
Wen-Chih Chiang
Shuei-Liong Lin
Min-Liang Kuo
Tun-Jun Tsai
author_facet Chun-Fu Lai
Yung-Ming Chen
Wen-Chih Chiang
Shuei-Liong Lin
Min-Liang Kuo
Tun-Jun Tsai
author_sort Chun-Fu Lai
collection DOAJ
description Cysteine-rich protein 61 (Cyr61) is a secreted matrix-associated protein that regulates a broad spectrum of biological and cellular activities. This study aimed to investigate the role of Cyr61 in progressive kidney fibrosis induced by unilateral ureteral obstruction (UUO) surgery in mice. The expression of Cyr61 transcripts and proteins in the obstructed kidneys were increased from day 1 and remained high until day 10 after surgery. Immunohistochemistry indicated that Cyr61 was expressed mainly in renal tubular epithelial cells. The upregulated Cyr61 in UUO kidneys was reduced in mice treated with pan-transforming growth factor-β (TGF-β) antibody. The role of TGF-β in tubular Cyr61 upregulation after obstructive kidney injury was further supported by experiments showing that TGF-β1 stimulated Cyr61 expression in cultured tubular epithelial cells. Notably, the upregulation of Cyr61 in UUO kidneys was followed by a marked increase in monocyte chemoattractant protein 1 (MCP-1) transcripts and macrophage infiltration, which were attenuated in mice treated with anti-Cyr61 antibodies. This proinflammatory property of Cyr61 in inducing MCP-1 expression was further confirmed in tubular epithelial cells cultured with Cyr61 protein. The anti-Cyr61 antibody in UUO mice also reduced the levels of collagen type 1-α1 transcripts, collagen fibril accumulation evaluated by picrosirius red staining, and the levels of α-smooth muscle actin (α-SMA) transcripts and proteins on day 4 after surgery; however, the antifibrotic effect was not sustained. In conclusion, the TGF-β-mediated increase in tubular Cyr61 expression involved renal inflammatory cell infiltration through MCP-1 induction during obstructive kidney injury. The Cyr61 blockade attenuated kidney fibrosis in the early phase, but the antifibrotic effect could not be sustained.
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spelling doaj.art-b14ebb732edd4d829361d0d48c301f5c2022-12-21T18:47:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0182e5648110.1371/journal.pone.0056481Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.Chun-Fu LaiYung-Ming ChenWen-Chih ChiangShuei-Liong LinMin-Liang KuoTun-Jun TsaiCysteine-rich protein 61 (Cyr61) is a secreted matrix-associated protein that regulates a broad spectrum of biological and cellular activities. This study aimed to investigate the role of Cyr61 in progressive kidney fibrosis induced by unilateral ureteral obstruction (UUO) surgery in mice. The expression of Cyr61 transcripts and proteins in the obstructed kidneys were increased from day 1 and remained high until day 10 after surgery. Immunohistochemistry indicated that Cyr61 was expressed mainly in renal tubular epithelial cells. The upregulated Cyr61 in UUO kidneys was reduced in mice treated with pan-transforming growth factor-β (TGF-β) antibody. The role of TGF-β in tubular Cyr61 upregulation after obstructive kidney injury was further supported by experiments showing that TGF-β1 stimulated Cyr61 expression in cultured tubular epithelial cells. Notably, the upregulation of Cyr61 in UUO kidneys was followed by a marked increase in monocyte chemoattractant protein 1 (MCP-1) transcripts and macrophage infiltration, which were attenuated in mice treated with anti-Cyr61 antibodies. This proinflammatory property of Cyr61 in inducing MCP-1 expression was further confirmed in tubular epithelial cells cultured with Cyr61 protein. The anti-Cyr61 antibody in UUO mice also reduced the levels of collagen type 1-α1 transcripts, collagen fibril accumulation evaluated by picrosirius red staining, and the levels of α-smooth muscle actin (α-SMA) transcripts and proteins on day 4 after surgery; however, the antifibrotic effect was not sustained. In conclusion, the TGF-β-mediated increase in tubular Cyr61 expression involved renal inflammatory cell infiltration through MCP-1 induction during obstructive kidney injury. The Cyr61 blockade attenuated kidney fibrosis in the early phase, but the antifibrotic effect could not be sustained.http://europepmc.org/articles/PMC3574066?pdf=render
spellingShingle Chun-Fu Lai
Yung-Ming Chen
Wen-Chih Chiang
Shuei-Liong Lin
Min-Liang Kuo
Tun-Jun Tsai
Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
PLoS ONE
title Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
title_full Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
title_fullStr Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
title_full_unstemmed Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
title_short Cysteine-rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis.
title_sort cysteine rich protein 61 plays a proinflammatory role in obstructive kidney fibrosis
url http://europepmc.org/articles/PMC3574066?pdf=render
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