Connective tissue growth factor is correlated with peritoneal lymphangiogenesis.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
21 08 2019
Historique:
received: 14 08 2018
accepted: 07 08 2019
entrez: 23 8 2019
pubmed: 23 8 2019
medline: 23 10 2020
Statut: epublish

Résumé

Lymphatic absorption in the peritoneal cavity may contribute to ultrafiltration failure in peritoneal dialysis (PD). Lymphatic vessels develop during PD-related peritoneal fibrosis. Connective tissue growth factor (CTGF, also called CCN2) is an important determinant of fibrotic tissue remodeling, but little is known about its possible involvement in lymphangiogenesis. In this study, we investigated the relationship between CTGF and peritoneal lymphangiogenesis. A positive correlation was observed between vascular endothelial growth factor-C (VEGF-C), a major lymphangiogenic growth factor, and the CTGF concentration in human PD effluents. CTGF expression was positively correlated with expression of lymphatic markers and VEGF-C in human peritoneal biopsies. We found a positive correlation between the increase in CTGF and the increase in VEGF-C in cultured human peritoneal mesothelial cells (HPMCs) treated with transforming growth factor-β1 (TGF-β1). The diaphragm is a central player in peritoneal lymphatic absorption. CTGF expression was also correlated with expression of VEGF-C and lymphatics in a rat diaphragmatic fibrosis model induced by chlorhexidine gluconate (CG). Furthermore, CTGF gene deletion reduced VEGF-C expression and peritoneal lymphangiogenesis in the mouse CG model. Inhibition of CTGF also reduced VEGF-C upregulation in HPMCs treated with TGF-β1. Our results suggest a close relationship between CTGF and PD-associated lymphangiogenesis.

Identifiants

pubmed: 31434958
doi: 10.1038/s41598-019-48699-9
pii: 10.1038/s41598-019-48699-9
pmc: PMC6704065
doi:

Substances chimiques

RNA, Small Interfering 0
Transforming Growth Factor beta1 0
Vascular Endothelial Growth Factor C 0
Connective Tissue Growth Factor 139568-91-5
chlorhexidine gluconate MOR84MUD8E
Chlorhexidine R4KO0DY52L

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

12175

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Auteurs

Hiroshi Kinashi (H)

Department of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan.
Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Naohiro Toda (N)

Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Ting Sun (T)

Department of Nephrology and Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Tri Q Nguyen (TQ)

Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Yasuhiro Suzuki (Y)

Department of Nephrology and Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Takayuki Katsuno (T)

Department of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan.

Hideki Yokoi (H)

Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Jan Aten (J)

Department of Pathology, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.

Masashi Mizuno (M)

Department of Nephrology and Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Shoichi Maruyama (S)

Department of Nephrology and Renal Replacement Therapy, Nagoya University Graduate School of Medicine, Nagoya, Japan.

Motoko Yanagita (M)

Department of Nephrology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Roel Goldschmeding (R)

Department of Pathology, University Medical Center Utrecht, Utrecht, The Netherlands.

Yasuhiko Ito (Y)

Department of Nephrology and Rheumatology, Aichi Medical University, Nagakute, Japan. yasuito@aichi-med-u.ac.jp.

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