Upregulation of C-Reactive Protein by Placenta-Derived Mesenchymal Stem Cells Promotes Angiogenesis in A Rat Model with Cirrhotic Liver

  • Ji Hye Jun
  • , Jieun Jung
  • , Jae Yeon Kim
  • , Seong Gyu Hwang
  • , Si Hyun Bae
  • , Gi Jin Kim

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Background and Objectives: Liver cirrhosis is accompanied by abnormal vascular shunts. The Wnt pathway is essential for endothelial cell survival and proliferation. C-reactive protein (CRP), which is produced by hepatocyte, activates angiogenesis in cardiovascular diseases. Methods and Results: The expression of CRP in CCl4-injured rat livers was detected using qRT-PCR and Western blotting after transplantation of placenta-derived mesenchymal stem cells (PD-MSCs) into rats. To determine whether CRP functions in hepatic regeneration by promoting angiogenesis through the Wnt pathway, we detected VEGF and β-catenin in liver tissues and BrdU and β-catenin in hepatocytes by immunofluorescence. The expression levels of CRP, Wnt pathway-related and angiogenic factors were increased in CCl4-injured and PD-MSCs transplanted rat livers. In vitro, the expression levels of Wnt signaling and angiogenic factors were decreased in siRNA-CRP-transfected rat hepatocytes. Conclusions: CRP upregulation by PD-MSCs participates in vascular remodeling to promote liver regeneration via the Wnt signaling pathway during hepatic failure.

Original languageEnglish
Pages (from-to)404-413
Number of pages10
JournalInternational Journal of Stem Cells
Volume13
Issue number3
DOIs
StatePublished - Nov 2020

Bibliographical note

Publisher Copyright:
© 2020 ⓒ 2020 by the Korean Society for Stem Cell Research This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Keywords

  • C-reactive protein
  • Liver cirrhosis
  • Placenta-derived mesenchymal stem cells
  • Vascular remodeling
  • Wnt pathway

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