Increased ADAMTS-13 proteolytic activity in rat hepatic stellate cells upon activation in vitro and in vivo

Academic Article

Abstract

  • Introduction: ADAMTS-13 is a member of A DisintegrinAndMetalloprotease withThromboSpondin type 1 repeats (ADAMTS) family, primarily synthesized in hepatic stellate cells (HSCs), one of the major cell types transdifferentiating into myofibroblasts during liver fibrosis. However, the association between ADAMTS-13 expression and HSC activation or liver fibrosis is not known. Methods: In this study, we determined the ADAMTS-13 mRNA, protein, and activity in isolated primary HSCs upon activation on a plastic dish and in liver after administration of carbon tetrachloride (CCl4) in rats. Results: We showed that ADAMTS-13 antigen and proteolytic activity in the activated rat HSCs were dramatically increased, whereas ADAMTS-13mRNAin these cells was only minimally altered. Similarly, the ADAMTS-13 antigen and proteolytic activity in rat liver after CCl4 injury were also significantly increased, whereas the ADAMTS-13 mRNAs in these liver tissues were only slightly increased compared with normal. Surprisingly, despite the dramatic up-regulation of ADAMTS-13 protein synthesis in the activated HSCs after CCl4 administration, the plasma levels of ADAMTS-13 protease in rats did not increase concordantly. Conclusion: We conclude that the up-regulation of ADAMTS-13 protein expression in rat HSCs during activation in vitro and in vivo suggests the possibility ofADAMTS-13 proteolysis, an important part of function of the activated HSCs, perhaps through modulation of liver regeneration or formation of liver fibrosis after various injuries. The data also suggest the minimal contribution of the activated HSCs in regulation of plasma levels of ADAMTS-13 protease. © 2006 International Society on Thrombosis and Haemostasis.
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    Digital Object Identifier (doi)

    Author List

  • Niiya M; Uemura M; Zheng XW; Pollak ES; Dockal M; Scheiflinger F; Wells RG; Zheng XL
  • Start Page

  • 1063
  • End Page

  • 1070
  • Volume

  • 4
  • Issue

  • 5