Secreted Ectodomain of SIGLEC-9 and MCP-1 Synergistically Improve Acute Liver Failure in Rats by Altering Macrophage Polarity

Sci Rep. 2017 Mar 8:7:44043. doi: 10.1038/srep44043.

Abstract

Effective treatments for acute liver failure (ALF) are still lacking. We recently reported that a single intravenous administration of serum-free conditioned medium from stem cells derived from human exfoliated deciduous teeth (SHED-CM) into the D-galactosamine (D-Gal)-induced rat ALF model improves the liver injury. However, the specific factors in SHED-CM that are responsible for resolving ALF remain unclear. Here we found that depleting SHED-CM of two anti-inflammatory M2 macrophage inducers-monocyte chemoattractant protein-1 (MCP-1) and the secreted ectodomain of sialic acid-binding Ig-like lectin-9 (sSiglec-9)-abolished its ability to resolve rat ALF. Furthermore, treatment with MCP-1/sSiglec-9 alone dramatically improved the survival of ALF rats. This treatment induced anti-inflammatory M2, suppressed hepatocyte apoptosis, and promoted hepatocyte proliferation. Treatment with an M2-depletion reagent (mannosylated clodronate liposomes) suppressed the recovery. In addition, MCP-1 and sSiglec-9 synergistically promoted the M2 differentiation of bone marrow-derived macrophages via CCR2, accompanied by the production of multiple liver-regenerating factors. The conditioned medium from MCP-1/sSiglec-9-activated M2 macrophages, but not from interleukin-4-induced ones, suppressed the D-Gal- and LPS-induced apoptosis of primary hepatocytes and promoted their proliferation in vitro. The unique combination of MCP-1/sSiglec-9 ameliorates rat ALF by inhibiting hepatocellular apoptosis and promoting liver regeneration through the induction of anti-inflammatory/tissue-repairing M2 macrophages.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Cell Proliferation
  • Chemokine CCL2 / metabolism*
  • Culture Media, Serum-Free
  • Female
  • Inflammation / complications
  • Inflammation / metabolism
  • Liver Failure, Acute / complications
  • Liver Failure, Acute / metabolism*
  • Macrophages / metabolism*
  • Rats, Sprague-Dawley
  • Sialic Acid Binding Immunoglobulin-like Lectins / metabolism*
  • Stem Cells / physiology
  • Tooth Exfoliation
  • Tooth, Deciduous / cytology

Substances

  • Ccl2 protein, rat
  • Chemokine CCL2
  • Culture Media, Serum-Free
  • Sialic Acid Binding Immunoglobulin-like Lectins
  • Siglec-9 protein, rat