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Keywords {🔍}

liver, pge, msc, levels, article, nlrp, alf, fig, macrophage, group, pubmed, signaling, inflammation, tak, macrophages, mscderived, inflammasome, activation, cell, google, scholar, cells, bmdm, role, injury, cas, msccox, polarization, expression, mice, confirmed, mtor, protein, stem, death, inflammatory, ilβ, treated, mesenchymal, hepatocyte, results, epi, nanjing, mrna, study, studies, serum, inhibitor, nfκb, acute,

Topics {✒️}

lps/d-gal-induced liver injury lps/d-gal-induced alf based lps/d-gal-induced alf bone marrow-derived macrophage tgf-β-activated kinase 1 prostaglandin e2 secreted exosomal mir-146a contributes mesenchymal stem cell mesenchymal stem cells lps/d-gal administration lps/d-gal treatment macrophage colony-stimulating factor hepatic ischemia/reperfusion injury mesenchymal stromal cells acetaminophen-induced liver injury article download pdf inhibiting tak1-nf-κb signaling mitogen-activated protein kinases full size image lps/d-gal cell stem cell liver ischemia-reperfusion injury goat anti-rabbit igg goat anti-rat igg acute liver failure enzyme-linked immunosorbent assay msc-derived pge2 protected real-time quantitative pcr prostaglandin e2 receptor msc secreted pge2 nf-κb signaling substrates secret anti-inflammatory cytokines tak1-nf-κb pathway nf-κb signaling inhibition chronic liver failure xiaolei shi designed acute liver injury macrophage polarized activation immune-mediated liver injury ischemia/reperfusion injury nf-κb signaling plays important pro-inflammatory cytokines chronic liver fibrosis prostaglandin e2 tunel-stained liver sections privacy choices/manage cookies msc-derived pge2 administered ep4-specific antagonist hepatocyte apoptosis induced d-gal

Questions {❓}

• Acute liver failure: a curable disease by 2024?

Schema {🗺️}

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         headline:Mesenchymal stem cell-secreted prostaglandin E2 ameliorates acute liver failure via attenuation of cell death and regulation of macrophage polarization
         description:Acute liver failure (ALF) is an acute inflammatory liver disease with high mortality. Previous preclinical and clinical trials have confirmed that mesenchymal stem cell (MSC) is a promising therapeutic approach; however, the effect is not satisfied as the underlying molecular mechanisms of MSC in treating ALF remain unclear. MSC isolated from 4- to 6-week-old C57BL/6 mice were used to treat ALF. Histological and serological parameters were analyzed to evaluate the efficacy of MSC. We explored the molecular mechanism of MSC in the treatment of ALF by detecting liver inflammatory response and hepatocyte death. In this study, we found that the therapeutic potential of MSC on ALF is dependent on the secretion of prostaglandin E2 (PGE2), a bioactive lipid. MSC-derived PGE2 inhibited TGF-β-activated kinase 1 (TAK1) signaling and NLRP3 inflammasome activation in liver macrophages to decrease the production of inflammatory cytokines. Meanwhile, macrophages in the liver could be induced to anti-inflammatory (M2) macrophages by MSC-derived PGE2 via STAT6 and mechanistic target of rapamycin (mTOR) signaling, which then promote inflammatory resolution and limit liver injury. Finally, administrating EP4 antagonist significantly ameliorated the therapeutic ability of MSC, which promoted liver inflammation and decreased M2 macrophages. Our results indicate that PGE2 might be a novel important mediator of MSC in treating ALF, which is through inhibiting the liver inflammatory response and hepatocyte death.
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      headline:Mesenchymal stem cell-secreted prostaglandin E2 ameliorates acute liver failure via attenuation of cell death and regulation of macrophage polarization
      description:Acute liver failure (ALF) is an acute inflammatory liver disease with high mortality. Previous preclinical and clinical trials have confirmed that mesenchymal stem cell (MSC) is a promising therapeutic approach; however, the effect is not satisfied as the underlying molecular mechanisms of MSC in treating ALF remain unclear. MSC isolated from 4- to 6-week-old C57BL/6 mice were used to treat ALF. Histological and serological parameters were analyzed to evaluate the efficacy of MSC. We explored the molecular mechanism of MSC in the treatment of ALF by detecting liver inflammatory response and hepatocyte death. In this study, we found that the therapeutic potential of MSC on ALF is dependent on the secretion of prostaglandin E2 (PGE2), a bioactive lipid. MSC-derived PGE2 inhibited TGF-β-activated kinase 1 (TAK1) signaling and NLRP3 inflammasome activation in liver macrophages to decrease the production of inflammatory cytokines. Meanwhile, macrophages in the liver could be induced to anti-inflammatory (M2) macrophages by MSC-derived PGE2 via STAT6 and mechanistic target of rapamycin (mTOR) signaling, which then promote inflammatory resolution and limit liver injury. Finally, administrating EP4 antagonist significantly ameliorated the therapeutic ability of MSC, which promoted liver inflammation and decreased M2 macrophages. Our results indicate that PGE2 might be a novel important mediator of MSC in treating ALF, which is through inhibiting the liver inflammatory response and hepatocyte death.
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      name:Department of Hepatobiliary Surgery, Nanjing University of Chinese Medicine, Nanjing, China
      name:Department of Hepatobiliary Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China
      name:Department of Hepatobiliary Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing University of Chinese Medicine, Nanjing, China
      name:Department of Hepatobiliary Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing University of Chinese Medicine, Nanjing, China
      name:Department of Hepatobiliary Surgery, Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing Drum Tower Hospital Clinical College of Nanjing Medical University, Nanjing, China
      name:Department of Hepatobiliary Surgery, Nanjing University of Chinese Medicine, Nanjing, China

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