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Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis.

Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Research Abstract Details 

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  • Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Abstract Text:

    youngmi jungYoungmi Jung,shannon j mccallShannon J McCall,yin-xiong liYin-Xiong Li,anna mae diehlAnna Mae Diehl,

    Indian Hedgehog (Ihh) regulates tissue morphogenesis. Hedgehog (Hh) activity has been demonstrated in human cholangiocarcinoma and hepatocellular carcinoma lines, and in myofibroblasts and progenitors from adult rodent livers. We evaluated Hh pathway involvement in the response to biliary injury in primary biliary cirrhosis (PBC). Liver sections from 3 PBC patients and 3 controls without liver disease were studied. Immunohistochemistry was used to determine if cells that accumulate in PBC livers express Ihh or Hh-target genes including the Hh-receptor, Patched (Ptc), and the Hh-transcriptional activator glioblastoma (Gli) 2. Positive cells were further identified by costaining for cytokeratin (CK) 19, a biliary marker, or OV6, a hepatic progenitor marker. In all subjects, Gli2 and Ptc expression localized in portal areas. The numbers of Gli2- or Ptc-expressing cells/portal triad were each 10-fold greater in patients with PBC than in controls (P<0.05). In PBC livers, some CK19+ cells coexpressed Gli2 or Ptc. Many stromal fibroblastic cells were also Gli2+. Strong Ihh expression was detected in most bile ductular cells. Scattered stromal cells also expressed Ihh. The number of Ihh+ cells/portal triad was 6-fold greater in PBC livers than controls (P<0.05). OV6+ progenitors increased significantly in PBC livers, and some of these cells coexpressed Ihh, Ptc, and/or Gli2. Conclusion: This is the first direct evidence that noncancerous, adult human livers harbor several types of cells that produce and/or respond to Hh ligands. Such Hh-responsive cells accumulate during the fibroproliferative response to chronic cholestatic liver injury, suggesting a role for Hh signaling in this process.

    Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Publishing Authors By Initials

    y jungY Jung,sj mccallSJ McCall,yx liYX Li,am diehlAM Diehl,

    For similar cells: connective tissue cells: stromal cells research abstracts see: cells: connective tissue cells: stromal cells research

    PUBMED ID PMID:

    MEDLINE DATE:

    Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Journal Published:

    PUBLICATION TYPE: Research Support, N.I.H., Extr

    Journal: Hepatology (Baltimore, Md.)

    VOLUME: 45

    Page Numbers: 1091-6

    Journal Abbreviation:

    ISSN: 0270-9139

    DAY: 3

    MONTH: May

    YEAR: 2007

    Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 8302946

    Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Keywords Mesh Terms:

    KEYWORDS: Stromal Cells

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis. Information

    Substance Name: patched receptors

    Registry Number: 0

    Grant and Affiliation Information for Bile ductules and stromal cells express hedgehog ligands and/or hedgehog target genes in primary biliary cirrhosis.

    AFFILIATION: Division of Gastroenterology, Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA.

    Country: United States

    United States Research PublicationUnited States Research Publication

    AGENCY: United States NIAAA

    GRANT: 5R01-AA010154-11

    ACRONYM: AA

    MEDLINETA: Hepatology

    REFSOURCE:

    DATABASENAME:

    ACCESSION NUMBER:

    Number Hits: 0

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