Literature DB >> 17164408

Activation of the IGF1 system characterizes cholangiocyte survival during progression of primary biliary cirrhosis.

Paolo Onori1, Domenico Alvaro, Anna Rosa Floreani, Maria Grazia Mancino, Antonio Franchitto, Maria Guido, Guido Carpino, Adriano De Santis, Mario Angelico, Adolfo F Attili, Eugenio Gaudio.   

Abstract

We evaluated the IGF1 system in cholangiocytes of primay biliary cirrhosis (PBC) patients and investigated the relationships with apoptosis. Biopsies of PBC patients (n=32) and normal subjects (n=5) were investigated by immunohistochemistry for expression in cholangiocytes of IGF1, IGF1-R, pAKT, terminal deoxynucleotide transferase end labeling (TUNEL), Bax (proapoptotic protein), and Bcl2 (antiapoptotic protein). Whereas normal cholangiocytes were almost negative, cholangiocytes of PBC patients showed strong IHC staining for IGF1, IGF1-R, and pAKT, which increases from stage I to stage IV, where >70% of cholangiocytes were positive. Bax/Bcl2 ratio reached the highest value (4.6) in PBC stage III when apoptosis is maximal (24% TUNEL positivity), whereas it declines in stage IV (1.4) when only 7.8% cholangiocytes were TUNEL positive. In PBC stages III and IV, expression of IGF1, IGF1-R, and pAKT in cholangiocytes was directly correlated with the antiapoptotic Bcl2 and inversely correlated with proapoptotic Bax, Bax/Bcl2 ratio, and TUNEL positivity. In conclusion, cholangiocytes of PBC patients showed a marked increase in IGF1, IGF1-R, and pAKT expression involving most cholangiocytes surviving in the terminal ductopenic stage. This was associated and correlated with a balance of pro- and antiapoptotic proteins favoring survival rather than apoptosis, suggesting a major role of IGF1 system in promoting cholangiocyte survival.

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Year:  2006        PMID: 17164408     DOI: 10.1369/jhc.6R7125.2006

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  19 in total

1.  MicroRNA profiling identifies miR-29 as a regulator of disease-associated pathways in experimental biliary atresia.

Authors:  Nicholas J Hand; Amber M Horner; Zankhana R Master; LaTasha A Boateng; Claire LeGuen; Marina Uvaydova; Joshua R Friedman
Journal:  J Pediatr Gastroenterol Nutr       Date:  2012-02       Impact factor: 2.839

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Journal:  Am J Pathol       Date:  2010-08-19       Impact factor: 4.307

Review 3.  Pathogenesis of primary biliary cirrhosis.

Authors:  David E J Jones
Journal:  Gut       Date:  2007-07-19       Impact factor: 23.059

4.  Etiopathogenesis of primary biliary cirrhosis: an overview of recent developments.

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Journal:  Am J Pathol       Date:  2020-04-07       Impact factor: 4.307

6.  Role of sex hormones in the modulation of cholangiocyte function.

Authors:  Romina Mancinelli; Paolo Onori; Sharon Demorrow; Heather Francis; Shannon Glaser; Antonio Franchitto; Guido Carpino; Gianfranco Alpini; Eugenio Gaudio
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Review 7.  Polycystic liver diseases.

Authors:  P Onori; A Franchitto; R Mancinelli; G Carpino; D Alvaro; H Francis; G Alpini; E Gaudio
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8.  Repression of CFTR activity in human MMNK-1 cholangiocytes induces sulfotransferase 1E1 expression in co-cultured HepG2 hepatocytes.

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Journal:  Biochim Biophys Acta       Date:  2008-09-11

9.  Morphological and functional features of hepatic cyst epithelium in autosomal dominant polycystic kidney disease.

Authors:  Domenico Alvaro; Paolo Onori; Gianfranco Alpini; Antonio Franchitto; Douglas M Jefferson; Alessia Torrice; Vincenzo Cardinale; Fabrizio Stefanelli; Maria Grazia Mancino; Mario Strazzabosco; Mario Angelico; Adolfo Attili; Eugenio Gaudio
Journal:  Am J Pathol       Date:  2008-01-17       Impact factor: 4.307

10.  Epigenetic reprogramming of IGF1 and leptin genes by serum deprivation in multipotential mesenchymal stromal cells.

Authors:  Cecilia Sanchez; Adam Oskowitz; Radhika R Pochampally
Journal:  Stem Cells       Date:  2009-02       Impact factor: 6.277

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