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-Glutamyl Transpeptidase Gene Promoters along with Differentiation of Hepatoblasts into Biliary or Hepatocytic Lineage


From Institut National de la Santé et de la Recherche
Médicale Unite 99,*
Hôpital Henri Mondor,
Université Paris XII, Créteil; and Institut National de la
Santé et de la Recherche Médicale Unite
522,
Hôpital Pontchaillou,
Rennes, France
-Glutamyl transpeptidase (GGT), a major enzyme
of glutathione (GSH) homeostasis, is often used as a biliary
marker to follow the differentiation of hepatic precursor cells. The
expression of the GGT gene is driven by different promoters and yields
multiple mRNAs, depending on the cell type or the stage of
differentiation. In the present study, we analyzed the GGT mRNA
expression pattern by quantitative reverse transcriptase-polymerase
chain reaction or by in situ hybridization i) in the
liver, in vivo, at early stages of
development; ii) in oval cells, which proliferate and
differentiate into hepatocytes in response to galactosamine injury
in vivo; and finally, iii) during hepatoblast
differentiation, in vitro. We show that GGT gene
transcription originates from promoters P3, P4, and P5
in rat hepatic precursor cells. Differentiation of these cells induces
profound alterations in GGT gene expression, leading to
extinction of promoters P4 and P5, when they differentiate into
the hepatocytic pathway, and to extinction of promoters P3 and
P5 when they differentiate into the biliary pathway. This diversity in
GGT mRNA expression provides unique molecular probes to follow hepatic
precursor cell differentiation. Furthermore, the identification
of factors governing GGT P5 and P4 promoter expression should provide
further insight into the molecular events that occur as the liver
precursor cell differentiates into the hepatic lineages.
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