Epiplakin1 is expressed in the cholangiocyte lineage cells in normal liver and adult progenitor cells in injured liver

Gene Expr Patterns. 2011 Mar-Apr;11(3-4):255-62. doi: 10.1016/j.gep.2011.01.001. Epub 2011 Jan 7.

Abstract

We have previously identified Epiplakin1 (Eppk1) as a gene expressed in pancreatic progenitor cells. Here we studied the expression of Eppk1 in developing and regenerating livers in mice. Eppk1 is initially expressed in the early bipotential hepatoblasts and is later confined to the cholangiocytes. After birth, Eppk1 is expressed in the bile duct. In the livers of mice fed with a choline-deficient ethionine-supplemented (CDE) diet, Eppk1-positive cells dramatically increase in number. The Eppk1-positive cells express A6, thereby indicating that they are hepatic progenitor cells. Other cholangiocyte markers, such as Cytokeratins, E-cadherin, osteopontin and Sox9, are also co-expressed in the hepatic progenitor cells. Some of the Eppk1-positive cells express PCNA, a proliferation marker, thereby suggesting their identities as transient amplifying cells. In conclusion, we have shown that Eppk1 serves as a useful marker for detecting the hepatic progenitor population in the developing and adult liver. The use of Eppk1 as a marker will facilitate studies of mouse hepatic progenitor cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult Stem Cells / cytology
  • Adult Stem Cells / metabolism
  • Animals
  • Antigens, Differentiation / metabolism*
  • Autoantigens / metabolism*
  • Bile Ducts / cytology
  • Bile Ducts / metabolism*
  • Cadherins / metabolism
  • Calcium-Binding Proteins / metabolism
  • Cell Lineage
  • Epithelium / metabolism
  • Fatty Liver / metabolism
  • Fatty Liver / pathology
  • Intercellular Signaling Peptides and Proteins / metabolism
  • Liver / cytology*
  • Liver / embryology
  • Liver / injuries
  • Liver Regeneration / genetics
  • Membrane Proteins / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Serrate-Jagged Proteins
  • Stem Cells / cytology
  • Stem Cells / metabolism*

Substances

  • Antigens, Differentiation
  • Autoantigens
  • Cadherins
  • Calcium-Binding Proteins
  • Intercellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Serrate-Jagged Proteins
  • epiplakin