Over expression of proteins that alter the intracellular signaling pathways in the cytoplasm of the liver cells forming Mallory-Denk bodies

Exp Mol Pathol. 2017 Feb;102(1):106-114. doi: 10.1016/j.yexmp.2017.01.011. Epub 2017 Jan 13.

Abstract

In this study, liver biopsy sections fixed in formalin and embedded in paraffin (FFPE) from patients with alcoholic hepatitis (AH) were used. The results showed that the expression of the SYK protein was up regulated by RNA-seq and real time PCR analyses in the alcoholic hepatitis patients compared to controls. The results were supported by using the IHC fluorescent antibody staining intensity morphometric quantitation. Morphometric quantification of fluorescent intensity measurement showed a two fold increase in SYK protein in the cytoplasm of the cells forming MDBs compared to surrounding normal hepatocytes. The expression of AKT1 was also analyzed. AKT1 is a serine/threonine-specific protein kinase that plays a key role in multiple cellular processes such as glucose metabolism, apoptosis, cell proliferation, transcription and cell migration. The AKT protein was also increased in hepatocyte balloon cells forming MDBs. This observation demonstrates the role of SYK and its subsequent effect on the internal signaling pathways such as PI3K/AKT as well as p70S6K, as a potential multifunctional target in protein quality control mechanisms of hepatocytes when ER stress is activated.

Keywords: AKT1; Alcoholic hepatitis; Mallory-Denk bodies; SYK.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Biopsy
  • Cytoplasm / genetics
  • Cytoplasm / metabolism*
  • Hepatitis, Alcoholic / genetics
  • Hepatitis, Alcoholic / metabolism
  • Hepatitis, Alcoholic / pathology
  • Hepatocytes / metabolism
  • Humans
  • Immunoblotting
  • Immunohistochemistry
  • Liver / metabolism*
  • Liver / pathology
  • Mallory Bodies / metabolism*
  • Phosphatidylinositol 3-Kinases / genetics
  • Phosphatidylinositol 3-Kinases / metabolism
  • Proto-Oncogene Proteins c-akt / biosynthesis*
  • Proto-Oncogene Proteins c-akt / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Ribosomal Protein S6 Kinases, 70-kDa / genetics
  • Ribosomal Protein S6 Kinases, 70-kDa / metabolism
  • Signal Transduction*
  • Syk Kinase / biosynthesis*
  • Syk Kinase / genetics

Substances

  • Phosphatidylinositol 3-Kinases
  • SYK protein, human
  • Syk Kinase
  • AKT1 protein, human
  • Proto-Oncogene Proteins c-akt
  • Ribosomal Protein S6 Kinases, 70-kDa