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Proteomics reveals acute pro‐inflammatory and protective responses in rat Kupffer cells and hepatocytes after chemical initiation of liver cancer and after LPS and IL‐6
Author(s) -
Lorenz Olga,
Parzefall Wolfram,
Kainzbauer Eveline,
Wimmer Helge,
GraslKraupp Bettina,
Gerner Christopher,
SchulteHermann Rolf
Publication year - 2009
Publication title -
proteomics – clinical applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.948
H-Index - 54
eISSN - 1862-8354
pISSN - 1862-8346
DOI - 10.1002/prca.200800173
Subject(s) - inflammation , carcinogen , shotgun proteomics , proteomics , in vivo , biology , carcinogenesis , hepatocyte , chemistry , cancer research , microbiology and biotechnology , cancer , in vitro , immunology , biochemistry , genetics , gene
Inflammation is a key event in the development of liver cancer. We studied early inflammatory responses of Kupffer cells (KCs) and hepatocyte (HC) after cancer initiation. The chemical carcinogen N‐nitrosomorpholine (NNM) was used in a rat model. We applied a comprehensive analytical strategy including metabolic labeling, 2‐D PAGE, LC‐MS/MS‐based spot identification and shotgun proteomics and thus determined the rates of synthesis of individual proteins, compared whole tissue with isolated constituent cells and performed in vivo to in vitro comparisons of NNM effects. NNM increased synthesis of overall and 138 individual proteins identified in HC and/or KC, indicating reprogramming of metabolism favoring protection, repair and replacement of cell constituents in HC and KC. Secretome analysis by 2‐D PAGE and shotgun proteomics of HC revealed the induction of acute phase proteins, in case of KC of proteases, cytokines and chemokines, indicating inflammatory effects. All responses were induced rapidly, independently of signals from other cells, and closely mimicked the pro‐inflammatory and protective effects of inflammation modulators LPS in KC and IL‐6 in HC. In conclusion, the carcinogen NNM exerts pro‐inflammatory effects in the liver, partially by direct activation of KC. The acute inflammation and its protective component will enhance formation, survival and proliferation of initiated cells and may therefore act synergistically with the genotoxic action of the carcinogen.