Faculty Research & Creative Activity

Document Type

Article

Publication Date

January 2007

Abstract

Dedifferentiated hepatoma cells, in contrast to most other cell types including hepatoma cells, undergo apoptosis when treated with lipopolysaccharide (LPS) plus the protein synthesis inhibitor cycloheximide (CHx). We recently reported that the dedifferentiated hepatoma cells also exhibit a strong and prolonged NF-jB induction phenotype upon exposure to LPS, suggesting that NF-jB signaling may play a pro-survival role, as reported in several other cell systems. To test the role of NF-jB in preventing LPS-mediated apoptosis, we examined the dedifferentiated cell line M38. Results show that antioxidants strongly inhibited LPS + CHx-mediated cell death in the M38 cells, yet only modestly inhibited NF-jB induction. In addition, inhibition of NF-jB translocation by infection of the M38 cells with an adenoviral vector expressing an IjBa super-repressor did not result in LPS-mediated cell death. These results suggest that unlike TNFa induction, the cell survival pathway activated in response to LPS is independent of NF-jB translocation in the dedifferentiated cells. Addition of inhibitors of JNK, p38 and ERK pathways also failed to elicit LPS-mediated apoptosis similar to that observed when protein synthesis is prevented. Thus, cell survival pathways other than those involving NF-jB inducible gene expression or other well-known pathways appear to be involved in protecting the dedifferentiated hepatoma variant cells from LPS-mediated apoptosis. Importantly, this pro-apoptotic function of LPS appears to be a function of loss of hepatic gene expression, as the parental hepatoma cells resist LPSmediated apoptosis in the presence of protein synthesis inhibitors.

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This peer-reviewed article is also available full text at http://www.bioscirep.org/bsr/027/0235/0270235.pdf DOI 10.1007/s10540-007-9049-9

https://works.bepress.com/gary_bulla/2/

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