Factors affecting Caco-2 intestinal epithelial cell interleukin-6 secretion

SJD Vitkus, SA Hanifin, DW McGee - In Vitro Cellular & Developmental …, 1998 - Springer
SJD Vitkus, SA Hanifin, DW McGee
In Vitro Cellular & Developmental Biology-Animal, 1998Springer
Intestinal epithelial cells (IEC) have previously been shown to produce several cytokines
including interleukin-6 (IL-6). However, many factors which may regulate IL-6 secretion by
human IEC still remain a mystery due in part to the lack of appropriate model cell lines and
the difficulty of culturing human IEC over long periods of time. We have determined that the
human colonic carcinoma cell line Caco-2 is capable of secreting IL-6 when stimulated by
the inflammatory cytokines IL-1β or tumor necrosis factor-α (TNF-α), and stimulation of these …
Summary
Intestinal epithelial cells (IEC) have previously been shown to produce several cytokines including interleukin-6 (IL-6). However, many factors which may regulate IL-6 secretion by human IEC still remain a mystery due in part to the lack of appropriate model cell lines and the difficulty of culturing human IEC over long periods of time. We have determined that the human colonic carcinoma cell line Caco-2 is capable of secreting IL-6 when stimulated by the inflammatory cytokines IL-1β or tumor necrosis factor-α (TNF-α), and stimulation of these cells with IL-1β plus TNF-α induced a synergistic enhancement of IL-6 secretion. The inflammatory cytokine-induced enhancement in IL-6 secretion was greatest when the cells were cultured in a 10% CO2 atmosphere as compared to cells grown in 5% CO2, suggesting that environmental CO2 levels may affect IEC cytokine secretion. Finally, long-term culture of the Caco-2 cells to induce cellular differentiation had no effect on the capacity of these cells to produce IL-6, indicating that the regulation of IL-6 secretion was not affected by differentiation. Taken together, these studies provide important information on the factors which regulate IL-6 secretion by human IEC as they may contribute to the cytokine network during a mucosal inflammation. The results also suggest that the Caco-2 cell line is an appropriate model for further studies on the regulation of cytokine secretion by human IEC.
Springer