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1 Department of Gastroenterology, University of Heidelberg, D-69115 Heidelberg, Germany; and 2 Intestinal Disease Research Program, McMaster University Medical Centre, Hamilton, Ontario, Canada L8N-3Z5
As yet, little is known about the function of the glia of the
enteric nervous system (ENS), particularly in an immune-stimulated environment. This prompted us to study the potential of cultured enteroglial cells for cytokine synthesis and secretion. Jejunal myenteric plexus preparations from adult rats were enzymatically dissociated, and enteroglial cells were purified by complement-mediated cytolysis and grown in tissue culture. Cultured cells were stimulated with recombinant rat interleukin (IL)-1
, IL-6, and tumor necrosis factor (TNF)-
, and IL-6 mRNA expression and secretion were assessed using RT-PCR and a bioassay, respectively. Stimulation with TNF-
did
not affect IL-6 mRNA expression, whereas IL-1
stimulated IL-6 mRNA
and protein synthesis in a time- and concentration-dependent fashion.
In contrast, IL-6 significantly and dose-dependently suppressed IL-6
mRNA expression. In summary, we have presented evidence that enteric
glial cells are a potential source of IL-6 in the myenteric plexus and
that cytokine production by enteric glial cells can be regulated by
cytokines. These findings strongly support the contention that enteric
glial cells act as immunomodulatory cells in the enteric nervous system.
enteric glia; tissue culture
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