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Liver Center and Department of Medicine, University of California, San Francisco, California 94110
Hepatic stellate
cells are widely recognized for their contribution to liver fibrosis.
This study investigated whether these cells also promote hepatic
inflammation by producing neutrophil chemoattractants. Specifically,
stellate cells were examined as potential sources of cytokine-induced
neutrophil chemoattractant (CINC), a rat chemokine resembling human
interleukin-8. Stellate cells from normal rat liver expressed little or
no CINC. In culture, CINC mRNA was induced rapidly, coinciding with the
phenomenon of culture activation. CINC mRNA rose 4.6-fold within 3 days
and was accompanied by secretion of immunoreactive and biologically active CINC protein (4.1 ng · µg
DNA
1 · day
1).
Studies in vivo demonstrated that CINC could be induced in stellate
cells during liver injury. CINC mRNA rose significantly (4- to 6-fold)
in two models of liver disease, both of which cause stellate cell
activation. In summary, the data indicate that CINC is induced during
stellate cell activation in culture and in vivo. They suggest that
stellate cell-derived CINC can promote hepatic inflammation in vivo.
chemokine; chemotaxis; leukocyte; inflammation
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