Interleukin-8 processing by neutrophil elastase, cathepsin G and proteinase-3

M Padrines, M Wolf, A Walz, M Baggiolini - FEBS letters, 1994 - Elsevier
M Padrines, M Wolf, A Walz, M Baggiolini
FEBS letters, 1994Elsevier
Activated neutrophils secrete two forms of IL-8 with 77 and 72 amino acids, IL-8 (77) and IL-
8 (72), along with proteinases that could process these cytokines. Significant conversion of
IL-8 (77) to more potent, N-terminally truncated forms was observed upon incubation with
neutrophil granule lysates and purified proteinase-3. IL-8 (72) was considerably more
resistant to proteolytic processing than IL-8 (77). The present observations indicate that
neutrophil proteinases released in inflamed tissues convert IL-8 to more active forms and …
Abstract
Activated neutrophils secrete two forms of IL-8 with 77 and 72 amino acids, IL-8(77) and IL-8(72), along with proteinases that could process these cytokines. Significant conversion of IL-8(77) to more potent, N-terminally truncated forms was observed upon incubation with neutrophil granule lysates and purified proteinase-3. IL-8(72) was considerably more resistant to proteolytic processing than IL-8(77). The present observations indicate that neutrophil proteinases released in inflamed tissues convert IL-8 to more active forms and therefore tend to conserve or enhance, rather than decrease IL-8 activity.
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