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Originally published online as doi:10.1189/jlb.0203079 on October 2, 2003

Published online before print October 2, 2003
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(Journal of Leukocyte Biology. 2004;75:87-98.)
© 2004 by Society for Leukocyte Biology

Apoptosis-induced proteinase 3 membrane expression is independent from degranulation

Stéphanie Durant*, Magali Pederzoli*, Yves Lepelletier{dagger}, Sandrine Canteloup*, Patrick Nusbaum*, Philippe Lesavre* and Véronique Witko-Sarsat*,1

* INSERM U507 and
{dagger} UMR/CNRS2444, Hôpital Necker, Paris, France

1Correspondence: INSERM U507, Hôpital Necker, 161, rue de Sèvres, 75015 Paris, France. E-mail: witko-sarsat{at}necker.fr

Proteinase 3 (PR3) and human neutrophil elastase (HNE) are serine proteinases stored in the azurophilic granules of neutrophils. In contrast to HNE, PR3 is the target of antineutrophil cytoplasm antibodies (ANCA) in Wegener’s granulomatosis. The mechanisms leading to the membrane expression of PR3 and HNE are still unclear and appear to be critical to understand the pathophysiological role of ANCA. Stably transfected rat basophilic cell lines (RBL) with PR3 or HNE were used to analyze the PR3 and HNE secretion mechanisms and differentiate between them. RBL cells were lacking endogenous PR3 and HNE. They were stably transfected with HNE or PR3 or an inactive mutant of PR3 (PR3S203A). Using the calcium ionophore A23187 as a secretagogue, higher serine proteinase activity was secreted in the supernatant of RBL/HNE than in RBL/PR3. It is interesting that PR3 and PR3/S203A were also expressed at the plasma membrane, thus demonstrating that serine protease activity was not required for plasma membrane expression. In contrast, no expression of plasma membrane HNE could be detected in RBL/HNE. Apoptosis induced by etoposide was evaluated by DNA fragmentation, the presence of cytoplasmic histone-associated DNA fragments, and annexin V labeling. No membrane HNE was detected in RBL/HNE. In contrast, in RBL/PR3 and in RBL/PR3S203A, the membrane expression of PR3 and PR3S203A increased with etoposide concentrations and appeared closely related to annexin V labeling. Our data suggest that membrane PR3 originates from two distinct pools, the granular pool mobilized following degranulation or a plasma membrane pool mobilized upon apoptosis.

Key Words: inflammation • Wegener • neutrophil • elastase • annexin V • RBL




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