New paradigm for lymphocyte granule-mediated cytotoxicity. Target cells bind and internalize granzyme B, but an endosomolytic agent is necessary for cytosolic delivery and subsequent apoptosis

Lymphocyte granule-mediated apoptosis is postulated to entail the formation of membrane pores by perforin. Then soluble granzyme reaches the cytosol either through these pores or by reparative pinocytosis. We demonstrate here that Jurkat cells bind and internalize granzyme B via high affinity bindin...

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Bibliographic Details
Published in:The Journal of biological chemistry 1996-11, Vol.271 (46), p.29073-29079
Main Authors: Froelich, C J, Orth, K, Turbov, J, Seth, P, Gottlieb, R, Babior, B, Shah, G M, Bleackley, R C, Dixit, V M, Hanna, W
Format: Article
Language:English
Subjects:
Apoptosis
Cytoplasmic Granules - immunology
Cytotoxicity, Immunologic
Endocytosis
Granzymes
Humans
Jurkat Cells
Lymphocytes - enzymology
Lymphocytes - immunology
Serine Endopeptidases - metabolism
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Summary:Lymphocyte granule-mediated apoptosis is postulated to entail the formation of membrane pores by perforin. Then soluble granzyme reaches the cytosol either through these pores or by reparative pinocytosis. We demonstrate here that Jurkat cells bind and internalize granzyme B via high affinity binding sites without toxic consequence. Apoptosis occurs, however, if sublytic perforin is added to targets washed free of soluble granzyme B. We suggest that granule-mediated apoptosis mimics viral strategies for cellular entry. Accordingly, co-internalization of granzyme B with adenovirus, a virus that escapes endosomes to reach the cytosol, also induced apoptosis. Poly(ADP-ribose) polymerase cleavage and processing of CPP32, ICE-LAP3, and Mch2 were detected at 30 min, while cytosolic acidification and DNA fragmentation occurred at 60 min. Annexin V binding and membrane permeabilization arose at 4 h. The concurrent activation of the Ced-3 proteases differed from the rate at which each cysteine protease is cleaved in vitro by granzyme B. Thus, granzyme B may not directly process these proteases in whole cells but rather may function by activating a more proximal enzyme. These results indicate that adenovirus-mediated delivery of granzyme B is suitable for elucidating biochemical events that accompany granule-mediated apoptosis.
ISSN:0021-9258
DOI:10.1074/jbc.271.46.29073