Journal
BLOOD
Volume 101, Issue 8, Pages 3093-3101Publisher
AMER SOC HEMATOLOGY
DOI: 10.1182/blood-2002-08-2485
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Funding
- NCI NIH HHS [CA50239] Funding Source: Medline
- NIDDK NIH HHS [DK49786] Funding Source: Medline
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Although the functions of granzymei A and B have been defined, the functions of the other highly expressed granzymes (Gzms) of murine cytotoxic lymphocytes (C, D, and F) have not yet been evaluated. In this report, we describe the ability of murine GzmC (which is most closely related to human geanzyme H) to cause cell death. The induction of death requires its protease activity and is characterized. by the rapid externalization of phospoatidyl-serine, nuclear condensation and collapse, and single-stranded DNA nicking. The kinetics of these events are similar to those caused by granzyme B, and its potency (defined on molar basis) is also equivalent. The induction of death did not involve the activation of caspases, the cleavage of BID, or the activation of the CAD nuclease. However, granzyme C did cause rapid mitochondrial swelling and depolarization in intact cells or in isolated mitochondria, and this mitochondrial damage was not prevented by cycldsporin A pretreatment. These results suggest that granzyme C rapidly induces target cell death by attacking nuclear and mitochondrial targets and that these tar gets are distinct from those, used by granzyme B to cause classical apoptosis. (C) 2003 by The American Society of Hematology.
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