Natural killer cell-derived human granzyme H induces an alternative, caspase-independent cell-death program.

Abstract:

:Granzyme H (GzmH) belongs to a family of 5 human serine proteases that are expressed by cytotoxic immune effector cells. Although GzmH is most closely related to the caspase-activating granzyme B (GzmB), neither a natural substrate nor a role in immune defense reactions has been demonstrated for this orphan granzyme. In rodents, multiple related genes exist, but none of these can be regarded as functional homologs. Here we show that host cells are efficiently killed by GzmH after perforin and streptolysin O-mediated delivery into the cytosol. Dying cells show typical hallmarks of programmed cell death, such as mitochondrial depolarization, reactive oxygen species (ROS) generation, DNA degradation, and chromatin condensation. Contrary to GzmB, cell death by GzmH does not involve the activation of executioner caspases, the cleavage of Bid or inhibitor of caspase-activated DNase (ICAD), or the release of cytochrome c. The high expression levels of GzmH in naive natural killer (NK) cells and its potent killing ability strongly support the role of the protease in triggering an alternative cell-death pathway in innate immunity.

journal_name

Blood

journal_title

Blood

authors

Fellows E,Gil-Parrado S,Jenne DE,Kurschus FC

doi

10.1182/blood-2006-10-051649

subject

Has Abstract

pub_date

2007-07-15 00:00:00

pages

544-52

issue

2

eissn

0006-4971

issn

1528-0020

pii

blood-2006-10-051649

journal_volume

110

pub_type

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