basic FUNCTION
| serine protease necessary for target cell lysis in cell-mediated immune responses |
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critical role for GZMA and GZMB in dictating immunogenicity by influencing the mode of tumor cell death, indicating that granzymes contribute to the efficient generation of immune effector pathways in addition to their well-known role in apoptosis induction |
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inducing apoptosis of target cells in conjunction with perforin |
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role for granzyme B in the regulatory T cell compartment in immune regulation to viral infections |
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endogenous GZMB can play a promigratory role, at least in part through cleaving FGFR1 |
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GZMB-mediated cleavage of fibronectin contributes to attenuated angiogenesis through the disruption of endothelial cell - fibronectin interaction resulting in impaired endothelial cell migration and tubular formation |
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from cytotoxic T lymphocyte (CTLS) acts double roles to keratinocytes: a IL18 converting enzyme and pro-apoptotic factor in the skin inflammatory diseases |
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is an immune-derived serine protease that accumulates in the extracellular matrix (ECM) during chronic inflammation and is capable of cleaving fibronectin (FN) |
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is a modulator of vascular response during chronic inflammation |
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GZMB-induced mitochondrial ROS are required for apoptosis |
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significant role for GZMB in Extracellular matrix (ECM) degradation that may have implications in many age-related chronic inflammatory diseases |
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is a protease with a well-characterized intracellular role in targeted destruction of compromised cells by cytotoxic lymphocytes |
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also cleaves extracellular matrix components, suggesting that it influences the interplay between cytotoxic lymphocytes and their environment |
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important role for GZMB in expediting cytotoxic lymphocyte diapedesis via basement membrane remodeling |
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is a serine protease involved in cell-mediated cytotoxicity in conjunction with the pore-forming protein, perforin |
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also likely contributes to matrix remodeling and fibrosis through an extracellular, perforin-independent process |
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perforin-independent, extracellular role for GZMB in the pathogenesis of cardiac fibrosis |