Granzyme serine proteases in inflammation and rheumatic diseases.
Alexandre AubertKaren JungSho HiroyasuJulian PardoDavid J GranvillePublished in: Nature reviews. Rheumatology (2024)
Granzymes (granule-secreted enzymes) are a family of serine proteases that have been viewed as redundant cytotoxic enzymes since their discovery more than 30 years ago. Predominantly produced by cytotoxic lymphocytes and natural killer cells, granzymes are delivered into the cytoplasm of target cells through immunological synapses in cooperation with the pore-forming protein perforin. After internalization, granzymes can initiate cell death through the cleavage of intracellular substrates. However, evidence now also demonstrates the existence of non-cytotoxic, pro-inflammatory, intracellular and extracellular functions that are granzyme specific. Under pathological conditions, granzymes can be produced and secreted extracellularly by immune cells as well as by non-immune cells. Depending on the granzyme, accumulation in the extracellular milieu might contribute to inflammation, tissue injury, impaired wound healing, barrier dysfunction, osteoclastogenesis and/or autoantigen generation.
Keyphrases
- oxidative stress
- cell death
- natural killer cells
- cell cycle arrest
- induced apoptosis
- wound healing
- small molecule
- reactive oxygen species
- protein kinase
- high throughput
- peripheral blood
- dna binding
- protein protein
- signaling pathway
- amino acid
- lps induced
- pi k akt
- endoplasmic reticulum stress
- inflammatory response
- cell proliferation
- single cell