Intercellular communication via the endo-lysosomal system: translocation of granzymes through membrane barriers

SE Stewart, ME D'Angelo, PI Bird - … et Biophysica Acta (BBA)-Proteins and …, 2012 - Elsevier
Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics, 2012Elsevier
Cytotoxic lymphocytes (CLs) are responsible for the clearance of virally infected or
neoplastic cells. CLs possess specialised lysosome-related organelles called granules
which contain the granzyme family of serine proteases and perforin. Granzymes may induce
apoptosis in the target cell when delivered by the pore forming protein, perforin. Here we
follow the perforin-granzyme pathway from synthesis and storage in the granule, to
exocytosis and finally delivery into the target cell. This review focuses on the controversial …
Cytotoxic lymphocytes (CLs) are responsible for the clearance of virally infected or neoplastic cells. CLs possess specialised lysosome-related organelles called granules which contain the granzyme family of serine proteases and perforin. Granzymes may induce apoptosis in the target cell when delivered by the pore forming protein, perforin. Here we follow the perforin-granzyme pathway from synthesis and storage in the granule, to exocytosis and finally delivery into the target cell. This review focuses on the controversial subject of perforin-mediated translocation of granzymes into the target cell cytoplasm. It remains unclear whether this occurs at the cell surface with granzymes moving through a perforin pore in the plasma membrane, or if it involves internalisation of perforin and granzymes and subsequent release from an endocytic compartment. The latter mechanism would represent an example of cross talk between the endo-lysosomal pathways of individual cells. This article is part of a Special Issue entitled: Proteolysis 50years after the discovery of lysosome.
Elsevier
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