| Literature DB >> 11081635 |
B Motyka1, G Korbutt, M J Pinkoski, J A Heibein, A Caputo, M Hobman, M Barry, I Shostak, T Sawchuk, C F Holmes, J Gauldie, R C Bleackley.
Abstract
The serine proteinase granzyme B is crucial for the rapid induction of target cell apoptosis by cytotoxic T cells. Granzyme B was recently demonstrated to enter cells in a perforin-independent manner, thus predicting the existence of a cell surface receptor(s). We now present evidence that this receptor is the cation-independent mannose 6-phosphate/insulin-like growth factor receptor (CI-MPR). Inhibition of the granzyme B-CI-MPR interaction prevented granzyme B cell surface binding, uptake, and the induction of apoptosis. Significantly, expression of the CI-MPR was essential for cytotoxic T cell-mediated apoptosis of target cells in vitro and for the rejection of allogeneic cells in vivo. These results suggest a novel target for immunotherapy and a potential mechanism used by tumors for immune evasion.Entities:
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Year: 2000 PMID: 11081635 DOI: 10.1016/s0092-8674(00)00140-9
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582