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Expression of granzyme B in peripheral blood polymorphonuclear neutrophils (PMN), myeloid cell lines and in PMN derived from haemotopoietic stem cells in vitro
被引:18
|作者:
Wagner, Christof
[1
,2
]
Stegmaier, Sabine
[1
]
Haensch, Gertrud Maria
[1
]
机构:
[1] Heidelberg Univ, Inst Immunol, D-60120 Heidelberg, Germany
[2] Berufsgenossensch Unfallklin Ludwigshafen, Klin Ulfallchirurg & Orthopadie, Ludwigshafen, Germany
关键词:
polymorphonuclear neutrophils;
cytotoxicity;
granzyme B;
CD34+stem cell;
HL-60;
U937;
D O I:
10.1016/j.molimm.2007.09.033
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Granzyme B and perforin are the major protagonists of cytotoxicity mediated by natural killer (NK) cells or cytotoxic T cells. More recent we described the presence of granzyme B and perform in polymorphonuclear neutrophils (PMN), a finding in discrepancy with the credo that granzyme B and perform expression is restricted to cytotoxic T cells and NK cells. In extension of our previous study, we now provide evidence that granzyme B is not only present in mature PMN, but also in the myeloid cell lines HL-60 and U937, in CD34+ stem cells, and in PMN derived from CD34+ cells in vitro. In agreement with the "targeting by time" hypothesis we found the bulk of granzyme B in association with primary granules, in addition to a minor membrane expression. Granzyme B, on one hand might, enhance the cytotoxic potential of PMN, on the other, it may provide PMN with additional means to degrade extracellular matrices. (c) 2007 Elsevier Ltd. All rights reserved.
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页码:1761 / 1766
页数:6
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