TY - JOUR
T1 - Fas ligand on tumor cells mediates inactivation of neutrophils
AU - Chen, Yi Ling
AU - Chen, Shun Hua
AU - Wang, Jiu Yao
AU - Yang, Bei Chang
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2003/8/1
Y1 - 2003/8/1
N2 - The expression of Fas ligand (FasL) on tumor cells (tumor FasL) has been implicated in their evasion of immune surveillance. In this study, we investigated the cellular mechanism for FasL-associated immune escape using melanoma B16F10-derived cells as a model. Transfectants carrying FasL-specific ribozymes expressed low levels of FasL (FasLlow tumor cells) as compared with those carrying enhanced green fluorescent protein-N1 plasmids (FasLhigh tumor cells). When injected s.c. into C57BL/6 mice, FasLlow tumor cells grew more slowly than did FasLhigh melanoma cells. FasLhigh tumor cells showed more intensive neutrophilic infiltration accompanied by multiple necrotizing areas than did FasLlow tumor cells. The average size of FasLlow tumors, but not of FasLhigh tumors, was significantly enhanced in mice depleted of neutrophils. Consistently, a local injection of LPS to recruit/activate neutrophils significantly delayed tumor formation by FasLlow tumor cells, and slightly retarded that of FasLhigh tumor cells in both C57BL/6 and nonobese diabetic/SCID mice. Neutrophils killed FasLlow melanoma cells more effectively than FasLhigh melanoma cells in vitro. The resistance of FasLhigh melanoma cells to being killed by neutrophils was correlated with impaired neutrophil activation, as demonstrated by reductions in gelatinase B secretion, reactive oxygen species production, and the surface expression of CD11b and the transcription of FasL. Local transfer of casein-enriched or PMA-treated neutrophils delayed tumor formation by melanoma cells. Taken together, inactivation of neutrophils by tumor FasL is an important mechanism by which tumor cells escape immune attack.
AB - The expression of Fas ligand (FasL) on tumor cells (tumor FasL) has been implicated in their evasion of immune surveillance. In this study, we investigated the cellular mechanism for FasL-associated immune escape using melanoma B16F10-derived cells as a model. Transfectants carrying FasL-specific ribozymes expressed low levels of FasL (FasLlow tumor cells) as compared with those carrying enhanced green fluorescent protein-N1 plasmids (FasLhigh tumor cells). When injected s.c. into C57BL/6 mice, FasLlow tumor cells grew more slowly than did FasLhigh melanoma cells. FasLhigh tumor cells showed more intensive neutrophilic infiltration accompanied by multiple necrotizing areas than did FasLlow tumor cells. The average size of FasLlow tumors, but not of FasLhigh tumors, was significantly enhanced in mice depleted of neutrophils. Consistently, a local injection of LPS to recruit/activate neutrophils significantly delayed tumor formation by FasLlow tumor cells, and slightly retarded that of FasLhigh tumor cells in both C57BL/6 and nonobese diabetic/SCID mice. Neutrophils killed FasLlow melanoma cells more effectively than FasLhigh melanoma cells in vitro. The resistance of FasLhigh melanoma cells to being killed by neutrophils was correlated with impaired neutrophil activation, as demonstrated by reductions in gelatinase B secretion, reactive oxygen species production, and the surface expression of CD11b and the transcription of FasL. Local transfer of casein-enriched or PMA-treated neutrophils delayed tumor formation by melanoma cells. Taken together, inactivation of neutrophils by tumor FasL is an important mechanism by which tumor cells escape immune attack.
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U2 - 10.4049/jimmunol.171.3.1183
DO - 10.4049/jimmunol.171.3.1183
M3 - Article
C2 - 12874204
AN - SCOPUS:0042847257
VL - 171
SP - 1183
EP - 1191
JO - Journal of Immunology
JF - Journal of Immunology
SN - 0022-1767
IS - 3
ER -