T cell lysis of murine renal cancer: multiple signaling pathways for cell death via Fas

Citation
Tj. Sayers et al., T cell lysis of murine renal cancer: multiple signaling pathways for cell death via Fas, J LEUK BIOL, 68(1), 2000, pp. 81-86
Citations number
28
Categorie Soggetti
Immunology
Journal title
JOURNAL OF LEUKOCYTE BIOLOGY
ISSN journal
07415400 → ACNP
Volume
68
Issue
1
Year of publication
2000
Pages
81 - 86
Database
ISI
SICI code
0741-5400(200007)68:1<81:TCLOMR>2.0.ZU;2-R
Abstract
Activated T cells lyse the murine renal cancer Renca. We have examined the mechanism of tumor cell lysis with the use of T tells derived from C57BL/6, BALB/c, B6.gld, and B6.Pfp(-/-) mice, C57BL/6 and BALB/c T cells can lyse Renca cells through the use of both granule- and Fas Ligand (FasL)-mediated pathways. However, B6.gld T cells predominantly use granule-mediated killi ng, whereas B6.Pfp(-/-) T cells use Fast. The lysis of Renca by Pfp(-/-) T cells is only partially inhibited by the caspase inhibitor ZVAD-FMK, sugges ting that caspase-independent signaling is also important for Renca cell ly sis, When the reactive oxygen scavenger butylated hydroxyanisole was used a lone or hi combination with ZVAD-FMK a substantial reduction of Renca lysis was observed. Therefore, the caspase-independent generation of reactive ox ygen intermediates in Renca after Fas triggering contributes to the lysis o f these cells.