Qualitative and quantitative differences in the intensity of Fas-mediated intracellular signals determine life and death in T cells

Min Jung Shin, Jae Hyuck Shim, Jae Young Lee, Wook Jin Chae, Heung Kyu Lee, Tomohiro Morio, Jun Han Park, Eun Ju Chang, Sang Kyou Lee

Research output: Contribution to journalArticlepeer-review

2 Citations (Scopus)


Fas stimulation has been reported to promote the activation and proliferation of T lymphocytes, but the intracellular signalling pathways that mediate non-apoptotic responses to Fas are poorly defined. To distinguish between the activation signalling and the death-inducing pathway downstream of Fas, we generated a novel T cell line expressing a chimeric hCD8-FasC protein and found that stimulation with the anti-CD8 antibodies induced tyrosine phosphorylation of TCR-proximal proteins, activation of Raf-1/ERK, p38 and JNK, and increased expression of CD69, Fas, and Fas ligand. Stimulation of hCD8-FasC-induced activation of an atypical NF-κB pathway, partial cleavage of caspases, and increased expression of TRAF1, FLIPL and FLIPS, thereby protecting T cells from FasL-mediated apoptosis. The proliferative response transmitted through hCD8-FasC chimeric receptors was converted into death signals when cells were stimulated, resulting in increased expression of IL-2 and Nur77 and increased caspase cleavage. Surprisingly, both the enhanced expression of FLIPL and FLIPS and the complete inhibition of FLIPS expression were functionally associated with cell death induction. These findings imply that Fas is able to trigger intracellular signalling events driving both apoptosis and activation of T cells but that cell fate is determined by quantitative and qualitative differences in intracellular signalling following Fas stimulation.

Original languageEnglish
Pages (from-to)262-270
Number of pages9
JournalInternational Journal of Hematology
Issue number2
Publication statusPublished - 2010 Sept

Bibliographical note

Funding Information:
Acknowledgments This work was supported in part by Creative Research Initiatives, a National Research Foundation of Korea Grant funded by the Korean Government (2010-0000733) and the Brain Korea 21 (BK21) Program to S. K. Lee.

All Science Journal Classification (ASJC) codes

  • Hematology


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