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Infect. Immun., 01 1995, 259-263, Vol 63, No. 1
SM Rahman, MY Pu, H Yi, K Ohkusu, M Kato, K Isobe, R Taguchi, H Ikezawa and I Nakashima
Phosphatidylinositol-specific phospholipase C (PIPLC) from Bacillus
thuringiensis, which cleaves phosphatidylinositol or
glycosylphosphatidylinositol on the external cell surface to generate a
second messenger for intracellular signal transduction (S. Rahman et al.,
FEBS Lett. 303:193-196, 1992), was found to preferentially promote the
generation of alloantigen-specific cytotoxic T lymphocytes in mixed
leukocyte culture. PIPLC affected an early stage of cytotoxic T- lymphocyte
activation in culture, and there was no evidence of any soluble cellular
mediators of this PIPLC action. PIPLC neither enhanced overall cell
proliferation nor noticeably promoted interleukin-2 and -4 production in
mixed leukocyte culture. The relative population size of Ly-2+ T cells was
increased, however, in a late mixed leukocyte culture with PIPLC. In
addition, PIPLC enhanced an anti-CD3 monoclonal antibody- induced early
increase in [Ca2+]i. These results suggest a new parasite
(bacterium)-oriented mechanism for enhancing antigen-driven host cytotoxic
T-lymphocyte immunity which does not include promotion of interleukin-2
production.
Copyright © 1995, American Society for Microbiology
Promotion of cytotoxic T-cell generation in mixed leukocyte culture by phosphatidylinositol-specific phospholipase C from Bacillus thuringiensis
Department of Immunology, Nagoya University School of Medicine, Japan.
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