Cell Death-Associated Translocation of Plasma Membrane Components Induced by CTL
Author(s) -
Yukishige Kawasaki,
Takako Saitô,
Yoshiko Shirota-Someya,
Yuko Ikegami,
Hajime Komano,
Mi-Heon Lee,
Christopher J. Froelich,
Nobukata Shinohara,
Hajime Takayama
Publication year - 2000
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.164.9.4641
Subject(s) - ctl* , chromosomal translocation , intracellular , microbiology and biotechnology , programmed cell death , apoptosis , perforin , cell , cell membrane , biology , membrane , clone (java method) , chemistry , cytotoxicity , biochemistry , cytotoxic t cell , in vitro , gene , dna
In the very early stages of target cell apoptosis induced by CTL, we found that fluorescence of labeling probes of the target plasma membrane, such as N-(3-triethylammoniumpropyl)-4-(p-dibutylaminostyryl)pyridin ium dibromide (FM1-43), was translocated into intracellular membrane structures including nuclear envelope and mitochondria. This translocation was associated with the execution of CTL-mediated killing, because neither the CTL-target conjugation alone nor the binding of noncytotoxic Th2 clone with target cell was sufficient to provoke the process. Although FM1-43 translocation was observed in perforin-mediated cytotoxicity, examinations with several other dyes failed to detect the evidence for membrane damages that may cause influx of the dye. Moreover, the translocation was also observed in Fas-dependent apoptosis. These data indicate that the translocation precedes the damage of plasma membrane and intracellular organella in the course of apoptotic cell death and may represent the existence of a membrane trafficking that mediates the translocation of plasma membrane components in the early onset of apoptotic cell death.
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