skip to main content
OSTI.GOV title logo U.S. Department of Energy
Office of Scientific and Technical Information

Title: Simultaneous induction of apoptotic, autophagic, and necrosis-like cell death by monoclonal antibodies recognizing chicken transferrin receptor

Journal Article · · Biochemical and Biophysical Research Communications
;  [1];  [2];  [1];  [3];  [1]
  1. Cell Biology Laboratory, Department of Pharmaceutical Sciences, School of Pharmacy, Kinki University, 4-1 Kowakae 3-chome, Higashiosaka-shi, Osaka 577-8502 (Japan)
  2. Department of Oral Anatomy, Developmental Biology, Showa University School of Dentistry, 1-5-8 Hatanodai, Shinagawa-ku, Tokyo 142-8555 (Japan)
  3. Kyoritsu University of Pharmacy, 1-5-30 Shibakohen, Minato-ku, Tokyo 105-8512 (Japan)

Programmed cell death (PCD) is categorized as apoptotic, autophagic, or necrosis-like. Although the possibility that plural (two or three) death signals could be induced by a given stimulus has been reported, the precise mechanisms regulating PCD are not well understood. Recently, we have obtained two anti-chicken transferrin receptor (TfR) monoclonal antibodies (mAbs; D18 and D19) inducing a unique cell death. Although the cell death had several features of apoptosis, autophagic and necrosis-like morphological alterations were simultaneously observed in electron microphotographs. In addition to cells with condensed chromatin and an intact plasma membrane (apoptotic cells), cells having many vacuoles in the cytoplasm (autophagic cells), and enlarged cells with ruptured plasma membranes (necrosis-like cells) were observed in DT40 cells treated with the mAbs, however, the latter two types of dead cells were not detected upon treatment with staurosporine, a typical apoptosis inducer. In autophagic cells, numerous membrane-bound vesicles occupying most of the cytoplasmic space, which frequently contained electron-dense materials from cytoplasmic fragments and organelles, were observed. The simultaneous induction of multiple death signals from a stimulus via the TfR is of great interest to those researching cell death. In addition, activation of caspases was observed in DT40 cells treated with D19, however, the cell death was not inhibited with z-VAD-fmk, a pan-caspase inhibitor, suggesting that at least in part, a caspase-independent pathway is involved in the TfR-mediated cell death.

OSTI ID:
21043665
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 367, Issue 4; Other Information: DOI: 10.1016/j.bbrc.2008.01.030; PII: S0006-291X(08)00055-7; Copyright (c) 2008 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

Similar Records

Caspase-3 is required in the apoptotic disintegration of the nuclear matrix
Journal Article · Tue Nov 15 00:00:00 EST 2005 · Experimental Cell Research · OSTI ID:21043665

Oxaliplatin triggers necrosis as well as apoptosis in gastric cancer SGC-7901 cells
Journal Article · Fri May 01 00:00:00 EDT 2015 · Biochemical and Biophysical Research Communications · OSTI ID:21043665

Sodium fluoride induces apoptosis in mouse embryonic stem cells through ROS-dependent and caspase- and JNK-mediated pathways
Journal Article · Thu Mar 15 00:00:00 EDT 2012 · Toxicology and Applied Pharmacology · OSTI ID:21043665