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Clinical and Diagnostic Laboratory Immunology, July 2001, p. 837-840, Vol. 8, No. 4
Department of Microbiology, Ajou University
School of Medicine, Suwon 442-749,1
Department of Clinical Pathology, College of Shinheung,
Uejongbu 480-701,2 Department of
Biology, College of Natural Science, Kyung-Hee University, Seoul
130-701,3 and Department of
Parasitology, Yonsei University, College of Medicine, Seoul
121-752,4 Korea
Received 22 December 2000/Returned for modification 13 April
2001/Accepted 2 May 2001
To determine whether pathogenic Acanthamoeba
culbertsoni trophozoites and lysate can induce cytopathic changes
in primary-culture microglial cells, morphological changes were
observed by transmission electron microscopy (TEM). In addition, the
secretion of two kinds of cytokines, tumor necrosis factor alpha
(TNF-
1071-412X/01/$04.00+0 DOI: 10.1128/CDLI.8.4.837-840.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Cytopathic Changes in Rat Microglial Cells Induced
by Pathogenic Acanthamoeba culbertsoni: Morphology and
Cytokine Release
) and interleukin-1
(IL-1
), from microglial cells was
observed. Trophozoites of pathogenic A. culbertsoni made
contact with microglial cells and produced digipodia. TEM revealed that
microglial cells cocultured with amoebic trophozoites underwent a
necrotic process, accompanied by lysis of the cell membrane. TEM of
microglial cells cocultured with amoebic lysate showed that the
membranes of the small cytoplasmic vacuoles as well as the cell
membrane were lysed. The amounts of TNF-
secreted from microglial
cells cocultured with A. culbertsoni trophozoites or lysate
increased at 6 h of incubation. The amounts of IL-1
secreted
from microglial cells cocultured with A. culbertsoni trophozoites at 6 h of incubation was similar to those secreted from the control group, but the amounts decreased during cultivation with A. culbertsoni lysate. These results suggest that
pathogenic A. culbertsoni induces the cytopathic effects in
primary-culture rat microglial cells, with the effects characterized by
necrosis of microglial cells and changes in levels of secretion of
TNF-
and IL-1
from microglial cells.
*
Corresponding author. Mailing address: Department of
Microbiology, Ajou University School of Medicine, Suwon 442-749, Korea. Phone: (82) 31-219-5076. Fax: (82) 32-219-5079. E-mail:
hjshin{at}madang.ajou.ac.kr.
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