Exp Mol Med.  2003 Jun;35(3):211-221.

Phagocytosis of serum-and IgG-opsonized zymos an particles induces apoptosis through superoxide but not nitric oxide in macrophage J774A.1

Affiliations
  • 1Department of Biochmisry, College of Medicine, Hallym University, Chunchon 200-702, Korea. jbpark@hallym.ac.kr
  • 2Department of Physiology, College of Medicine, Hallym University, Chunchon 200-702, Korea.
  • 3Department of Microbiology, College of Medicine, Hallym University, Chunchon 200-702, Korea.
  • 4Ilsong Institute of Life Science, Hallym University Ilsong Building, Keanyang-dong 1605-4, Dongan-gu Anyang 431-060, Korea.

Abstract

Phagocytosis of serum- and IgG-opsonized zymosan (SOZ and IOZ, respectively) particles into J774A.1 macrophages induced apoptosis of the cells, accompanied by the expression of p21(WAF1), one of cyclin-dependent protein kinase (CDK) inhibitors. Furthermore, phagocytosis of SOZ and IOZ particles into macophages induced superoxide formation. Tat-superoxide dismutase (SOD), which is readily transduced into the cells using Tat-domain, protected the cells from the apoptosis induced by phagocytosis of SOZ and IOZ particles. lipopolysaccharide (LPS)/interferon-gamma (IFN-gamma) also caused the apoptosis of the cells. However, Tat-SOD could not protect the cells from LPS/IFN-gamma induced apoptosis, suggesting that apoptosis mechanisms involved are different from each other. In the present study, we determined the amounts of nitric oxide (NO) produced by SOZ, IOZ, and LPS/IFN-gamma, and found that SOZ and IOZ did not induce the generation of NO in macrophages, whereas LPS/ IFN-gamma did. The apoptosis due to phagocytosis was accompanied with the release of cytochrome c from mitochondrial membrane to cytosolic fraction. Furthermore, SOZ and IOZ induced the cleavage of procasapase-3 (35 kDa) to give rise to an active caspase-3 (20 kDa), which was blocked by Tat- SOD but not by 2-phenyl-4,4,5,5-tetramethylimidazoline-1-oxyl 3-oxide (PTIO), a scavenger of NO. On the other hand, LPS/IFN-gamma caused the activation of procaspase-3, which was blocked by PTIO but not by Tat-SOD. Taken together, phagocytosis of SOZ and IOZ particles induced apoptosis through superoxide but not NO in macrophages, accompanied with the release of cytochrome c and the activation of caspase-3.

Keyword

apoptosis; caspase-3; macrophages; nitricoxide; phagocytosis; superoxides; zymosan

MeSH Terms

Apoptosis/*immunology
Caspases/metabolism
Cell Line
Cyclins/biosynthesis
Cytochromes c/metabolism
Immunoglobulin G/*immunology
Interferon Type II/pharmacology
Lipopolysaccharides/pharmacology
Macrophages/*immunology/metabolism
Nitric Oxide/*metabolism
Opsonins/immunology
Phagocytosis/*physiology
Superoxide Dismutase/metabolism
Superoxides/*metabolism
Zymosan
Full Text Links
  • EMM
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr