Effect of Nitric Oxide and Peroxynitrite ( ONOO- ) on the Apoptosis of Murine Bladder Tumor-2 Cell Line.
- Author:
Hyun Chul PARK
1
;
Hun Taeg CHUNG
;
Joung Sik RIM
Author Information
1. Wonkwang University School of Medicine, Iksan, Korea.
- Publication Type:Original Article
- Keywords:
nitric oxide;
peroxynitrite;
MBT-2 cell line
- MeSH:
Apoptosis*;
Cell Death;
Cell Line*;
DNA Fragmentation;
Humans;
Immune System;
Macrophages;
Neutrophils;
Nitric Oxide Synthase;
Nitric Oxide*;
Peroxynitrous Acid*;
Superoxides;
Tissue Donors;
Urinary Bladder Neoplasms;
Urinary Bladder*;
Vasodilation
- From:Korean Journal of Urology
1997;38(2):120-128
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Nitric oxide (NO) has been emerged as an important intracellular and intercellular regulatory molecule having functions as diverse vasodilatation, neural communication, and host defense. In the immune system, NO produced by activated macrophage or neutrophil is known to kill tumor cells as a defense molecule. In addition, recent reports demonstrated that NO could interact with superoxide to generate peroxynitrite (ONOO-), an anion and a potent oxidant, in macrophages or other cellular systems. The production of peroxynitrite has been recognized to be associated with the activation and expression of inducible NO synthase (iNOS). In this study, to evaluate the role of NO and peroxynitrite in murine bladder tumor cells, the author investigate the effect of NO and peroxynitrite on the viability, cytotoxicity, and DNA fragmentation of MBT-2 cells. The results are as followings: 1. Activated macrophages treated with INF-r, LPS, or INF-r+ LPS showed increment of nitrite (NO2) production and cytotoxicity against MBT-2 cells in a dose dependent manner. However, treatment with NGMMA, a NOS inhibitor, decreased NO2- production and cytotoxicity. 2. Treatment with SNP, a nitric oxide donor, increased NO2 production and DNA fragmentation (%), but decreased viability (%) of MBT-2 cells in a concentration dependent manner. 3. Treatment with peroxynitrite increased cytotoxicity and DNA fragmentation, but decreased viability of MBT-2 cells in a concentration dependent manner. 4. NO- and peroxynitrite-mediated increment of cytotoxicity in MBT-2 cells was corresponded to the programmed cell death, apoptosis. Taken together, these data indicate that NO and peroxynitrite elaborated from macrophages or other cellular systems may increase the cytotoxicity of MBT-2 cells via the mechanism of apoptosis.
