Differential thioredoxin reductase activity from human normal hepatic and hepatoma cell lines
- Authors
- Jung, HI; Lim, HW; Kim, BC; Park, EH; Lim, CJ
- Issue Date
- Apr-2004
- Publisher
- YONSEI UNIV COLL MEDICINE
- Keywords
- Chang; HepG2; human liver cell line; nitric oxide; oxidative stress; regulation; thioredoxin reductase
- Citation
- YONSEI MEDICAL JOURNAL, v.45, no.2, pp 263 - 272
- Pages
- 10
- Journal Title
- YONSEI MEDICAL JOURNAL
- Volume
- 45
- Number
- 2
- Start Page
- 263
- End Page
- 272
- URI
- https://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/15887
- DOI
- 10.3349/ymj.2004.45.2.263
- ISSN
- 0513-5796
1976-2437
- Abstract
- Thioredoxin reductase (TrxR), a component of the thioredoxin system, including thioredoxin (Trx) and NADPH, catalyzes the transfer of electrons from NADPH to Trx, acts as a reductant of disulfide-containing proteins and participates in the defense system against oxidative stresses. In this study, the regulation pattern of TrxR in the presence of various stressful reagents was compared between Chang (human normal hepatic cell) and HepG2 (human hepatoma cell) cell lines. Aluminum chloride (0.5 mM) and zinc chloride (0.5 mM) enhanced the TrxR activity in the Chang cell line to a higher degree than in the HepG2 cell line, but cupfic chloride (0.2 mM) and cadmium chloride (0.1 mM) enhanced the TrxR activity in the HepG2 cell line to a greater degree. The TrxR activities in both Chang and HepG2 cell lines were similarly induced by treatment with sodium selenite (0.02 mM) and menadione (0.5 and 1.0 mM). Lipopolysaccharide (2 mug/m1) increased the TrxR activity upto 4.02- and 2.2-fold in the Chang and HepG2 cell lines, respectively, in time-dependent manners. Hydrogen peroxide (5 mM) markedly enhanced the TrxR activity in the HepG2 cell line, but not in the Chang cell line. NO-generating sodium nitroprusside (3.0 and 6.0 mM) induced TrxR activities in both human liver cell lines. The TrxR activity was also induced in human liver cells under limited growth conditions by serum deprivation. These results imply that the TrxR activities in normal hepatic and hepatoma cell lines are subject to different regulatory responses to various stresses.
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