Published July 15, 2013 | Version v1
Journal article

Hypoxia inducible factor-1 (HIF-1)–flavin containing monooxygenase-2 (FMO-2) signaling acts in silver nanoparticles and silver ion toxicity in the nematode, Caenorhabditis elegans

  • 1. School of Environmental Engineering and Graduate School of Energy and Environmental System Engineering, University of Seoul, 90 Jeonnong-dong, Dongdaemun-gu, Seoul 130-743 (Korea, Republic of)
  • 2. Department of Chemical Engineering, Kwangwoon University, 447-1, Wolgye-dong, Nowon-gu, Seoul 139-701 (Korea, Republic of)

Description

In the present study, nanotoxicity mechanism associated with silver nanoparticles (AgNPs) exposure was investigated on the nematode, Caenorhabditis elegans focusing on the hypoxia response pathway. In order to test whether AgNPs-induced hypoxia inducible factor-1 (HIF-1) activation was due to hypoxia or to oxidative stress, depletion of dissolved oxygen (DO) in the test media and a rescue effect using an antioxidant were investigated, respectively. The results suggested that oxidative stress was involved in activation of the HIF-1 pathway. We then investigated the toxicological implications of HIF-1 activation by examining the HIF-1 mediated transcriptional response. Of the genes tested, increased expression of the flavin containing monooxygenase-2 (FMO-2) gene was found to be the most significant as induced by AgNPs exposure. We found that AgNPs exposure induced FMO-2 activation in a HIF-1 and p38 MAPK PMK-1 dependent manner, and oxidative stress was involved in it. We conducted all experiments to include comparison of AgNPs and AgNO3 in order to evaluate whether any observed toxicity was due to dissolution or particle specific. The AgNPs and AgNO3 did not produce any qualitative differences in terms of exerting toxicity in the pathways observed in this study, however, considering equal amount of silver mass, in every endpoint tested the AgNPs were found to be more toxic than AgNO3. These results suggest that Ag nanotoxicity is dependent not only on dissolution of Ag ion but also on particle specific effects and HIF-1–FMO-2 pathway seems to be involved in it. - Highlights: • HIF-1 signaling was investigated in C. elegans exposed to AgNPs and AgNO3. • HIF-1 and PMK-1 were needed for AgNPs- and AgNO3-induced fmo-2 gene expression. • PMK-1–HIF-1–FMO-2 pathway was dependent on oxidative stress. • AgNPs and AgNO3 did not produce any qualitative differences in HIF-1 signaling. • AgNPs were more toxic than an equal amount of silver mass contained in AgNO3

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2013.03.028

Additional details

Identifiers

DOI
10.1016/j.taap.2013.03.028;
PII
S0041-008X(13)00137-3;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
270
Journal Issue
2
Journal Page Range
p. 106-113
ISSN
0041-008X
CODEN
TXAPA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45106763
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
ANOXIA; ANTIOXIDANTS; DISSOLVED GASES; NANOSTRUCTURES; NEMATODES; OXIDATION; SILVER IONS; SILVER NITRATES; STRESSES; TOXICITY
Descriptors DEC
ANIMALS; CHARGED PARTICLES; CHEMICAL REACTIONS; FLUIDS; GASES; INVERTEBRATES; IONS; NITRATES; NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; SILVER COMPOUNDS; SOLUTES; TRANSITION ELEMENT COMPOUNDS

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.