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Integrated Transcriptional and Proteomic Analysis of Growth Hormone Suppression Mediated by Trichothecene T-2 Toxin in Rat GH3 Cells
D. Wan, X. Wang, Q. Wu, P. Lin, Y. Pan, A. Sattar, L. Huang, I. Ahmad, Y. Zhang, Z. Yuan,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Free Medical Journals
from 1996 to 1 year ago
Open Access Digital Library
from 1996-01-01
Medline Complete (EBSCOhost)
from 1998-01-01 to 1 year ago
PubMed
26141394
DOI
10.1093/toxsci/kfv131
Knihovny.cz E-resources
- MeSH
- Amino Acyl-tRNA Synthetases antagonists & inhibitors MeSH
- Apoptosis drug effects MeSH
- Cell Line MeSH
- Transcription, Genetic drug effects MeSH
- Peptide Initiation Factors antagonists & inhibitors MeSH
- eIF-2 Kinase antagonists & inhibitors MeSH
- Rats MeSH
- Oxidoreductases antagonists & inhibitors MeSH
- Protein Disulfide-Isomerases antagonists & inhibitors MeSH
- HSP90 Heat-Shock Proteins antagonists & inhibitors MeSH
- RNA-Binding Proteins antagonists & inhibitors MeSH
- Proteomics * MeSH
- Protein Biosynthesis drug effects MeSH
- RNA Interference drug effects MeSH
- Growth Hormone antagonists & inhibitors MeSH
- Gene Expression Profiling * MeSH
- T-2 Toxin analogs & derivatives pharmacology MeSH
- Cell Survival drug effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Chronic exposure to trichothecenes is known to disturb insulin-like growth factor 1 and signaling of insulin and leptin hormones and causes considerable growth retardation in animals. However, limited information was available on mechanisms underlying trichothecene-induced growth retardation. In this study, we employed an integrated transcriptomics, proteomics, and RNA interference (RNAi) approach to study the molecular mechanisms underlying trichothecene cytotoxicity in rat pituitary adenoma GH3 cells. Our results showed that trichothecenes suppressed the synthesis of growth hormone 1 (Gh1) and inhibited the eukaryotic transcription and translation initiation by suppressing aminoacyl-tRNA synthetases transcription, inducing eukaryotic translation initiation factor 2-alpha kinase 2 (EIF2AK2) and reducing eukaryotic translation initiation factor 5 a. The sulfhydryl oxidases , protein disulfide isomerase,and heat shock protein 90 (were greatly reduced, which resulted in adverse regulation of protein processing and folding. Differential genes and proteins associated with a decline in energy metabolism and cell cycle arrest were also found in our study. However, use of RNAi to interfere with hemopoietic cell kinase (Hck) and EIF2AK2 transcriptions or use of chemical inhibitors of MAPK, p38, Ras, and JNK partially reversed the reduction of Gh1 levels induced by trichothecenes. It indicated that the activation of MAPKs, Hck, and EIF2AK2 were important for trichothecene-induced growth hormone suppression. Considering the potential hazards of exposure to trichothecenes, our findings could help to improve our understanding regarding human and animal health implications.
College of Life Science Yangtze University Jingzhou Hubei China
Hubei Collaborative Innovation Center for Animal Nutrition and Feed Safety Wuhan Hubei China
References provided by Crossref.org
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