Using SILAC proteomics to investigate the effect of the mycotoxin, alternariol, in the human H295R steroidogenesis model

被引:10
|
作者
Kalayou, Shewit [1 ,2 ]
Hamre, Anne Grethe [3 ]
Ndossi, Doreen [1 ,4 ]
Connolly, Lisa [5 ]
Sorlie, Morten [3 ]
Ropstad, Erik [1 ]
Verhaegen, Steven [1 ]
机构
[1] Norwegian Sch Vet Sci, Oslo, Norway
[2] Mekelle Univ, Coll Vet Med, Mekelle, Ethiopia
[3] Norwegian Univ Life Sci, Dept Chem Biotechnol & Food Sci, N-1432 As, Norway
[4] Sokoine Univ Agr, Morogoro, Tanzania
[5] Queens Univ Belfast, Sch Biol Sci, Inst Agrifood & Land Use, Belfast, Antrim, North Ireland
关键词
Alternariol; Mycotoxins; SILAC; Steroidogenesis; Endocrine disruption; Quantitative proteomics; CELL-CYCLE; IDENTIFICATION; EXPRESSION; PROTEINS; TRANSLATION; ZEARALENONE; MODULATION; MEDIATOR; CULTURE; GENES;
D O I
10.1007/s10565-014-9290-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mycotoxin alternariol (AOH) is an important contaminant of fruits and cereal products. The current study sought to address the effect of a non-toxic AOH concentration on the proteome of the steroidogenic H295R cell model. Quantitative proteomics based on stable isotope labeling by amino acids in cell culture (SILAC) coupled to 1D-SDS-PAGE-LC-MS/MS was applied to subcellular-enriched protein samples. Gene ontology (GO) and ingenuity pathway analysis (IPA) were further carried out for functional annotation and identification of protein interaction networks. Furthermore, the effect of AOH on apoptosis and cell cycle distribution was also determined by the use of flow cytometry analysis. This work identified 22 proteins that were regulated significantly. The regulated proteins are those involved in early stages of steroid biosynthesis (SOAT1, NPC1, and ACBD5) and C21-steroid hormone metabolism (CYP21A2 and HSD3B1). In addition, several proteins known to play a role in cellular assembly, organization, protein synthesis, and cell cycle were regulated. These findings provide a new framework for studying the mechanisms by which AOH modulates steroidogenesis in H295R cell model.
引用
收藏
页码:361 / 376
页数:16
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