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
相关论文
共 50 条
  • [1] Using SILAC proteomics to investigate the effect of the mycotoxin, alternariol, in the human H295R steroidogenesis model
    Shewit Kalayou
    Anne Grethe Hamre
    Doreen Ndossi
    Lisa Connolly
    Morten Sørlie
    Erik Ropstad
    Steven Verhaegen
    Cell Biology and Toxicology, 2014, 30 : 361 - 376
  • [2] Relative quantification of the proteomic changes associated with the mycotoxin zearalenone in the H295R steroidogenesis model
    Busk, Oyvind L.
    Ndossi, Doreen
    Verhaegen, Steven
    Connolly, Lisa
    Eriksen, Gunnar
    Ropstad, Erik
    Sorlie, Morten
    TOXICON, 2011, 58 (6-7) : 533 - 542
  • [3] Bisphenol A Disrupts Steroidogenesis in Human H295R Cells
    Zhang, Xiaowei
    Chang, Hong
    Wiseman, Steve
    He, Yuhe
    Higley, Eric
    Jones, Paul
    Wong, Chris K. C.
    Al-Khedhairy, Abdulaziz
    Giesy, John P.
    Hecker, Markus
    TOXICOLOGICAL SCIENCES, 2011, 121 (02) : 320 - 327
  • [4] Effect of phthalate esters and alkylphenols on steroidogenesis in human adrenocortical H295R cells
    Nakajin, S
    Shinoda, S
    Ohno, S
    Nakazawa, H
    Makino, T
    ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY, 2001, 10 (03) : 103 - 110
  • [5] Evaluation of triclosan in the Hershberger and H295R steroidogenesis assays
    Farmer, W. T.
    Louis, G. W.
    Buckalew, A. R.
    Hallinger, D. R.
    Stoker, T. E.
    TOXICOLOGY LETTERS, 2018, 291 : 194 - 199
  • [6] Understanding the Effects of Atrazine on Steroidogenesis in the Human h295r and Rat Granulosa Cells
    Tinto, Nicole
    Hotchkiss, Michelle
    Buckalew, Angela
    Laws, Susan
    BIOLOGY OF REPRODUCTION, 2009, : 194 - 194
  • [7] THE EFFECT OF VALPROATE AND LEVETIRACETAM ON STEROIDOGENESIS IN FORSKOLIN-STIMULATED H295R CELLS
    von Krogh, Kristine
    Harjen, H.
    Almas, C.
    Zimmer, K.
    Dahl, E.
    Olsaker, I.
    Tauboll, E.
    Ropstad, E.
    Verhaegen, S.
    EPILEPSIA, 2009, 50 : 252 - 252
  • [8] The effect of valproate and levetiracetam on steroidogenesis in forskolin-stimulated H295R cells
    von Krogh, Kristine
    Harjen, Hannah
    Almas, Camilla
    Zimmer, Karin E.
    Dahl, Ellen
    Olsaker, Ingrid
    Tauboll, Erik
    Ropstad, Erik
    Verhaegen, Steven
    EPILEPSIA, 2010, 51 (11) : 2280 - 2288
  • [9] DIFFERENTIAL EFFECTS OF ANTIEPILEPTIC DRUGS ON HORMONE PRODUCTION IN H295R, A HUMAN IN VITRO MODEL FOR ADRENAL STEROIDOGENESIS
    Gustavsen, Marte W.
    Zimmer, K.
    Dahl, E.
    Olsaker, I.
    Ropstad, E.
    Tauboll, E.
    Verhaegen, Steven
    EPILEPSIA, 2008, 49 : 99 - 100
  • [10] Evaluating H295R steroidogenesis assay data for robust interpretation
    Tinwell, H.
    Karmaus, A.
    Gaskell, V.
    Gomes, C.
    Grant, C.
    Holmes, T.
    Jonas, A.
    Kellum, S.
    Krueger, K.
    Malley, L.
    Melching-Kollmuss, S.
    Mercier, O.
    Pandya, H.
    Placke, T.
    Settivari, R.
    De Waen, B.
    REGULATORY TOXICOLOGY AND PHARMACOLOGY, 2023, 143