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Changes in protein expression profiles in bovine endometrial epithelial cells exposed to E coli LPS challenge

Authors :
Gilles Charpigny
M. Chanrot
Luigi Bonizzi
Alessio Soggiu
Patrice Humblot
Cristian Piras
Andrea Urbani
Viviana Greco
Paola Roncada
Yongzhi Guo
Dipartimento di Medicina Veterinaria
Università degli studi di Milano [Milano]
Division of Reproduction, Department of Clinical Sciences
Swedish University of Agricultural Sciences (SLU)
Rajamangala University of Technology
Proteomics and Metabonomics Unit
IRCCS Santa Lucia Foundation
Istituto di Biochimica e Biochimica Clinica
Università Cattolica del Sacro Cuore
Biologie du développement et reproduction (BDR)
École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)
Istituto Sperimentale Italiano Lazzaro Spallanzani
Rajamangala University of Te chnology Srivijaya (RMUTSV, Thailand)
European Project: 311776
Dipartimento di Medicina Veterinaria (DIMEVET)
Università degli Studi di Milano [Milano] (UNIMI)
Università cattolica del Sacro Cuore [Milano] (Unicatt)
Biologie du Développement et Reproduction (BDR)
École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)
Istituto Spallanzani
Università degli Studi di Milano = University of Milan (UNIMI)
Rajamangala University of Technology Thanyaburi (RMUTT)
École nationale vétérinaire - Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)
Source :
Molecular BioSystems, Molecular BioSystems, 2017, 13 (2), pp.392-405. ⟨10.1039/c6mb00723f⟩, Molecular BioSystems 2 (13), 392-405. (2017)
Publication Year :
2017
Publisher :
HAL CCSD, 2017.

Abstract

E. coli is one of the most frequently involved bacteria in uterine diseases. Lipopolysaccharide (LPS) is a component of the outer membrane of Gram-negative bacteria involved in pathogenic processes leading to post-partum metritis and endometritis in cattle. It also causes inflammation of the endometrium. The increase of cell proliferation by LPS is part of the inflammatory process. The aim of this study was to investigate possible changes in protein expression in relation to the proliferative response of bEECs after challenge with E. coli-LPS. In vitro culture of bEECs was performed from cow genital tracts collected at a slaughterhouse. In passage 5, bEECs from each of 9 cows (3 series of 3 cows) were exposed to 0, 8, and 16 μg ml(-1) LPS for 72 h. At time 0 and 72 h later, attached cells/living cells were counted and for each time and LPS dosage, cells were frozen for proteomic analyses. All samples from the 3 series were analyzed by 2-D gel electrophoresis coupled to MALDI-TOF/TOF mass spectrometry. The samples from the first series were subjected to shotgun nLC-MS/MS analysis. From the whole differential proteomics analysis, 38 proteins were differentially expressed (p < 0.05 to p < 0.001) following exposure to LPS. Among them, twenty-eight were found to be up-regulated in the LPS groups in comparison to control groups and ten were down-regulated. Differentially expressed proteins were associated with cell proliferation and apoptosis, transcription, destabilization of cell structure, oxidative stress, regulation of histones, allergy and general cell metabolism pathways. The de-regulations induced by LPS were consistent with the proliferative phenotype and indicated strong alterations of several cell functions. In addition, some of the differentially expressed proteins relates to pathways activated at the time of implantation. The specific changes induced through those signals may have negative consequences for the establishment of pregnancy.

Details

Language :
English
ISSN :
17422051
Database :
OpenAIRE
Journal :
Molecular BioSystems, Molecular BioSystems, 2017, 13 (2), pp.392-405. ⟨10.1039/c6mb00723f⟩, Molecular BioSystems 2 (13), 392-405. (2017)
Accession number :
edsair.doi.dedup.....330cb1186de3385d783d2f9c859f19ec