Mol. Cells 2010; 29(6): 585-594
Published online May 20, 2010
https://doi.org/10.1007/s10059-010-0073-4
© The Korean Society for Molecular and Cellular Biology
Correspondence to : *Correspondence: dkchung@khu.ac.kr
Lipoteichoic acid (LTA) from Staphylococcus aureus (aLTA) and from Lactobacillus plantarum LTA (pLTA) are both recognized by Toll-like receptor 2 (TLR2), but cause different stimulatory effects on the innate immune and inflammatory responses, and their underlying cellular mechanisms are unknown. In this study, comparative proteome analysis was performed using two-dimensional gel electrophoresis and mass spectrometry on protein extracts from human monocyte THP-1 cells stimulated with either aLTA or pLTA. Differentially expressed proteins might be involved in innate immunity and inflammation. Cells treated with aLTA and with pLTA showed different protein expression profiles. Of 60 identified proteins, 10 were present only in treated cells (8 in aLTA-treated only, and 2 in pLTA-treated only), 1 protein (IMPDH2) was suppressed by pLTA, and 49 were up- or down-regulated more than three-fold by aLTA- or pLTA- stimulation. Several proteins involved in immunity or inflammation, anti-oxidation, or RNA processing were significantly changed in expression by aLTA- or pLTA-stimulation, including cyclophilin A, HLA-B27, D-dopachrome tautomerase, Mn-SOD, hnRNP-C, PSF and KSRP. These data demonstrated that aLTA and pLTA had different effects on the protein profile of THP-1 cells. Comparison of the proteome alterations will provide candidate biomarkers for further investigation of the immunomodulatory effects of aLTA and pLTA, and the involvement of aLTA in the pathogenesis of Staphylococcus aureus sepsis.
Keywords 2-DE, gram-positive bacteria, lipoteichoic acid, proteome analysis, THP-1 cells
Mol. Cells 2010; 29(6): 585-594
Published online June 30, 2010 https://doi.org/10.1007/s10059-010-0073-4
Copyright © The Korean Society for Molecular and Cellular Biology.
Ri-Zhong Zeng1,2, Han Geun Kim1, Na Ra Kim1, Hae Young Lee1, Bong Jun Jung1, Mi Yeon Ko3,
Seung Yeon Lee3, and Dae Kyun Chung1,3,4,*
1School of Biotechnology and Institute of Life Science and Resources, Kyung Hee University, Yongin 449-701, Korea, 2Rubber Research Institute, Chinese Academy of Tropical Agriculture Sciences, P.R. China, 3Skin Biotechnology Center, Kyung Hee University, Yongin 449-701, Korea, 4RNA Inc., College of Life Science, Kyung Hee University, Yongin 449-701, Korea
Correspondence to:*Correspondence: dkchung@khu.ac.kr
Lipoteichoic acid (LTA) from Staphylococcus aureus (aLTA) and from Lactobacillus plantarum LTA (pLTA) are both recognized by Toll-like receptor 2 (TLR2), but cause different stimulatory effects on the innate immune and inflammatory responses, and their underlying cellular mechanisms are unknown. In this study, comparative proteome analysis was performed using two-dimensional gel electrophoresis and mass spectrometry on protein extracts from human monocyte THP-1 cells stimulated with either aLTA or pLTA. Differentially expressed proteins might be involved in innate immunity and inflammation. Cells treated with aLTA and with pLTA showed different protein expression profiles. Of 60 identified proteins, 10 were present only in treated cells (8 in aLTA-treated only, and 2 in pLTA-treated only), 1 protein (IMPDH2) was suppressed by pLTA, and 49 were up- or down-regulated more than three-fold by aLTA- or pLTA- stimulation. Several proteins involved in immunity or inflammation, anti-oxidation, or RNA processing were significantly changed in expression by aLTA- or pLTA-stimulation, including cyclophilin A, HLA-B27, D-dopachrome tautomerase, Mn-SOD, hnRNP-C, PSF and KSRP. These data demonstrated that aLTA and pLTA had different effects on the protein profile of THP-1 cells. Comparison of the proteome alterations will provide candidate biomarkers for further investigation of the immunomodulatory effects of aLTA and pLTA, and the involvement of aLTA in the pathogenesis of Staphylococcus aureus sepsis.
Keywords: 2-DE, gram-positive bacteria, lipoteichoic acid, proteome analysis, THP-1 cells
Si-Hyeon Um, Jin-Sik Kim, Saemee Song, Nam Ah Kim, Seong Hoon Jeong, and Nam-Chul Ha
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