A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4
We synthesized unmodified Fe3O4 nanoparticles (NPs) with particles size from 10 nm to 100 nm. We cultured NRK-52E cell lines (rat, kidney) and treated with Fe3O4 NPs to investigate and evaluate the cytotoxicity of NPs for NRK-52E cells. Through global proteomics analysis using dimethyl labeling tech...
Saved in:
Main Authors: | , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
|
Series: | The Scientific World Journal |
Online Access: | http://dx.doi.org/10.1155/2014/754721 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832545537027473408 |
---|---|
author | Yi-Reng Lin Chao-Jen Kuo Hugo You-Hsien Lin Chin-Jen Wu Shih-Shin Liang |
author_facet | Yi-Reng Lin Chao-Jen Kuo Hugo You-Hsien Lin Chin-Jen Wu Shih-Shin Liang |
author_sort | Yi-Reng Lin |
collection | DOAJ |
description | We synthesized unmodified Fe3O4 nanoparticles (NPs) with particles size from 10 nm to 100 nm. We cultured NRK-52E cell lines (rat, kidney) and treated with Fe3O4 NPs to investigate and evaluate the cytotoxicity of NPs for NRK-52E cells. Through global proteomics analysis using dimethyl labeling techniques and liquid phase chromatography coupled with a tandem mass spectrometer (LC-MS/MS), we characterized 435 proteins including the programmed cell death related proteins, ras-related proteins, glutathione related proteins, and the chaperone proteins such as heat shock proteins, serpin H1, protein disulfide-isomerase A4, endoplasmin, and endoplasmic reticulum resident proteins. From the statistical data of identified proteins, we believed that NPs treatment causes cell death and promotes expression of ras-related proteins. In order to avoid apoptosis, NRK-52E cell lines induce a series of protective effects such as glutathione related proteins to reduce reactive oxygen species (ROS), and chaperone proteins to recycle damaged proteins. We suggested that, in the indigenous cellular environment, Fe3O4 NPs treatment induced an antagonistic effect for cell lines to go to which avoids apoptosis. |
format | Article |
id | doaj-art-b98f69117e59437c82f460e0bd392ceb |
institution | Kabale University |
issn | 2356-6140 1537-744X |
language | English |
publishDate | 2014-01-01 |
publisher | Wiley |
record_format | Article |
series | The Scientific World Journal |
spelling | doaj-art-b98f69117e59437c82f460e0bd392ceb2025-02-03T07:25:40ZengWileyThe Scientific World Journal2356-61401537-744X2014-01-01201410.1155/2014/754721754721A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4Yi-Reng Lin0Chao-Jen Kuo1Hugo You-Hsien Lin2Chin-Jen Wu3Shih-Shin Liang4Department of Biotechnology, Fooyin University, 151 Jinxue Road, Kaohsiung 83102, TaiwanGraduate Institute of Medicine, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 80708, TaiwanGraduate Institute of Medicine, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 80708, TaiwanKaiser Pharmaceutical Co., Ltd., 9 Huan-Gong Road, Tainan 71041, TaiwanDepartment of Biotechnology, College of Life Science, Kaohsiung Medical University, 100 Shih-Chuan 1st Road, Kaohsiung 80708, TaiwanWe synthesized unmodified Fe3O4 nanoparticles (NPs) with particles size from 10 nm to 100 nm. We cultured NRK-52E cell lines (rat, kidney) and treated with Fe3O4 NPs to investigate and evaluate the cytotoxicity of NPs for NRK-52E cells. Through global proteomics analysis using dimethyl labeling techniques and liquid phase chromatography coupled with a tandem mass spectrometer (LC-MS/MS), we characterized 435 proteins including the programmed cell death related proteins, ras-related proteins, glutathione related proteins, and the chaperone proteins such as heat shock proteins, serpin H1, protein disulfide-isomerase A4, endoplasmin, and endoplasmic reticulum resident proteins. From the statistical data of identified proteins, we believed that NPs treatment causes cell death and promotes expression of ras-related proteins. In order to avoid apoptosis, NRK-52E cell lines induce a series of protective effects such as glutathione related proteins to reduce reactive oxygen species (ROS), and chaperone proteins to recycle damaged proteins. We suggested that, in the indigenous cellular environment, Fe3O4 NPs treatment induced an antagonistic effect for cell lines to go to which avoids apoptosis.http://dx.doi.org/10.1155/2014/754721 |
spellingShingle | Yi-Reng Lin Chao-Jen Kuo Hugo You-Hsien Lin Chin-Jen Wu Shih-Shin Liang A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 The Scientific World Journal |
title | A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 |
title_full | A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 |
title_fullStr | A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 |
title_full_unstemmed | A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 |
title_short | A Proteomics Analysis to Evaluate Cytotoxicity in NRK-52E Cells Caused by Unmodified Nano-Fe3O4 |
title_sort | proteomics analysis to evaluate cytotoxicity in nrk 52e cells caused by unmodified nano fe3o4 |
url | http://dx.doi.org/10.1155/2014/754721 |
work_keys_str_mv | AT yirenglin aproteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT chaojenkuo aproteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT hugoyouhsienlin aproteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT chinjenwu aproteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT shihshinliang aproteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT yirenglin proteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT chaojenkuo proteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT hugoyouhsienlin proteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT chinjenwu proteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 AT shihshinliang proteomicsanalysistoevaluatecytotoxicityinnrk52ecellscausedbyunmodifiednanofe3o4 |