Cargando…

Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium

BACKGROUND: To characterize changes in global protein expression in kidneys of transgenic rats overexpressing human selenoprotein M (SelM) in response to increased bioabivility of selenium (Sel), total proteins extracted from kidneys of 10-week-old CMV/hSelM Tg and wild-type rats were separated by 2...

Descripción completa

Detalles Bibliográficos
Autores principales: Goo, Jun Seo, Kim, Yo Na, Choi, Kyung Mi, Hwang, In Sik, Kim, Ji Eun, Lee, Young Ju, Kwak, Moon Hwa, Shim, Sun Bo, Jee, Seung Wan, Lim, Chul Joo, Seong, Je Kyung, Hwang, Dae Youn
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751301/
https://www.ncbi.nlm.nih.gov/pubmed/23937859
http://dx.doi.org/10.1186/1559-0275-10-10
_version_ 1782281571988930560
author Goo, Jun Seo
Kim, Yo Na
Choi, Kyung Mi
Hwang, In Sik
Kim, Ji Eun
Lee, Young Ju
Kwak, Moon Hwa
Shim, Sun Bo
Jee, Seung Wan
Lim, Chul Joo
Seong, Je Kyung
Hwang, Dae Youn
author_facet Goo, Jun Seo
Kim, Yo Na
Choi, Kyung Mi
Hwang, In Sik
Kim, Ji Eun
Lee, Young Ju
Kwak, Moon Hwa
Shim, Sun Bo
Jee, Seung Wan
Lim, Chul Joo
Seong, Je Kyung
Hwang, Dae Youn
author_sort Goo, Jun Seo
collection PubMed
description BACKGROUND: To characterize changes in global protein expression in kidneys of transgenic rats overexpressing human selenoprotein M (SelM) in response to increased bioabivility of selenium (Sel), total proteins extracted from kidneys of 10-week-old CMV/hSelM Tg and wild-type rats were separated by 2-dimensional gel electrophoresis and measured for changes in expression. RESULTS: Ten and three proteins showing high antioxidant enzymatic activity were up- and down-regulated, respectively, in SelM-overexpressing CMV/hSelM Tg rats compared to controls based on an arbitrary 2-fold difference. Up-regulated proteins included LAP3, BAIAP2L1, CRP2, CD73 antigen, PDGF D, KIAA143 homolog, PRPPS-AP2, ZFP313, HSP-60, and N-WASP, whereas down-regulated proteins included ALKDH3, rMCP-3, and STC-1. After Sel treatment, five of the up-regulated proteins were significantly increased in expression in wild-type rats, whereas there were no changes in CMV/hSelM Tg rats. Only two of the down-regulated proteins showed reduced expression in wild-type and Tg rats after Sel treatment. CONCLUSIONS: These results show the primary novel biological evidences that new functional protein groups and individual proteins in kidneys of Tg rats relate to Sel biology including the response to Sel treatment and SelM expression.
format Online
Article
Text
id pubmed-3751301
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-37513012013-08-27 Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium Goo, Jun Seo Kim, Yo Na Choi, Kyung Mi Hwang, In Sik Kim, Ji Eun Lee, Young Ju Kwak, Moon Hwa Shim, Sun Bo Jee, Seung Wan Lim, Chul Joo Seong, Je Kyung Hwang, Dae Youn Clin Proteomics Research BACKGROUND: To characterize changes in global protein expression in kidneys of transgenic rats overexpressing human selenoprotein M (SelM) in response to increased bioabivility of selenium (Sel), total proteins extracted from kidneys of 10-week-old CMV/hSelM Tg and wild-type rats were separated by 2-dimensional gel electrophoresis and measured for changes in expression. RESULTS: Ten and three proteins showing high antioxidant enzymatic activity were up- and down-regulated, respectively, in SelM-overexpressing CMV/hSelM Tg rats compared to controls based on an arbitrary 2-fold difference. Up-regulated proteins included LAP3, BAIAP2L1, CRP2, CD73 antigen, PDGF D, KIAA143 homolog, PRPPS-AP2, ZFP313, HSP-60, and N-WASP, whereas down-regulated proteins included ALKDH3, rMCP-3, and STC-1. After Sel treatment, five of the up-regulated proteins were significantly increased in expression in wild-type rats, whereas there were no changes in CMV/hSelM Tg rats. Only two of the down-regulated proteins showed reduced expression in wild-type and Tg rats after Sel treatment. CONCLUSIONS: These results show the primary novel biological evidences that new functional protein groups and individual proteins in kidneys of Tg rats relate to Sel biology including the response to Sel treatment and SelM expression. Springer 2013-08-12 /pmc/articles/PMC3751301/ /pubmed/23937859 http://dx.doi.org/10.1186/1559-0275-10-10 Text en Copyright ©2013 Goo et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Goo, Jun Seo
Kim, Yo Na
Choi, Kyung Mi
Hwang, In Sik
Kim, Ji Eun
Lee, Young Ju
Kwak, Moon Hwa
Shim, Sun Bo
Jee, Seung Wan
Lim, Chul Joo
Seong, Je Kyung
Hwang, Dae Youn
Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title_full Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title_fullStr Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title_full_unstemmed Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title_short Proteomic analysis of kidneys from selenoprotein M transgenic rats in response to increased bioability of selenium
title_sort proteomic analysis of kidneys from selenoprotein m transgenic rats in response to increased bioability of selenium
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3751301/
https://www.ncbi.nlm.nih.gov/pubmed/23937859
http://dx.doi.org/10.1186/1559-0275-10-10
work_keys_str_mv AT goojunseo proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT kimyona proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT choikyungmi proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT hwanginsik proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT kimjieun proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT leeyoungju proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT kwakmoonhwa proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT shimsunbo proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT jeeseungwan proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT limchuljoo proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT seongjekyung proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium
AT hwangdaeyoun proteomicanalysisofkidneysfromselenoproteinmtransgenicratsinresponsetoincreasedbioabilityofselenium