Renal proteome in mice with different susceptibilities to fluorosis.
Renal proteome in mice with different susceptibilities to fluorosis.
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DOI:
10.1371/journal.pone.0053261
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发表时间:
2013
期刊:
影响因子:
3.7
通讯作者:
Buzalaf MA
中科院分区:
文献类型:
--
作者:
Carvalho JG;Leite Ade L;Peres-Buzalaf C;Salvato F;Labate CA;Everett ET;Whitford GM;Buzalaf MA
A/J and 129P3/J mouse strains have different susceptibilities to dental fluorosis due to their genetic backgrounds. They also differ with respect to several features of fluoride (F) metabolism and metabolic handling of water. This study was done to determine whether differences in F metabolism could be explained by diversities in the profile of protein expression in kidneys. Weanling, male A/J mice (susceptible to dental fluorosis, n = 18) and 129P3/J mice (resistant, n = 18) were housed in pairs and assigned to three groups given low-F food and drinking water containing 0, 10 or 50 ppm [F] for 7 weeks. Renal proteome profiles were examined using 2D-PAGE and LC-MS/MS. Quantitative intensity analysis detected between A/J and 129P3/J strains 122, 126 and 134 spots differentially expressed in the groups receiving 0, 10 and 50 ppmF, respectively. From these, 25, 30 and 32, respectively, were successfully identified. Most of the proteins were related to metabolic and cellular processes, followed by response to stimuli, development and regulation of cellular processes. In F-treated groups, PDZK-1, a protein involved in the regulation of renal tubular reabsorption capacity was down-modulated in the kidney of 129P3/J mice. A/J and 129P3/J mice exhibited 11 and 3 exclusive proteins, respectively, regardless of F exposure. In conclusion, proteomic analysis was able to identify proteins potentially involved in metabolic handling of F and water that are differentially expressed or even not expressed in the strains evaluated. This can contribute to understanding the molecular mechanisms underlying genetic susceptibility to dental fluorosis, by indicating key-proteins that should be better addressed in future studies.
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DOI:
10.2170/jjphysiol.51.371
发表时间:
2001-06-01
期刊:
JAPANESE JOURNAL OF PHYSIOLOGY
影响因子:
--
作者:
Mori, Y;Kawasaki, A;Kubota, T
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Zou F
影响因子:
7.6
作者:
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通讯作者:
Stookey, GK
DOI:
10.1152/ajprenal.00182.2009
发表时间:
2010-03-01
影响因子:
4.2
作者:
Dynia, Diane W.;Steinmetz, Amy G.;Kocinsky, Hetal S.
通讯作者:
Kocinsky, Hetal S.
DOI:
10.1152/ajprenal.1995.269.5.f673
发表时间:
1995-11-01
期刊:
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY
影响因子:
--
作者:
LI, DL;APERIA, A;MEISTER, B
通讯作者:
MEISTER, B