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Comparative proteomic analysis of renal proteins from IgA nephropathy model mice and control mice
by
Miyakawa Rena
, Suzuki, Takehiro
, Takahashi, Naoto
, Matsuda Yuka
, Matsumura Hirotoshi
, Sato Akiko
, Dohmae Naoshi
, Odaka Masafumi
, Komatsuda Atsushi
, Wakui Hideki
, Saito Ayano
, Abe Fumito
in
Animal models
/ IgA nephropathy
/ Immunoglobulin A
/ Kidney diseases
/ Liquid chromatography
/ Mass spectroscopy
/ Plasma cells
/ Proteins
2020
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Comparative proteomic analysis of renal proteins from IgA nephropathy model mice and control mice
by
Miyakawa Rena
, Suzuki, Takehiro
, Takahashi, Naoto
, Matsuda Yuka
, Matsumura Hirotoshi
, Sato Akiko
, Dohmae Naoshi
, Odaka Masafumi
, Komatsuda Atsushi
, Wakui Hideki
, Saito Ayano
, Abe Fumito
in
Animal models
/ IgA nephropathy
/ Immunoglobulin A
/ Kidney diseases
/ Liquid chromatography
/ Mass spectroscopy
/ Plasma cells
/ Proteins
2020
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
Comparative proteomic analysis of renal proteins from IgA nephropathy model mice and control mice
by
Miyakawa Rena
, Suzuki, Takehiro
, Takahashi, Naoto
, Matsuda Yuka
, Matsumura Hirotoshi
, Sato Akiko
, Dohmae Naoshi
, Odaka Masafumi
, Komatsuda Atsushi
, Wakui Hideki
, Saito Ayano
, Abe Fumito
in
Animal models
/ IgA nephropathy
/ Immunoglobulin A
/ Kidney diseases
/ Liquid chromatography
/ Mass spectroscopy
/ Plasma cells
/ Proteins
2020
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Comparative proteomic analysis of renal proteins from IgA nephropathy model mice and control mice
Journal Article
Comparative proteomic analysis of renal proteins from IgA nephropathy model mice and control mice
2020
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Overview
BackgroundHigh-IgA ddY (HIGA) mice, an animal model of human IgA nephropathy (IgAN), spontaneously develop nephropathy with glomerular IgA deposition and markedly elevated serum IgA levels from 25 weeks of age.MethodsWe performed a comparative proteomic analysis of the renal proteins collected from HIGA mice and control C57BL/6 mice at 5 or 38 weeks of age (the H5, H38, C5, and C38 groups) (n = 4 in each group). Proteins were extracted from the left whole kidney of each mouse and analyzed using nano-liquid chromatography–tandem mass spectrometry. The right kidneys were used for histopathological examinations.ResultsImmunohistochemical examinations showed glomerular deposition of IgA and the immunoglobulin joining (J) chain, and increased numbers of interstitial IgA- and J-chain-positive plasma cells in the H38 group. In the proteomic analysis, > 5000 proteins were identified, and 33 proteins with H38/H5 ratios of > 5.0, H38/C38 ratios of > 5.0, and C38/C5 ratios of < 1.5 were selected. Among them, there were various proteins that are known to be involved in human IgAN and/or animal IgAN models. Immunohistochemical examinations validated the proteomic results for some proteins. Furthermore, two proteins that are known to be associated with kidney disease displayed downregulated expression (H38/H5 ratio: 0.01) in the H38 group.ConclusionsThe results of comparative proteomic analysis of renal proteins were consistent with previous histopathological and serological findings obtained in ddY and HIGA mice. Various proteins that are known to be involved in kidney disease, including IgAN, and potential disease marker proteins exhibited markedly altered levels in HIGA mice.
Publisher
Springer Nature B.V
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