A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid

<p>Abstract</p> <p>Background</p> <p>Various animal models of renal failure have been produced and used to investigate mechanisms underlying renal disease and develop therapeutic drugs. Most methods available to produce such models appear to involve subtotal nephrectomy...

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Main Authors: Nakamura Shingo, Terashima Masuo, Kikuchi Natsuko, Kimura Minoru, Maehara Tadaaki, Saito Akira, Sato Masahiro
Format: Article
Language:English
Published: BMC 2004-04-01
Series:BMC Nephrology
Subjects:
Online Access:http://www.biomedcentral.com/1471-2369/5/4
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spelling doaj-2902813b645c4beda6743dce565ae3bd2020-11-24T23:29:04ZengBMCBMC Nephrology1471-23692004-04-0151410.1186/1471-2369-5-4A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmidNakamura ShingoTerashima MasuoKikuchi NatsukoKimura MinoruMaehara TadaakiSaito AkiraSato Masahiro<p>Abstract</p> <p>Background</p> <p>Various animal models of renal failure have been produced and used to investigate mechanisms underlying renal disease and develop therapeutic drugs. Most methods available to produce such models appear to involve subtotal nephrectomy or intravenous administration of antibodies raised against basement membrane of glomeruli. In this study, we developed a novel method to produce mouse models of renal failure by intravenous injection of a plasmid carrying a toxic gene such as diphtheria toxin A-chain (DT-A) gene. DT-A is known to kill cells by inhibiting protein synthesis.</p> <p>Methods</p> <p>An expression plasmid carrying the cytomegalovirus enhancer/chicken β-actin promoter linked to a DT-A gene was mixed with lipid (FuGENE™6) and the resulting complexes were intravenously injected into adult male B6C3F1 mice every day for up to 6 days. After final injection, the kidneys of these mice were sampled on day 4 and weeks 3 and 5.</p> <p>Results</p> <p>H-E staining of the kidney specimens sampled on day 4 revealed remarkable alterations in glomerular compartments, as exemplified by mesangial cell proliferation and formation of extensive deposits in glomerular basement membrane. At weeks 3 and 5, gradual recovery of these tissues was observed. These mice exhibited proteinuria and disease resembling sub-acute glomerulonephritis.</p> <p>Conclusions</p> <p>Repeated intravenous injections of DT-A expression plasmid DNA/lipid complex caused temporary abnormalities mainly in glomeruli of mouse kidney. The disease in these mice resembles sub-acute glomerulonephritis. These DT-A gene-incorporated mice will be useful as animal models in the fields of nephrology and regenerative medicine.</p> http://www.biomedcentral.com/1471-2369/5/4diphtheria toxinintravenous injectionplasmid/liposome complexrenal diseasecell ablationglomerulonephritis
collection DOAJ
language English
format Article
sources DOAJ
author Nakamura Shingo
Terashima Masuo
Kikuchi Natsuko
Kimura Minoru
Maehara Tadaaki
Saito Akira
Sato Masahiro
spellingShingle Nakamura Shingo
Terashima Masuo
Kikuchi Natsuko
Kimura Minoru
Maehara Tadaaki
Saito Akira
Sato Masahiro
A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
BMC Nephrology
diphtheria toxin
intravenous injection
plasmid/liposome complex
renal disease
cell ablation
glomerulonephritis
author_facet Nakamura Shingo
Terashima Masuo
Kikuchi Natsuko
Kimura Minoru
Maehara Tadaaki
Saito Akira
Sato Masahiro
author_sort Nakamura Shingo
title A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
title_short A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
title_full A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
title_fullStr A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
title_full_unstemmed A new mouse model for renal lesions produced by intravenous injection of diphtheria toxin A-chain expression plasmid
title_sort new mouse model for renal lesions produced by intravenous injection of diphtheria toxin a-chain expression plasmid
publisher BMC
series BMC Nephrology
issn 1471-2369
publishDate 2004-04-01
description <p>Abstract</p> <p>Background</p> <p>Various animal models of renal failure have been produced and used to investigate mechanisms underlying renal disease and develop therapeutic drugs. Most methods available to produce such models appear to involve subtotal nephrectomy or intravenous administration of antibodies raised against basement membrane of glomeruli. In this study, we developed a novel method to produce mouse models of renal failure by intravenous injection of a plasmid carrying a toxic gene such as diphtheria toxin A-chain (DT-A) gene. DT-A is known to kill cells by inhibiting protein synthesis.</p> <p>Methods</p> <p>An expression plasmid carrying the cytomegalovirus enhancer/chicken β-actin promoter linked to a DT-A gene was mixed with lipid (FuGENE™6) and the resulting complexes were intravenously injected into adult male B6C3F1 mice every day for up to 6 days. After final injection, the kidneys of these mice were sampled on day 4 and weeks 3 and 5.</p> <p>Results</p> <p>H-E staining of the kidney specimens sampled on day 4 revealed remarkable alterations in glomerular compartments, as exemplified by mesangial cell proliferation and formation of extensive deposits in glomerular basement membrane. At weeks 3 and 5, gradual recovery of these tissues was observed. These mice exhibited proteinuria and disease resembling sub-acute glomerulonephritis.</p> <p>Conclusions</p> <p>Repeated intravenous injections of DT-A expression plasmid DNA/lipid complex caused temporary abnormalities mainly in glomeruli of mouse kidney. The disease in these mice resembles sub-acute glomerulonephritis. These DT-A gene-incorporated mice will be useful as animal models in the fields of nephrology and regenerative medicine.</p>
topic diphtheria toxin
intravenous injection
plasmid/liposome complex
renal disease
cell ablation
glomerulonephritis
url http://www.biomedcentral.com/1471-2369/5/4
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