Suppr超能文献

C57BL/6 近交系遗传工程小鼠与其野生型对照品系的错配会导致混杂结果,这在对乙酰氨基酚和刀豆蛋白 A 肝损伤中 JNK2 的研究中就是如此。

Mispairing C57BL/6 substrains of genetically engineered mice and wild-type controls can lead to confounding results as it did in studies of JNK2 in acetaminophen and concanavalin A liver injury.

机构信息

Molecular and Cellular Toxicology Section, Laboratory of Molecular Immunology, National Heart, Lung, and Blood Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892-1760, United States.

出版信息

Chem Res Toxicol. 2011 Jun 20;24(6):794-6. doi: 10.1021/tx200143x. Epub 2011 May 24.

Abstract

C57BL/6 mice are widely used in biomedical research for the background of genetically engineered mice (GEM) and wild-type controls with the belief that the genetic background of GEM and control mice differ significantly by only one or more altered genes. This principle, however, does have limitations due in part to the existence of multiple substrains of C57BL/6 mice that should not be used interchangeably as they can differ both genetically and phenotypically. We show here that these mispairings do occur frequently and can lead to inaccurate and conflicting findings.

摘要

C57BL/6 小鼠广泛应用于生物医学研究,其背景是基因工程小鼠(GEM)和野生型对照小鼠,人们认为 GEM 和对照小鼠的遗传背景仅因一个或多个改变的基因而有显著差异。然而,这一原则确实存在局限性,部分原因是 C57BL/6 小鼠存在多个亚系,这些亚系不应互换使用,因为它们在遗传和表型上都可能存在差异。我们在这里表明,这些错配经常发生,并可能导致不准确和相互矛盾的发现。

相似文献

2
Combined Activities of JNK1 and JNK2 in Hepatocytes Protect Against Toxic Liver Injury.
Gastroenterology. 2016 Apr;150(4):968-81. doi: 10.1053/j.gastro.2015.12.019. Epub 2015 Dec 19.
3
Protective role of c-Jun N-terminal kinase 2 in acetaminophen-induced liver injury.
Biochem Biophys Res Commun. 2008 Sep 12;374(1):6-10. doi: 10.1016/j.bbrc.2008.06.065. Epub 2008 Jun 27.
4
c-Jun N-terminal kinase plays a major role in murine acetaminophen hepatotoxicity.
Gastroenterology. 2006 Jul;131(1):165-78. doi: 10.1053/j.gastro.2006.03.045.
5
What is your diagnosis? Serum biochemical data from genetically modified mice.
Vet Clin Pathol. 2012 Jun;41(2):301-2. doi: 10.1111/j.1939-165X.2012.00428.x. Epub 2012 May 2.
7
Mitogen-activated protein kinase phosphatase (Mkp)-1 protects mice against acetaminophen-induced hepatic injury.
Toxicol Pathol. 2012 Dec;40(8):1095-105. doi: 10.1177/0192623312447551. Epub 2012 May 23.
8
Acetaminophen-induced liver injury is attenuated in transgenic fat-1 mice endogenously synthesizing long-chain n-3 fatty acids.
Biochem Pharmacol. 2018 Aug;154:75-88. doi: 10.1016/j.bcp.2018.04.019. Epub 2018 Apr 18.
9
Protective role of c-Jun N-terminal kinase-2 (JNK2) in ibuprofen-induced acute liver injury.
J Pathol. 2019 Jan;247(1):110-122. doi: 10.1002/path.5174. Epub 2018 Dec 11.
10
Endogenous interleukin-4 regulates glutathione synthesis following acetaminophen-induced liver injury in mice.
Chem Res Toxicol. 2012 Jan 13;25(1):83-93. doi: 10.1021/tx2003992. Epub 2011 Dec 13.

引用本文的文献

1
Inducible nitric oxide synthase (iNOS): More than an inducible enzyme? Rethinking the classification of NOS isoforms.
Pharmacol Res. 2025 Jun;216:107781. doi: 10.1016/j.phrs.2025.107781. Epub 2025 May 17.
2
The multiple mechanisms and modes of cell death after acetaminophen overdose.
Explor Dig Dis. 2025;4. doi: 10.37349/edd.2025.100569. Epub 2025 Apr 7.
3
Whole exome sequencing as a screening tool in dogs: A pilot study.
Comput Struct Biotechnol J. 2025 Mar 7;27:960-968. doi: 10.1016/j.csbj.2025.03.008. eCollection 2025.
8
Phenylpropionic acid produced by gut microbiota alleviates acetaminophen-induced hepatotoxicity.
Gut Microbes. 2023 Jan-Dec;15(1):2231590. doi: 10.1080/19490976.2023.2231590.
9
Genetic quality: a complex issue for experimental study reproducibility.
Transgenic Res. 2022 Oct;31(4-5):413-430. doi: 10.1007/s11248-022-00314-w. Epub 2022 Jun 25.

本文引用的文献

1
Genetic polymorphisms among C57BL/6 mouse inbred strains.
Transgenic Res. 2011 Jun;20(3):481-9. doi: 10.1007/s11248-010-9403-8. Epub 2010 May 27.
2
Diet-induced obesity in two C57BL/6 substrains with intact or mutant nicotinamide nucleotide transhydrogenase (Nnt) gene.
Obesity (Silver Spring). 2010 Oct;18(10):1902-5. doi: 10.1038/oby.2009.477. Epub 2010 Jan 7.
3
Differences in aggressive behavior and DNA copy number variants between BALB/cJ and BALB/cByJ substrains.
Behav Genet. 2010 Mar;40(2):201-10. doi: 10.1007/s10519-009-9325-5. Epub 2009 Dec 23.
4
Effects of oats on plasma cholesterol and lipoproteins in C57BL/6 mice are substrain specific.
Br J Nutr. 2010 Feb;103(4):513-21. doi: 10.1017/S000711450999211X. Epub 2009 Oct 20.
5
Genetic differences among C57BL/6 substrains.
Exp Anim. 2009 Apr;58(2):141-9. doi: 10.1538/expanim.58.141.
7
Differential roles of JNK in ConA/GalN and ConA-induced liver injury in mice.
Am J Pathol. 2008 Oct;173(4):962-72. doi: 10.2353/ajpath.2008.080358. Epub 2008 Sep 4.
9
Protective role of c-Jun N-terminal kinase 2 in acetaminophen-induced liver injury.
Biochem Biophys Res Commun. 2008 Sep 12;374(1):6-10. doi: 10.1016/j.bbrc.2008.06.065. Epub 2008 Jun 27.
10
Alcohol trait and transcriptional genomic analysis of C57BL/6 substrains.
Genes Brain Behav. 2008 Aug;7(6):677-89. doi: 10.1111/j.1601-183X.2008.00405.x. Epub 2008 Apr 7.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验