2013
DOI: 10.1186/1477-5956-11-29
|View full text |Cite
|
Sign up to set email alerts
|

Proteomic analyses of age related changes in A.BY/SnJ mouse hearts

Abstract: BackgroundA.BY/SnJ mice are used to study pathological alterations in the heart due to enteroviral infections. Since age is a well-known factor influencing the susceptibility of mice to infection, response to stress and manifestation of cardiovascular diseases, the myocardial proteome of A.BY/SnJ mice aged 1 and 4 months was comparatively studied using two dimensional-differential in-gel electrophoresis (2D-DIGE) and liquid chromatography tandem mass spectrometry (LC-MS/MS).ResultsComplementary analyses by 2D-… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
7
0

Year Published

2014
2014
2020
2020

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 9 publications
(8 citation statements)
references
References 36 publications
1
7
0
Order By: Relevance
“…This protein is a regulator of transport processes such as vesicular trafficking, docking off transport vesicles with their corresponding acceptor membranes [ 108 ] which is important at early stages of development. The higher expression of this protein at later stages, in this case at P637, could be inferred as an effect leading to endoplasmic reticulum-associated protein degradation by either the proteasome or macroautophagy pathway at higher age [ 109 ]. However, this expression pattern could not be shown for Rho GDP-dissociation inhibitor 1 (Arhgdia) and annexin A5 (Anxa5)) which show a down-regulation at P637.…”
Section: Discussionmentioning
confidence: 99%
“…This protein is a regulator of transport processes such as vesicular trafficking, docking off transport vesicles with their corresponding acceptor membranes [ 108 ] which is important at early stages of development. The higher expression of this protein at later stages, in this case at P637, could be inferred as an effect leading to endoplasmic reticulum-associated protein degradation by either the proteasome or macroautophagy pathway at higher age [ 109 ]. However, this expression pattern could not be shown for Rho GDP-dissociation inhibitor 1 (Arhgdia) and annexin A5 (Anxa5)) which show a down-regulation at P637.…”
Section: Discussionmentioning
confidence: 99%
“…Isoelectric focusing (IEF) was performed using a Multiphor II apparatus (GE Healthcare). The second dimension separation of proteins was done on 12.5% SDS‐polyacrylamide gels (Nishtala et al, ; Thiele et al, ).…”
Section: Methodsmentioning
confidence: 99%
“…This is observed in humans (de Magalhaes et al 2009 ; Peters et al 2015 ; van den Akker et al 2014 ), rodents (de Magalhaes et al 2009 ; Zahn et al 2006 , 2007 ), flies (Cannon et al 2017 ; Girardot et al 2006 ; Landis et al 2004 ; McCarroll et al 2004 ; Pletcher et al 2002 ; Zahn et al 2006 ) and worms (Ma et al 2016 ; McCarroll et al 2004 ) across a range of tissues from skin (highly proliferative) to brain (largely post-mitotic) (Glass et al 2013 ; Hamatani et al 2004 ; Kumar et al 2013 ; Lu et al 2004 ; Zahn et al 2006 ), and is therefore not obviously related to a change in the requirement for mitochondrial biogenesis for proliferation. Reductions in mRNA level of mitochondrial proteins are often fairly small, but are clearly significant as recent proteomic studies in worms and mammals have discovered matching reductions in the ETC, ATP synthase, the tricarboxylic acid cycle and mitochondrial ribosomal proteins (Gomez-Serrano et al 2017 ; Liang et al 2014 ; Nishtala et al 2013 ; Ori et al 2015 ; Stauch et al 2015 ; Walther et al 2015 ; Xu et al 2016 ).…”
Section: Candidates For Gene Expression Hallmarks Of Cellular Ageingmentioning
confidence: 99%