Literature DB >> 25608554

Peroxisomes in cardiomyocytes and the peroxisome / peroxisome proliferator-activated receptor-loop.

Claudia Colasante, Jiangping Chen, Barbara Ahlemeyer, Eveline Baumgart-Vogt1.   

Abstract

It is well established that the heart is strongly dependent on fatty acid metabolism. In cardiomyocytes there are two distinct sites for the β-oxidisation of fatty acids: the mitochondrion and the peroxisome. Although the metabolism of these two organelles is believed to be tightly coupled, the nature of this relationship has not been fully investigated. Recent research has established the significant contribution of mitochondrial function to cardiac ATP production under normal and pathological conditions. In contrast, limited information is available on peroxisomal function in the heart. This is despite these organelles harbouring metabolic pathways that are potentially cardio-protective, and findings that patients with peroxisomal diseases, such as adult Refsum´s disease, can develop heart failure. In this article, we provide a comprehensive overview on the current knowledge of peroxisomes and the regulation of lipid metabolism by PPARs in cardiomyocytes. We also present new experimental evidence on the differential expression of peroxisome-related genes in the heart chambers and demonstrate that even a mild peroxisomal biogenesis defect (Pex11α-/-) can induce profound alterations in the cardiomyocyte´s peroxisomal compartment and related gene expression, including the concomitant deregulation of specific PPARs. The possible impact of peroxisomal dysfunction in the heart is discussed and a model for the modulation of myocardial metabolism via a peroxisome/PPAR-loop is proposed.

Entities:  

Keywords:  Peroxisome; heart failure; peroxisomal disorders; peroxisome proliferator-activated receptor; β-oxidation of fatty acids

Mesh:

Substances:

Year:  2015        PMID: 25608554     DOI: 10.1160/TH14-06-0497

Source DB:  PubMed          Journal:  Thromb Haemost        ISSN: 0340-6245            Impact factor:   5.249


  23 in total

1.  Pex35 is a regulator of peroxisome abundance.

Authors:  Ido Yofe; Kareem Soliman; Silvia G Chuartzman; Bruce Morgan; Uri Weill; Eden Yifrach; Tobias P Dick; Sara J Cooper; Christer S Ejsing; Maya Schuldiner; Einat Zalckvar; Sven Thoms
Journal:  J Cell Sci       Date:  2017-01-03       Impact factor: 5.285

2.  Compromised peroxisomes in idiopathic pulmonary fibrosis, a vicious cycle inducing a higher fibrotic response via TGF-β signaling.

Authors:  Gani Oruqaj; Srikanth Karnati; Vijith Vijayan; Lakshmi Kanth Kotarkonda; Eistine Boateng; Wenming Zhang; Clemens Ruppert; Andreas Günther; Wei Shi; Eveline Baumgart-Vogt
Journal:  Proc Natl Acad Sci U S A       Date:  2015-04-06       Impact factor: 11.205

3.  Changes in the activity of some metabolic enzymes in the heart of SHR rat incurred by transgenic expression of CD36.

Authors:  Dmitry Manakov; David Kolar; Jitka Zurmanova; Michal Pravenec; Jiri Novotny
Journal:  J Physiol Biochem       Date:  2018-06-18       Impact factor: 4.158

4.  New insights into the distribution, protein abundance and subcellular localisation of the endogenous peroxisomal biogenesis proteins PEX3 and PEX19 in different organs and cell types of the adult mouse.

Authors:  Claudia Colasante; Jiangping Chen; Barbara Ahlemeyer; Rocio Bonilla-Martinez; Srikanth Karnati; Eveline Baumgart-Vogt
Journal:  PLoS One       Date:  2017-08-17       Impact factor: 3.240

5.  Mechanistic insights into the augmented effect of bone marrow mesenchymal stem cells and thiazolidinediones in streptozotocin-nicotinamide induced diabetic rats.

Authors:  Alaaeldin Ahmed Hamza; Ebtehal Mohammad Fikry; Wedad Abdallah; Amr Amin
Journal:  Sci Rep       Date:  2018-06-29       Impact factor: 4.379

6.  Peroxisomes in host defense.

Authors:  Francesca Di Cara
Journal:  PLoS Pathog       Date:  2020-07-02       Impact factor: 6.823

7.  Peroxisomes in Different Skeletal Cell Types during Intramembranous and Endochondral Ossification and Their Regulation during Osteoblast Differentiation by Distinct Peroxisome Proliferator-Activated Receptors.

Authors:  Guofeng Qian; Wei Fan; Barbara Ahlemeyer; Srikanth Karnati; Eveline Baumgart-Vogt
Journal:  PLoS One       Date:  2015-12-02       Impact factor: 3.240

8.  Downregulation of GSTK1 Is a Common Mechanism Underlying Hypertrophic Cardiomyopathy.

Authors:  Shota Sasagawa; Yuhei Nishimura; Shiko Okabe; Soichiro Murakami; Yoshifumi Ashikawa; Mizuki Yuge; Koki Kawaguchi; Reiko Kawase; Ryuji Okamoto; Masaaki Ito; Toshio Tanaka
Journal:  Front Pharmacol       Date:  2016-06-14       Impact factor: 5.810

9.  ESCRT-III is required for scissioning new peroxisomes from the endoplasmic reticulum.

Authors:  Fred D Mast; Thurston Herricks; Kathleen M Strehler; Leslie R Miller; Ramsey A Saleem; Richard A Rachubinski; John D Aitchison
Journal:  J Cell Biol       Date:  2018-03-27       Impact factor: 10.539

10.  Dysfunctional peroxisomes compromise gut structure and host defense by increased cell death and Tor-dependent autophagy.

Authors:  Francesca Di Cara; Margret H Bülow; Andrew J Simmonds; Richard A Rachubinski
Journal:  Mol Biol Cell       Date:  2018-09-06       Impact factor: 4.138

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