Oncotarget

Research Papers: Gerotarget (Focus on Aging):

A mutation in the NADH-dehydrogenase subunit 2 suppresses fibroblast aging

Marianne Schauer _, Tina Kottek, Madeleine Schönherr, Animesh Bhattacharya, Saleh M. Ibrahim, Misa Hirose, Rüdiger Köhling, Georg Fuellen, Ulf Schmitz and Manfred Kunz

PDF  |  HTML  |  Supplementary Files  |  How to cite  |  Order a Reprint

Oncotarget. 2015; 6:8552-8566. https://doi.org/10.18632/oncotarget.3298

Metrics: PDF 1456 views  |   HTML 2294 views  |   ?  


Abstract

Marianne Schauer1, Tina Kottek1, Madeleine Schönherr1, Animesh Bhattacharya1, Saleh M Ibrahim2, Misa Hirose2, Rüdiger Köhling3, Georg Fuellen4, Ulf Schmitz5, Manfred Kunz1

1Department of Dermatology, Venereology and Allergology, University of Leipzig, Leipzig 04103, Germany

2Department of Dermatology, Allergology and Venereology, University of Lübeck, Lübeck 23538, Germany

3Department of Physiology, University of Rostock, Rostock 18057, Germany

4Department of Biostatistics and Informatics in Medicine and Ageing Research, University of Rostock, Rostock 18057, Germany

5Department of Systems Biology and Bioinformatics, University of Rostock, Rostock 18057, Germany

Correspondence to:

Marianne Schauer, e-mail: Marianne.Schauer@medizin.uni-leipzig.de

Keywords: aging, senescence, mitochondria, skin fibroblasts, p38MAPK signalling

Received: January 23, 2015     Accepted: February 08, 2015     Published: March 24, 2015

ABSTRACT

Mutations of mitochondrial (mt)DNA cause a variety of human diseases and are implicated in premature aging syndromes. Here we investigated a single nucleotide exchange (leucine to methionine) at position nt4738 in the mitochondrial NADH dehydrogenase subunit 2 (Nd2) gene of the respiratory chain. Primary fibroblasts derived from the conplastic mouse strain C57BL/6J-mtALR/LTJ with mutant enzyme, possessed high enzyme activity and ATP production and low ROS production. Furthermore, Nd2-mutant fibroblasts expressed lower senescence markers. Transcriptome analysis revealed that the members of the p38MAPK pathway were significantly downregulated in Nd2-mutant mice. In agreement, inhibition of p38MAPK with SB203580 enhanced proliferation and reduced cytokine secretion in fibroblasts. In Nd2-mutant mouse skin, the amount of Ki67-positive cells was significantly higher than in control skin. The higher amount of Ki67-positive cells and the thicker epidermis in Nd2-mutant mice strongly supported the in vitro data. In conclusion, Nd2 is a mitochondrial gene, involved in age-related signaling pathways.


Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 3.0 License.
PII: 3298