Mitochondria-Ros Crosstalk in the Control of Cell Death and Aging

Author:

Marchi Saverio1,Giorgi Carlotta1,Suski Jan M.12,Agnoletto Chiara1,Bononi Angela1,Bonora Massimo1,De Marchi Elena1,Missiroli Sonia1,Patergnani Simone1,Poletti Federica1,Rimessi Alessandro1,Duszynski Jerzy2,Wieckowski Mariusz R.2,Pinton Paolo1

Affiliation:

1. Department of Experimental and Diagnostic Medicine, Section of General Pathology, Interdisciplinary Center for the Study of Inflammation (ICSI), Laboratory for Technologies of Advanced Therapies (LTTA), University of Ferrara, 44121 Ferrara, Italy

2. Department of Biochemistry, Nencki Institute of Experimental Biology, 02-093 Warsaw, Poland

Abstract

Reactive oxygen species (ROS) are highly reactive molecules, mainly generated inside mitochondria that can oxidize DNA, proteins, and lipids. At physiological levels, ROS function as “redox messengers” in intracellular signalling and regulation, whereas excess ROS induce cell death by promoting the intrinsic apoptotic pathway. Recent work has pointed to a further role of ROS in activation of autophagy and their importance in the regulation of aging. This review will focus on mitochondria as producers and targets of ROS and will summarize different proteins that modulate the redox state of the cell. Moreover, the involvement of ROS and mitochondria in different molecular pathways controlling lifespan will be reported, pointing out the role of ROS as a “balance of power,” directing the cell towards life or death.

Publisher

Hindawi Limited

Subject

Cell Biology,Cellular and Molecular Neuroscience,Biochemistry

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