16
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Mitochondrial stress and mitokines in aging

      review-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Mitokines are signaling molecules that enable communication of local mitochondrial stress to other mitochondria in distant cells and tissues. Among those molecules are FGF21, GDF15 (both expressed in the nucleus) and several mitochondrial‐derived peptides, including humanin. Their responsiveness to mitochondrial stress induces mitokine‐signaling in response for example to exercise, following mitochondrial challenges in skeletal muscle. Such signaling is emerging as an important mediator of exercise‐derived and dietary strategy‐related molecular and systemic health benefits, including healthy aging. A compensatory increase in mitokine synthesis and secretion could preserve mitochondrial function and overall cellular vitality. Conversely, resistance against mitokine actions may also develop. Alterations of mitokine‐levels, and therefore of mitokine‐related inter‐tissue cross talk, are associated with general aging processes and could influence the development of age‐related chronic metabolic, cardiovascular and neurological diseases; whether these changes contribute to aging or represent “rescue factors” remains to be conclusively shown. The aim of the present review is to summarize the expanding knowledge on mitokines, the potential to modulate them by lifestyle and their involvement in aging and age‐related diseases. We highlight the importance of well‐balanced mitokine‐levels, the preventive and therapeutic properties of maintaining mitokine homeostasis and sensitivity of mitokine signaling but also the risks arising from the dysregulation of mitokines. While reduced mitokine levels may impair inter‐organ crosstalk, also excessive mitokine concentrations can have deleterious consequences and are associated with conditions such as cancer and heart failure. Preservation of healthy mitokine signaling levels can be achieved by regular exercise and is associated with an increased lifespan.

          Abstract

          Mitokines signal mitochondrial stress to distant cells and tissues. Long‐lasting increases or decreases in mitokine levels are associated with diseases and age‐related functional decline. Controlled fluctuations of mitokines, such as in exercise, may improve mitokine sensitivity and promote healthy aging.

          Related collections

          Most cited references168

          • Record: found
          • Abstract: found
          • Article: not found

          Chronic inflammation (inflammaging) and its potential contribution to age-associated diseases.

          Human aging is characterized by a chronic, low-grade inflammation, and this phenomenon has been termed as "inflammaging." Inflammaging is a highly significant risk factor for both morbidity and mortality in the elderly people, as most if not all age-related diseases share an inflammatory pathogenesis. Nevertheless, the precise etiology of inflammaging and its potential causal role in contributing to adverse health outcomes remain largely unknown. The identification of pathways that control age-related inflammation across multiple systems is therefore important in order to understand whether treatments that modulate inflammaging may be beneficial in old people. The session on inflammation of the Advances in Gerosciences meeting held at the National Institutes of Health/National Institute on Aging in Bethesda on October 30 and 31, 2013 was aimed at defining these important unanswered questions about inflammaging. This article reports the main outcomes of this session. © The Author 2014. Published by Oxford University Press on behalf of The Gerontological Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Integrative biology of exercise.

            Exercise represents a major challenge to whole-body homeostasis provoking widespread perturbations in numerous cells, tissues, and organs that are caused by or are a response to the increased metabolic activity of contracting skeletal muscles. To meet this challenge, multiple integrated and often redundant responses operate to blunt the homeostatic threats generated by exercise-induced increases in muscle energy and oxygen demand. The application of molecular techniques to exercise biology has provided greater understanding of the multiplicity and complexity of cellular networks involved in exercise responses, and recent discoveries offer perspectives on the mechanisms by which muscle "communicates" with other organs and mediates the beneficial effects of exercise on health and performance.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Mitochondria and cancer.

              Contrary to conventional wisdom, functional mitochondria are essential for the cancer cell. Although mutations in mitochondrial genes are common in cancer cells, they do not inactivate mitochondrial energy metabolism but rather alter the mitochondrial bioenergetic and biosynthetic state. These states communicate with the nucleus through mitochondrial 'retrograde signalling' to modulate signal transduction pathways, transcriptional circuits and chromatin structure to meet the perceived mitochondrial and nuclear requirements of the cancer cell. Cancer cells then reprogramme adjacent stromal cells to optimize the cancer cell environment. These alterations activate out-of-context programmes that are important in development, stress response, wound healing and nutritional status.
                Bookmark

                Author and article information

                Contributors
                johannes.burtscher@unil.ch
                k.khoramipour@gmail.com
                akhamoui@fau.edu
                Journal
                Aging Cell
                Aging Cell
                10.1111/(ISSN)1474-9726
                ACEL
                Aging Cell
                John Wiley and Sons Inc. (Hoboken )
                1474-9718
                1474-9726
                15 January 2023
                February 2023
                : 22
                : 2 ( doiID: 10.1111/acel.v22.2 )
                : e13770
                Affiliations
                [ 1 ] Institute of Sport Sciences University of Lausanne Lausanne Switzerland
                [ 2 ] Department of Biomedical Sciences University of Lausanne Lausanne Switzerland
                [ 3 ] Department of Biology, Faculty of Science University of Shiraz Shiraz Iran
                [ 4 ] Department of Exercise Science and Health Promotion Florida Atlantic University Boca Raton Florida USA
                [ 5 ] Department of Sport Science University of Innsbruck Innsbruck Austria
                [ 6 ] Department of Physiology and Pharmacology, Neuroscience Research Center, Institute of Neuropharmacology, and Afzalipour School of Medicine Kerman University of Medical Sciences Kerman Iran
                Author notes
                [*] [* ] Correspondence

                Johannes Burtscher, Institute of Sport Sciences, University of Lausanne, 1015 Lausanne, Switzerland.

                Email: johannes.burtscher@ 123456unil.ch

                Kayvan Khoramipour, Department of Physiology and Pharmacology, Neuroscience Research Center, Institute of Neuropharmacology, Afzalipour School of Medicine, Kerman University of Medical Sciences, Kerman, Iran.

                Email: k.khoramipour@ 123456gmail.com

                Andy V. Khamoui, Department of Exercise Science and Health Promotion, Florida Atlantic University, Boca Raton, FL, USA.

                Email: akhamoui@ 123456fau.edu

                Author information
                https://orcid.org/0000-0002-2889-0151
                https://orcid.org/0000-0002-5232-3632
                https://orcid.org/0000-0003-4449-536X
                Article
                ACEL13770 ACE-22-0741-R.R1
                10.1111/acel.13770
                9924952
                36642986
                e684dba6-4f9a-44b6-b59c-f6b017bdd882
                © 2023 The Authors. Aging Cell published by Anatomical Society and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 08 December 2022
                : 19 October 2022
                : 20 December 2022
                Page count
                Figures: 3, Tables: 0, Pages: 18, Words: 16328
                Categories
                Review Article
                Review Article
                Custom metadata
                2.0
                February 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.5 mode:remove_FC converted:13.02.2023

                Cell biology
                fgf21,gdf15,humanin,mitochondria‐derived peptides,mitochondrial stress response,mitohormesis,mitokines

                Comments

                Comment on this article