Cargando…

Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases

Research over the last decade strengthened the understanding that skeletal muscles are not only the major tissue in the body from a volume point of view but also function as a master regulator contributing to optimal organismal health. These new contributions to the available body of knowledge trigg...

Descripción completa

Detalles Bibliográficos
Autores principales: Manring, Heather, Abreu, Eduardo, Brotto, Leticia, Weisleder, Noah, Brotto, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927072/
https://www.ncbi.nlm.nih.gov/pubmed/24600395
http://dx.doi.org/10.3389/fphys.2014.00037
_version_ 1782304061019652096
author Manring, Heather
Abreu, Eduardo
Brotto, Leticia
Weisleder, Noah
Brotto, Marco
author_facet Manring, Heather
Abreu, Eduardo
Brotto, Leticia
Weisleder, Noah
Brotto, Marco
author_sort Manring, Heather
collection PubMed
description Research over the last decade strengthened the understanding that skeletal muscles are not only the major tissue in the body from a volume point of view but also function as a master regulator contributing to optimal organismal health. These new contributions to the available body of knowledge triggered great interest in the roles of skeletal muscle beyond contraction. The World Health Organization, through its Global Burden of Disease (GBD) report, recently raised further awareness about the key importance of skeletal muscles as the GDB reported musculoskeletal (MSK) diseases have become the second greatest cause of disability, with more than 1.7 billion people in the globe affected by a diversity of MSK conditions. Besides their role in MSK disorders, skeletal muscles are also seen as principal metabolic organs with essential contributions to metabolic disorders, especially those linked to physical inactivity. In this review, we have focused on the unique function of new genes/proteins (i.e., MTMR14, MG29, sarcalumenin, KLF15) that during the last few years have helped provide novel insights about muscle function in health and disease, muscle fatigue, muscle metabolism, and muscle aging. Next, we provide an in depth discussion of how these genes/proteins converge into a common function of acting as regulators of intracellular calcium homeostasis. A clear link between dysfunctional calcium homeostasis is established and the special role of store-operated calcium entry is analyzed. The new knowledge that has been generated by the understanding of the roles of previously unknown modulatory genes of the skeletal muscle excitation-contraction coupling (ECC) process brings exciting new possibilities for treatment of MSK diseases, muscle regeneration, and skeletal muscle tissue engineering. The next decade of skeletal muscle and MSK research is bound to bring to fruition applied knowledge that will hopefully offset the current heavy and sad burden of MSK diseases on the planet.
format Online
Article
Text
id pubmed-3927072
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-39270722014-03-05 Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases Manring, Heather Abreu, Eduardo Brotto, Leticia Weisleder, Noah Brotto, Marco Front Physiol Physiology Research over the last decade strengthened the understanding that skeletal muscles are not only the major tissue in the body from a volume point of view but also function as a master regulator contributing to optimal organismal health. These new contributions to the available body of knowledge triggered great interest in the roles of skeletal muscle beyond contraction. The World Health Organization, through its Global Burden of Disease (GBD) report, recently raised further awareness about the key importance of skeletal muscles as the GDB reported musculoskeletal (MSK) diseases have become the second greatest cause of disability, with more than 1.7 billion people in the globe affected by a diversity of MSK conditions. Besides their role in MSK disorders, skeletal muscles are also seen as principal metabolic organs with essential contributions to metabolic disorders, especially those linked to physical inactivity. In this review, we have focused on the unique function of new genes/proteins (i.e., MTMR14, MG29, sarcalumenin, KLF15) that during the last few years have helped provide novel insights about muscle function in health and disease, muscle fatigue, muscle metabolism, and muscle aging. Next, we provide an in depth discussion of how these genes/proteins converge into a common function of acting as regulators of intracellular calcium homeostasis. A clear link between dysfunctional calcium homeostasis is established and the special role of store-operated calcium entry is analyzed. The new knowledge that has been generated by the understanding of the roles of previously unknown modulatory genes of the skeletal muscle excitation-contraction coupling (ECC) process brings exciting new possibilities for treatment of MSK diseases, muscle regeneration, and skeletal muscle tissue engineering. The next decade of skeletal muscle and MSK research is bound to bring to fruition applied knowledge that will hopefully offset the current heavy and sad burden of MSK diseases on the planet. Frontiers Media S.A. 2014-02-18 /pmc/articles/PMC3927072/ /pubmed/24600395 http://dx.doi.org/10.3389/fphys.2014.00037 Text en Copyright © 2014 Manring, Abreu, Brotto, Weisleder and Brotto. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Manring, Heather
Abreu, Eduardo
Brotto, Leticia
Weisleder, Noah
Brotto, Marco
Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title_full Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title_fullStr Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title_full_unstemmed Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title_short Novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
title_sort novel excitation-contraction coupling related genes reveal aspects of muscle weakness beyond atrophy—new hopes for treatment of musculoskeletal diseases
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3927072/
https://www.ncbi.nlm.nih.gov/pubmed/24600395
http://dx.doi.org/10.3389/fphys.2014.00037
work_keys_str_mv AT manringheather novelexcitationcontractioncouplingrelatedgenesrevealaspectsofmuscleweaknessbeyondatrophynewhopesfortreatmentofmusculoskeletaldiseases
AT abreueduardo novelexcitationcontractioncouplingrelatedgenesrevealaspectsofmuscleweaknessbeyondatrophynewhopesfortreatmentofmusculoskeletaldiseases
AT brottoleticia novelexcitationcontractioncouplingrelatedgenesrevealaspectsofmuscleweaknessbeyondatrophynewhopesfortreatmentofmusculoskeletaldiseases
AT weisledernoah novelexcitationcontractioncouplingrelatedgenesrevealaspectsofmuscleweaknessbeyondatrophynewhopesfortreatmentofmusculoskeletaldiseases
AT brottomarco novelexcitationcontractioncouplingrelatedgenesrevealaspectsofmuscleweaknessbeyondatrophynewhopesfortreatmentofmusculoskeletaldiseases