Alexandra Salvi
André Maues De Paula1,2
Nicolas Lévy
Marc Bartoli- 1Aix Marseille Univ, INSERM, Marseille Medical Genetics, Marseille, France
- 2Department of Anatomopathology, CHU La Timone, Marseille, France
- 3Department of Medical Genetics, La Timone Children's Hospital, Marseille, France
- 4Reference Center for Neuromuscular Disease and ALS, Marseille, France
A Commentary on
Long-Term Exercise Reduces Formation of Tubular Aggregates and Promotes Maintenance of Ca2+ Entry Units in Aged Muscle
by Boncompagni, S., Pecorai, C., Michelucci, A., Pietrangelo, L., and Protasi, F. (2021). Front. Physiol. 11:601057. doi: 10.3389/fphys.2020.601057
Introduction
We have read with great interest the study of Boncompagni et al. (2021) on the impact of long-term exercise in aged mice on tubular aggregates (TAs) formation and Ca2+ entry units (CEUs) maintenance. The authors showed a protective effect of long-term voluntary exercise on TA formation in a mouse model developing TAs in the course of aging. As stated by the authors, TAs presence in aged Human skeletal muscles has not been confirmed while it is a constant feature in tubular aggregate myopathy (TAM; MIM #160565 and #610277). TAM is a genetic disease characterized by progressive muscular weakness associated with specific histological features known as TAs. Mutations in STIM1 and ORAI1 encoding genes, the two regulators of store-operated calcium entry (SOCE) have been associated with TAM. The authors previously identified colocalization of these two proteins in CEUs, specific intracellular junctions between sarcoplasmic reticulum (SR) and T-tubules (Boncompagni et al., 2017). In their study, the authors showed an accumulation of these two proteins in aged mice muscles TAs.
We would like to comment on an interesting point in line with our previous study on TAM caused by STIM1 mutations and, in particular, with the asymptomatic family described in our articles (De Paula et al., 2012; Böhm et al., 2013). Indeed, we are convinced that the present work in mice, associated with previous findings in TAM, will bring new insights in muscle diseases associated with tubular aggregates.
Tubular Aggregates Myopathy: Asymptomatic and Symptomatic Families
In the first study on STIM1 mutations associated with TAM (Böhm et al., 2013), we reported one asymptomatic family (Family 4). The proband, aged 30, presented with an elevated CK levels (27x normal levels) detected in a routine medical examination, while his younger brother, aged 24, and his father, aged 59, also presented elevated CK levels (5x and 9x normal levels respectively). None of them developed any muscular symptoms at the time of examination, although an electromyography analysis revealed a slight myopathic pattern for the proband. Further clinical exploration was proposed, and muscles biopsies revealed tubular aggregates, fiber size variation, type I fiber predominance, and type II fiber atrophy. Despite these histological alterations, no muscle weaknesses nor pain was evoked, even for the 59 years old father. Molecular genetics investigations revealed one missense mutation in STIM1 c216C>G [p.(H72Q] in all three patients, affecting the canonical EF-hand in the luminal domain of STIM1 protein. At the time of the publication, we proposed two explanations for the absence of symptoms. First, the specific mutation [p.(H72Q)] by itself being correlated with a particularly mild clinical form; second, the patients' military duties with strong and regular physical training, could be considered as protective from muscle wasting.
Since then, three other families with mutation leading to the same amino acid modification c.216C>A [p.(H72Q)] have been identified (Morin et al., 2019). All the reported patients present muscle weakness occurring during childhood for one patient and during adulthood for the others. Histological analysis revealed classical TAM features together with TAs, fiber size variability and type I fiber predominance observed in muscle biopsies. Some patients also present fibers with centrally localized nuclei and/or vacuoles. These findings indicate that this amino acid mutation has a convincing causative effect on SOCE dysregulation leading to muscular weakness.
Ca2+ Dysregulation and Remodeling of the SR
In vitro studies showed that mutation in STIM1 EF-hand lead to a constitutive activation, an abnormally excessive SOCE influx (Böhm et al., 2013, 2014) and probably to a cytosolic Ca2+ overload in cells. Tubular aggregates originate from the SR and previous studies suggest that their formation involved an altered proteostasis with aggregation of misfolded membrane protein leading to its remodeling (Schiaffino, 2012). The SR is the main Ca2+ stores in skeletal muscle.
Tubular aggregates originates from whole SR and with presence of different SR proteins in mice (Chevessier et al., 2004) and in human (Chevessier et al., 2005). Among these proteins, calsequestrin and SERCA are particularly increased in TAs (Boncompagni et al., 2012). On the one hand, the increase in SERCA protein suggest an increase in Ca2+ entry in SR. On the other hand, calsequestrin increase will decrease free Ca2+ concentration, despite an elevated Ca2+ entry.
In this study, the authors showed, an accumulation of STIM1 and ORAI1 proteins in TAs of aged muscle mice. These two proteins are responsible for SOCE influx.
Together the increased calsequestrin and SERCA proteins with the remodeling of the SR, in particular the formation of TAs through the elongation and increase of internal volume, would allow virtual control of Ca2+ overload.
Discussion
While the precise and complete mechanism remains to be elucidated, according to these findings we suggest that tubular aggregates originate from an altered Ca2+ handling and that their presence is an attempt from the muscle fibers to control Ca2+ overload. Multiple events are associated with TAs development with SR enlargement, an increased in calsequestrin and SERCA and a trapping of SOCE proteins. Eventually, these mechanisms may be synergic or sequential to avoid Ca2+ overload with reducing SOCE proteins availability and a decrease in free Ca2+ concentration within the SR.
As Boncompagni and colleagues have shown in this study, long-term exercise decreases the number of TAs observed on muscle fibers from trained old mice, with a restoration of fatigue resistance and extracellular Ca2+ dependance through preservation of CEUs. Recently, Fodor and colleagues also indicated an improved Ca2+ homeostasis and force with training in aged mouse skeletal muscles (Fodor et al., 2020). We suggest that regular training prevents from Ca2+ dysregulation with a reduced cytosolic or SR Ca2+ overload, even with an enhanced SOCE influx. Indeed, Ca2+ dysregulation and TAs formation in skeletal muscles are found in asymptomatic (no muscular weakness) patients presenting with TAM.
We finally propose that physical activity may explain the absence of muscular weaknesses in this asymptomatic family with a maintained Ca2+ homeostasis. Thus, physical training may be considered as a therapeutic strategy to prevent the disease progression in TAM affected patients.
Author Contributions
AS wrote and edited the manuscript. AM, NL, and SA were responsible for clinical investigations of the patients. MB conceived, directed the study and wrote the manuscript. All authors contributed to the article and approved the submitted version.
Funding
AS received a fellowship from Fondation pour la recherche médicale project number ECO2017 0637467 and from MarMaRa institute number AMX-19-IET-007.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We would to thank J. Laporte for his insightful comments.
References
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Keywords: tubular aggregate myopathy, STIM 1, store operated Ca entry 2+, long-term exercise, genetics disease
Citation: Salvi A, Maues De Paula A, Lévy N, Attarian S and Bartoli M (2021) Commentary: Long-Term Exercise Reduces Formation of Tubular Aggregates and Promotes Maintenance of Ca2+ Entry Units in Aged Muscle. Front. Physiol. 12:663677. doi: 10.3389/fphys.2021.663677
Received: 03 February 2021; Accepted: 09 March 2021;
Published: 01 April 2021.
Edited by:
Elizabeth Vafiadaki, Biomedical Research Foundation of the Academy of Athens (BRFAA), GreeceReviewed by:
D. George Stephenson, La Trobe University, AustraliaCopyright © 2021 Salvi, Maues De Paula, Lévy, Attarian and Bartoli. 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) and the copyright owner(s) 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.
*Correspondence: Marc Bartoli, marc.bartoli@univ-amu.fr