# Time-of-day effects on muscle mitochondria following short-term ablation of satellite cells

**Authors:** Ryan E. Kahn, Fawzan Dinnunhan, Guadalupe Meza, Richard L. Lieber, Orly Lacham-Kaplan, John A. Hawley, Sudarshan Dayanidhi

PMC · DOI: 10.3389/fphys.2025.1613184 · Frontiers in Physiology · 2025-07-02

## TL;DR

This study shows that muscle mitochondria function differently at different times of the day, and satellite cells may play a role in this.

## Contribution

The study reveals that satellite cells influence mitochondrial function in a time-of-day dependent manner.

## Key findings

- Mitochondrial respiration in muscle varies by time-of-day but is not affected by satellite cell ablation.
- Submaximal fatigue in glycolytic muscle is lower in the morning, linked to Bmal1 and CLOCK gene expression rhythms.
- Satellite cells appear to influence mitochondrial function according to the time of day.

## Abstract

Endurance exercise capacity fluctuates by time-of-day due, in part, to molecular clock effects on muscle physiology. As endurance-based exercise relies predominantly on mitochondria for the conversion of cellular energy, fluctuations observed in endurance capacity have been attributed to diurnal variation in mitochondrial respiration and molecular clock KO animals exhibiting blunted mitochondrial function/content. Recently, a circadian profiling of satellite cells (SCs) demonstrated molecular clock, metabolic, and mitochondrial genes exhibit robust oscillation over 24 h while long-term SC ablation impairs endurance exercise capacity. These lines of evidence suggest SC molecular clocks may influence mitochondrial respiration according to time-of-day. We determined whether mitochondrial respiration differs by time-of-day in the presence and absence of SCs in oxidative (soleus, SOL) and glycolytic (tibialis anterior, TA) muscle.

Utilizing a Pax7CRE−ERT2/+; Rosa26DTA/+ mouse model capable of SC ablation (SC+, SC−), we conducted experiments in either the morning, afternoon, or evening.

In both SOL and TA, respiratory coupling ratio (RCR) was lowest and Leak-state respiration (TA) was highest in the morning with no differences observed following SC ablation. Utilizing a submaximal ex vivo fatigue protocol that relies predominantly on mitochondrial energy, we observed that submaximal fatiguability was lower in the morning than afternoon in glycolytic muscle (EDL) (morning-SC
+
: 54 ± 5; afternoon-SC
+
: 36 ± 6 contractions until fatigue, p < 0.05), which corresponded with peak/trough Bmal1 and CLOCK gene expression in muscle.

Collectively, the results from the current study suggest that SCs influence mitochondria in a time-of-day manner.

## Linked entities

- **Genes:** BMAL1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 406], CLOCK (clock circadian regulator) [NCBI Gene 9575]
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Mapk3 (mitogen-activated protein kinase 3) [NCBI Gene 26417] {aka Erk-1, Erk1, Ert2, Esrk1, Mnk1, Mtap2k}, Clock (clock circadian regulator) [NCBI Gene 12753] {aka 5330400M04Rik, KAT13D}, Bmal1 (basic helix-loop-helix ARNT like 1) [NCBI Gene 11865] {aka Arnt3, Arntl, BMAL1b, MOP3, bHLHe5, bmal1b'}, Pax7 (paired box 7) [NCBI Gene 18509] {aka Pax-7}
- **Diseases:** fatigue (MESH:D005221)
- **Species:** Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12263925/full.md

## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12263925/full.md

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Source: https://tomesphere.com/paper/PMC12263925