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Correction to Cells 2025, 14(19), 1517.
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Correction

Correction: Singlár et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517

1
Department of Physiology, Faculty of Medicine, University of Debrecen, 4032 Debrecen, Hungary
2
HUN-REN Cell Physiology Research Group, University of Debrecen, 4032 Debrecen, Hungary
3
Doctoral School of Molecular Medicine, University of Debrecen, 4032 Debrecen, Hungary
4
Department of Biochemistry, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary
5
Centre of Excellence for Interdisciplinary Research, Development and Innovation, University of Szeged, 6720 Szeged, Hungary
6
Institute of Surgical Research, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary
7
Medical GeneTechnology Unit, HUN-REN Institute of Experimental Medicine, 1083 Budapest, Hungary
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Cells 2026, 15(9), 742; https://doi.org/10.3390/cells15090742
Submission received: 18 March 2026 / Accepted: 25 March 2026 / Published: 22 April 2026
Missing Citation
In the original publication [1], Ref. [2] was not cited. The citation has now been inserted in the Discussion, 2nd paragraph, and should read:
We replicated the genetic engineering strategy described by Hebert-Chatelain in 2016 [39], which is aimed at interfering with mitochondrial targeting by specifically disrupting only the mitochondrial pool of CB1Rs while leaving plasma membrane CB1Rs intact (Figure 1A). The strategy involves removing 63 nucleotides (21 amino acids) that have been identified as being responsible for the mitochondrial targeting of the receptor. The exact mutation was published in an elegant study by Soria-Gomez et al. in 2021 [58].
Text Correction
There was an error in the original publication. We incorrectly claimed that we investigated the first-ever global mitochondrial CB1 knockout mouse model.
A correction has been made to the last paragraph of the Introduction:
In the current study we created a global mitochondrial CB1 receptor mouse model. By using a combination of genetic and pharmacological approaches, we report a key role of mtCB1Rs in skeletal muscle physiology. Our findings offer novel insights into the complex involvement of mtCB1Rs in ECS-mediated regulation of skeletal muscle contraction, force generation, mitochondrial morphology, and energetics.
A correction has been made to the first paragraph of the Discussion:
In this work, employing a systemic mitochondrial CB1 deletion murine model, we explored the multifaceted consequences of the suppression of mtCB1 expression, primarily impacting muscle force, muscle mitochondrial morphology, respiration, membrane potential, as well as calcium levels.
A correction has been made to the first paragraph of the Conclusion:
Our findings obtained on the newly generated systemic mtCB1-KO mouse model align with the hypothesis that mitochondrial CB1 receptors play a critical role in maintaining mitochondrial health and function, which in turn impacts overall muscle performance. Suppression of mtCB1 expression leads to mitochondrial dysfunction at a very fundamental level, directly impacting energy production and, consequently, skeletal muscle performance.
References
Added Reference 58: Soria-Gomez, E.; Pagano Zottola, A.C.; Mariani, Y.; Desprez, T.; Barresi, M.; Río, I.B.-D.; Muguruza, C.; Bon-Jego, M.L.; Julio-Kalajzić, F.; Flynn, R. Subcellular specificity of cannabinoid effects in striatonigral circuits. Neuron 2021, 9, 1513–1526.e11. https://doi.org/10.1016/j.neuron.2021.03.007. With this correction, the order of some references has been adjusted accordingly.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

References

  1. Singlár, Z.; Szentesi, P.; Ganbat, N.; Horváth, B.; Juhász, L.; Gönczi, M.; Keller-Pintér, A.; Oláh, A.; Máté, Z.; Erdélyi, F.; et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517. [Google Scholar] [CrossRef] [PubMed]
  2. Soria-Gomez, E.; Pagano Zottola, A.C.; Mariani, Y.; Desprez, T.; Barresi, M.; Río, I.B.-D.; Muguruza, C.; Bon-Jego, M.L.; Julio-Kalajzić, F.; Flynn, R. Subcellular specificity of cannabinoid effects in striatonigral circuits. Neuron 2021, 9, 1513–1526.e11. [Google Scholar] [CrossRef] [PubMed]
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MDPI and ACS Style

Singlár, Z.; Szentesi, P.; Ganbat, N.; Horváth, B.; Juhász, L.; Gönczi, M.; Keller-Pintér, A.; Oláh, A.; Máté, Z.; Erdélyi, F.; et al. Correction: Singlár et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517. Cells 2026, 15, 742. https://doi.org/10.3390/cells15090742

AMA Style

Singlár Z, Szentesi P, Ganbat N, Horváth B, Juhász L, Gönczi M, Keller-Pintér A, Oláh A, Máté Z, Erdélyi F, et al. Correction: Singlár et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517. Cells. 2026; 15(9):742. https://doi.org/10.3390/cells15090742

Chicago/Turabian Style

Singlár, Zoltán, Péter Szentesi, Nyamkhuu Ganbat, Barnabás Horváth, László Juhász, Mónika Gönczi, Anikó Keller-Pintér, Attila Oláh, Zoltán Máté, Ferenc Erdélyi, and et al. 2026. "Correction: Singlár et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517" Cells 15, no. 9: 742. https://doi.org/10.3390/cells15090742

APA Style

Singlár, Z., Szentesi, P., Ganbat, N., Horváth, B., Juhász, L., Gönczi, M., Keller-Pintér, A., Oláh, A., Máté, Z., Erdélyi, F., Csernoch, L., & Sztretye, M. (2026). Correction: Singlár et al. Revealing the Specific Contributions of Mitochondrial CB1 Receptors to the Overall Function of Skeletal Muscle in Mice. Cells 2025, 14, 1517. Cells, 15(9), 742. https://doi.org/10.3390/cells15090742

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