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Correction

Correction: Dai et al. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400

Department of Pediatrics, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou 510080, China
*
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Nutrients 2025, 17(22), 3554; https://doi.org/10.3390/nu17223554
Submission received: 2 July 2025 / Accepted: 2 July 2025 / Published: 14 November 2025
In the original publication [1], there was a mistake in Figure 5D. The Western blot image was mistakenly uploaded. The authors formally requested the replacement of the Western blot image presented in Figure 5D. The corrected Figure 5D appears below. The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Dai, J.-M.; Yu, M.-X.; Shen, Z.-Y.; Guo, C.-Y.; Zhuang, S.-Q.; Qiu, X.-S. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400. [Google Scholar] [CrossRef]
Figure 5. Involvement of mTORC1 in leucine-stimulated differentiation of primary satellite cells. (A) Primary preterm rat satellite cells reaching approximately 80% confluence, were induced to differentiate by differentiation medium. Cells lyse every 24 h and the lysates subjected to Western analysis. MyoD and myogenin densitometry values were adjusted to GAPDH intensity, and then normalized to the control group (d0). * p < 0.05, ** p < 0.01 vs. control; (B) Confluent primary satellite cells cultured in differentiation medium with varying concentrations of leucine for 1 h. When indicated by “+”, cells received 50 nM rapamycin. We used western blot assay to detect the expression of mTOR and phospho-mTOR. Phospho-mTOR densitometry values were adjusted to total mTOR intensity, and then normalized to expression from the control group (0 mM leucine); (C) Confluent primary satellite cells were cultured in differentiation medium with different concentrations of leucine for 8 h, followed by western blot analysis. MyoD densitometry values were adjusted to GAPDH intensity and then normalized to expression from the control group (0 mM leucine); (D) Confluent primary satellite cells were cultured in differentiation medium with different concentrations of leucine for 3 days, followed by Western analysis. Myogenin densitometry values were adjusted to GAPDH intensity and then normalized to expression from the control group (0 mM leucine). * p < 0.05, ** p < 0.01, *** p < 0.01 vs. control (0 mM leucine). # p < 0.05, ## p < 0.01 vs. 2.0 mM leucine. All data are shown as the mean ± SD of three independent experiments and representative images are shown.
Figure 5. Involvement of mTORC1 in leucine-stimulated differentiation of primary satellite cells. (A) Primary preterm rat satellite cells reaching approximately 80% confluence, were induced to differentiate by differentiation medium. Cells lyse every 24 h and the lysates subjected to Western analysis. MyoD and myogenin densitometry values were adjusted to GAPDH intensity, and then normalized to the control group (d0). * p < 0.05, ** p < 0.01 vs. control; (B) Confluent primary satellite cells cultured in differentiation medium with varying concentrations of leucine for 1 h. When indicated by “+”, cells received 50 nM rapamycin. We used western blot assay to detect the expression of mTOR and phospho-mTOR. Phospho-mTOR densitometry values were adjusted to total mTOR intensity, and then normalized to expression from the control group (0 mM leucine); (C) Confluent primary satellite cells were cultured in differentiation medium with different concentrations of leucine for 8 h, followed by western blot analysis. MyoD densitometry values were adjusted to GAPDH intensity and then normalized to expression from the control group (0 mM leucine); (D) Confluent primary satellite cells were cultured in differentiation medium with different concentrations of leucine for 3 days, followed by Western analysis. Myogenin densitometry values were adjusted to GAPDH intensity and then normalized to expression from the control group (0 mM leucine). * p < 0.05, ** p < 0.01, *** p < 0.01 vs. control (0 mM leucine). # p < 0.05, ## p < 0.01 vs. 2.0 mM leucine. All data are shown as the mean ± SD of three independent experiments and representative images are shown.
Nutrients 17 03554 g005
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MDPI and ACS Style

Dai, J.-M.; Yu, M.-X.; Shen, Z.-Y.; Guo, C.-Y.; Zhuang, S.-Q.; Qiu, X.-S. Correction: Dai et al. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400. Nutrients 2025, 17, 3554. https://doi.org/10.3390/nu17223554

AMA Style

Dai J-M, Yu M-X, Shen Z-Y, Guo C-Y, Zhuang S-Q, Qiu X-S. Correction: Dai et al. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400. Nutrients. 2025; 17(22):3554. https://doi.org/10.3390/nu17223554

Chicago/Turabian Style

Dai, Jie-Min, Mu-Xue Yu, Zhen-Yu Shen, Chu-Yi Guo, Si-Qi Zhuang, and Xiao-Shan Qiu. 2025. "Correction: Dai et al. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400" Nutrients 17, no. 22: 3554. https://doi.org/10.3390/nu17223554

APA Style

Dai, J.-M., Yu, M.-X., Shen, Z.-Y., Guo, C.-Y., Zhuang, S.-Q., & Qiu, X.-S. (2025). Correction: Dai et al. Leucine Promotes Proliferation and Differentiation of Primary Preterm Rat Satellite Cells in Part through mTORC1 Signaling Pathway. Nutrients 2015, 7, 3387–3400. Nutrients, 17(22), 3554. https://doi.org/10.3390/nu17223554

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