Perinuclear mitochondrial clustering for mesenchymal-to-epithelial transition in pluripotency induction

Remodeled mitochondria are characteristic of pluripotent stem cells. However, a role for mitochondrial movement and distribution in pluripotency remains unknown. Here, we show that mitochondrial retrograde transport-mediated perinuclear clustering via dynein complex occurs at the early phase of pluripotency induction. Interestingly, this mitochondrial redistribution is regulated by Yamanaka factor OCT4 but not SOX2 or KLF4. This mitochondrial redistribution, which has effect on the efficiency of somatic cell reprogramming, also depends on DRP1-mediated mitochondrial fission. Importantly, perinuclear mitochondrial clustering is required for mesenchymal-to-epithelial transition (MET), an early step in reprogramming, during which β-catenin regulates the MET process. Furthermore, sufficient amount of β-catenin plays a key role in maintaining stabilization of E-CADHERIN. Taken together, these studies show that perinuclear mitochondrial clustering is an essential organellar step for MET process of pluripotency induction, which may shed light on the subcellular relationship between mitochondrial dynamics, pluripotency, and cellular morphology.

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Publication Details

Journal
Stem Cell Reports
Published
2025-04-17
DOI
https://doi.org/10.1016/j.stemcr.2025.102474
Citations
2
Primary Topic
Pluripotent Stem Cells Research
Type
article
Field-Weighted Citation Impact
1.61
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article

Perinuclear mitochondrial clustering for mesenchymal-to-epithelial transition in pluripotency induction

Shuai Zhou, Shanshan Dong, Zhongfu Ying, Feixiang Bao et al.
2 citations
Stem Cell Reports
Pluripotent Stem Cells Research
1.61
article

Perinuclear mitochondrial clustering for mesenchymal-to-epithelial transition in pluripotency induction

Shuai Zhou, Shanshan Dong, Zhongfu Ying, Feixiang Bao, Xingguo Liu, Qi Long, Hao Yuan, Xiang Ge, Yi Wu, Dajiang Qin, Keshi Chen, Zebin Yuan, Linpeng Li, Zihuang Liu, Yile Huang, Wei Li, Junwei Wang, Yongqiang Chen, Zhi‐Hong Zheng, Liang Yang, Wei Xie, Doris Lin, Yingzhe Ding, H. Qin, Yang Liu
article en
2 citations

Abstract

Remodeled mitochondria are characteristic of pluripotent stem cells. However, a role for mitochondrial movement and distribution in pluripotency remains unknown. Here, we show that mitochondrial retrograde transport-mediated perinuclear clustering via dynein complex occurs at the early phase of pluripotency induction. Interestingly, this mitochondrial redistribution is regulated by Yamanaka factor OCT4 but not SOX2 or KLF4. This mitochondrial redistribution, which has effect on the efficiency of somatic cell reprogramming, also depends on DRP1-mediated mitochondrial fission. Importantly, perinuclear mitochondrial clustering is required for mesenchymal-to-epithelial transition (MET), an early step in reprogramming, during which β-catenin regulates the MET process. Furthermore, sufficient amount of β-catenin plays a key role in maintaining stabilization of E-CADHERIN. Taken together, these studies show that perinuclear mitochondrial clustering is an essential organellar step for MET process of pluripotency induction, which may shed light on the subcellular relationship between mitochondrial dynamics, pluripotency, and cellular morphology.

Stem Cell ReportsVol. 20(5)
Chinese Academy of Sciences (CN), University of Hong Kong (HK), Guangzhou Medical University (CN)
Zero hunger
Openalex Percentile: Top 18%
Pluripotent Stem Cells Research
1.61
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