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Synapse
February 2, 2026Cells0 citationsOpen Access

Correction: Xu et al. Notch1 Protects Against Ischemic-Reperfusion Injury by Suppressing PTEN-Pink1-Mediated Mitochondrial Dysfunction and Mitophagy. Cells 2023, 12, 137

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QXQirong XuSLSheng LiuQGQiang Gong

Key Points

  • The research focuses on understanding how Notch1 protects cells from ischemic-reperfusion injury by affecting mitochondrial functions.
  • Examined the role of Notch1 in cellular responses to ischemic-reperfusion injury.
  • Analyzed mitochondrial dysfunction using various biochemical assays.
  • Investigated the relationship between PTEN, Pink1, and mitochondrial health in the context of Notch1 signaling.
  • Notch1 activation significantly reduces the severity of ischemic-reperfusion injury.
  • Inhibition of PTEN enhances Pink1 activity, improving mitochondrial function.
  • Cells with activated Notch1 showed lower levels of mitophagy markers compared to controls.

Abstract

In the original publication ...

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Cite This Study

Xu et al. (2026) studied this question.

synapsesocial.com/papers/6980fe8ac1c9540dea810ab3https://doi.org/10.3390/cells15030262
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Notch signaling activation contributes to cardioprotection provided by ischemic preconditioning and postconditioning2013 · 64 citations
  2. 2Notch1 protectives against ischemic reperfusion injury via suppressing PTEN-Pink1 mediated mitochondrial dysfunction and mitophagy2022 · 2 citations
  3. 3Notch1 protectives against ischemic reperfusion injury via suppressing PTEN-Pink1 mediated mitochondrial dysfunction and mitophagy2022 · 2 citations
  4. 4Control of cardiac jelly dynamics by NOTCH1 and NRG1 defines the building plan for trabeculation2018 · 224 citations
  5. 5A novel cardioprotective function for DRP1 inhibition2021 · 3 citations