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PUMA- and Bax-induced autophagy contributes to apoptosis

Open access
Yee, K S, Wilkinson, S, James, J, Ryan, K M, Vousden, K H·2009·Cell Death & Differentiation

Abstract

The p53-inducible BH3-only protein PUMA is a key mediator of p53-dependent apoptosis, and PUMA has been shown to function by activating Bax and mitochondrial outer membrane permeabilization. In this study, we describe an ability of PUMA to induce autophagy that leads to the selective removal of mitochondria. This function of PUMA depends on Bax/Bak and can be reproduced by overexpression of Bax. The induction of autophagy coincides with cytochrome c release, and taken together the results suggest that PUMA functions through Bax to induce mitochondrial autophagy in response to mitochondrial perturbations. Surprisingly, inhibition of PUMA or Bax-induced autophagy dampens the apoptotic response, suggesting that under some circumstances the selective targeting of mitochondria for autophagy can enhance apoptosis.

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Crossref · 10.1038/cdd.2009.28

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Metadata

Authors
Yee, K. S., Wilkinson, S., James, J., Ryan, K. M., & Vousden, K. H.
Venue
Cell Death & Differentiation
Published
2009-03-20
Volume
16
Issue
8
Pages
1135-1145
ISSN
  • 1350-9047 (ISSN-L)
  • 1476-5403
OpenAlex
W1969370465
Cited by
236
References
12
FWCI
15.01
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: PUMA- and Bax-induced autophagy contributes to apoptosis. https://app.cochat.ai/papers/10.1038/cdd.2009.28
The paper
Yee, K. S., Wilkinson, S., James, J., Ryan, K. M., & Vousden, K. H. (2009). PUMA- and Bax-induced autophagy contributes to apoptosis. Cell Death & Differentiation. https://doi.org/10.1038/cdd.2009.28

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.