Correction to: Cell Research (2018) 0:1–16. https://doi.org/10.1038/s41422-018-0056-0; Published online 22 June 2018.

We apologize for three errors that we just found in the paper published online on 22 June 2018. Figure 2b was inadvertently duplicated from Supplementary information, Figure S3d. The PTEN-L/PTEN blot in Fig. 4b was inadvertently cropped. The scale bars of ZOOM channel in Supplementary information, Figure S1f and i, were inadvertently indicated. The corrected version of Figs. 2b and 4b, and the corrected legends of Supplementary information, Figure S1f and i, are provided below. No conclusion was affected by these errors, but we apologize for not detecting them before publication and any inconvenience caused.

Fig. 2
figure 2

PTEN-L negatively regulates mitophagy induced by various mitochondria-damaging agents. b Quantification of mitochondrial proteins from a

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Fig. 4
figure 4

PTEN-L impairs Parkin E3 ligase activity and reduces pSer65-Parkin. b YFP-Parkin-HeLa cells with PTEN-L stable expression or control vector were treated with O/A (10 nM and 100 nM) for indicated hours and the WCLs were analyzed by immunoblotting as indicated

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Figure S1 PTEN-L resides at the outer mitochondrial membrane. f Co-localization of Flag-PTEN-L with Tom20 without or with CCCP (5 µM, 4 h treatment) was examined by confocal fluorescence microscopy. Flag-PTEN-L (Green); Tom20 (Red); co-localization channel (White). Scale bars, 5 and 2 µm (ZOOM). i Co-localization of Flag-PTEN-L with Calreticulin. Flag-PTEN-L (Green); Calreticulin (Red); co-localization channel (White). Scale bars, 5 and 2 µm (ZOOM).