1. Cysteine 202 of cyclophilin D is a site of multiple post-translational modifications and plays a role in cardioprotection.
- Author
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Amanakis G, Sun J, Fergusson MM, McGinty S, Liu C, Molkentin JD, and Murphy E
- Subjects
- Acetylation, Animals, Calcium metabolism, Peptidyl-Prolyl Isomerase F genetics, Cysteine, Disease Models, Animal, Isolated Heart Preparation, Mice, Inbred C57BL, Mice, Transgenic, Mitochondria, Heart pathology, Mutation, Myocardial Infarction enzymology, Myocardial Infarction genetics, Myocardial Infarction pathology, Myocardial Reperfusion Injury enzymology, Myocardial Reperfusion Injury genetics, Myocardial Reperfusion Injury pathology, Myocytes, Cardiac pathology, Oxidation-Reduction, Oxidative Stress, Mice, Peptidyl-Prolyl Isomerase F metabolism, Mitochondria, Heart metabolism, Mitochondrial Permeability Transition Pore metabolism, Myocardial Infarction prevention & control, Myocardial Reperfusion Injury prevention & control, Myocytes, Cardiac enzymology, Protein Processing, Post-Translational
- Abstract
Aims: Cyclophilin-D is a well-known regulator of the mitochondrial permeability transition pore (PTP), the main effector of cardiac ischaemia/reperfusion injury. However, the binding of CypD to the PTP is poorly understood. Cysteine 202 (C202) of CypD is highly conserved among species and can undergo redox-sensitive post-translational modifications. We investigated whether C202 regulates the opening of PTP., Methods and Results: We developed a knock-in mouse model using CRISPR where CypD-C202 was mutated to a serine (C202S). Infarct size is reduced in CypD-C202S Langendorff perfused hearts compared to wild type (WT). Cardiac mitochondria from CypD-C202S mice also have higher calcium retention capacity compared to WT. Therefore, we hypothesized that oxidation of C202 might target CypD to the PTP. Indeed, isolated cardiac mitochondria subjected to oxidative stress exhibit less binding of CypD-C202S to the proposed PTP component F1F0-ATP-synthase. We previously found C202 to be S-nitrosylated in ischaemic preconditioning. Cysteine residues can also undergo S-acylation, and C202 matched an S-acylation motif. S-acylation of CypD-C202 was assessed using a resin-assisted capture (Acyl-RAC). WT hearts are abundantly S-acylated on CypD C202 under baseline conditions indicating that S-acylation on C202 per se does not lead to PTP opening. CypD C202S knock-in hearts are protected from ischaemia/reperfusion injury suggesting further that lack of CypD S-acylation at C202 is not detrimental (when C is mutated to S) and does not induce PTP opening. However, we find that ischaemia leads to de-acylation of C202 and that calcium overload in isolated mitochondria promotes de-acylation of CypD. Furthermore, a high bolus of calcium in WT cardiac mitochondria displaces CypD from its physiological binding partners and possibly renders it available for interaction with the PTP., Conclusions: Taken together the data suggest that with ischaemia CypD is de-acylated at C202 allowing the free cysteine residue to undergo oxidation during the first minutes of reperfusion which in turn targets it to the PTP., (Published by Oxford University Press on behalf of the European Society of Cardiology 2020. This work is written by US Government employees and is in the public domain in the US.)
- Published
- 2021
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